Please choose an event type to view the corresponding MedsFacts report:

NAUSEA ( 2869 FDA reports)
ANXIETY ( 2714 FDA reports)
PAIN ( 2399 FDA reports)
FATIGUE ( 2294 FDA reports)
DYSPNOEA ( 2268 FDA reports)
VOMITING ( 2120 FDA reports)
DIARRHOEA ( 2056 FDA reports)
DEPRESSION ( 2049 FDA reports)
DIZZINESS ( 1915 FDA reports)
FALL ( 1873 FDA reports)
ASTHENIA ( 1759 FDA reports)
HEADACHE ( 1716 FDA reports)
INSOMNIA ( 1497 FDA reports)
PYREXIA ( 1490 FDA reports)
PNEUMONIA ( 1437 FDA reports)
ANAEMIA ( 1394 FDA reports)
BACK PAIN ( 1365 FDA reports)
DRUG INTERACTION ( 1353 FDA reports)
DRUG INEFFECTIVE ( 1347 FDA reports)
HYPERTENSION ( 1334 FDA reports)
SOMNOLENCE ( 1310 FDA reports)
CONFUSIONAL STATE ( 1296 FDA reports)
CONSTIPATION ( 1274 FDA reports)
HYPOTENSION ( 1250 FDA reports)
DEHYDRATION ( 1218 FDA reports)
ABDOMINAL PAIN ( 1205 FDA reports)
ARTHRALGIA ( 1191 FDA reports)
PAIN IN EXTREMITY ( 1191 FDA reports)
CHEST PAIN ( 1164 FDA reports)
COMPLETED SUICIDE ( 1163 FDA reports)
OEDEMA PERIPHERAL ( 1129 FDA reports)
MALAISE ( 1128 FDA reports)
WEIGHT DECREASED ( 1106 FDA reports)
TREMOR ( 1046 FDA reports)
AGITATION ( 1025 FDA reports)
SUICIDE ATTEMPT ( 1009 FDA reports)
CONVULSION ( 997 FDA reports)
WEIGHT INCREASED ( 924 FDA reports)
DEATH ( 921 FDA reports)
HYPOAESTHESIA ( 874 FDA reports)
TACHYCARDIA ( 869 FDA reports)
URINARY TRACT INFECTION ( 851 FDA reports)
INJURY ( 851 FDA reports)
CONDITION AGGRAVATED ( 850 FDA reports)
LOSS OF CONSCIOUSNESS ( 848 FDA reports)
DIABETES MELLITUS ( 841 FDA reports)
RENAL FAILURE ( 840 FDA reports)
GAIT DISTURBANCE ( 839 FDA reports)
RASH ( 832 FDA reports)
RENAL FAILURE ACUTE ( 830 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 815 FDA reports)
SUICIDAL IDEATION ( 810 FDA reports)
OVERDOSE ( 805 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 796 FDA reports)
PARAESTHESIA ( 778 FDA reports)
SYNCOPE ( 751 FDA reports)
MYOCARDIAL INFARCTION ( 747 FDA reports)
OSTEONECROSIS OF JAW ( 741 FDA reports)
FEELING ABNORMAL ( 740 FDA reports)
PULMONARY EMBOLISM ( 739 FDA reports)
DECREASED APPETITE ( 732 FDA reports)
DYSPHAGIA ( 727 FDA reports)
RESPIRATORY FAILURE ( 703 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 698 FDA reports)
NEUTROPENIA ( 698 FDA reports)
PLEURAL EFFUSION ( 679 FDA reports)
CARDIAC ARREST ( 674 FDA reports)
PRURITUS ( 660 FDA reports)
THROMBOCYTOPENIA ( 658 FDA reports)
HYPERHIDROSIS ( 649 FDA reports)
HAEMOGLOBIN DECREASED ( 645 FDA reports)
HYPONATRAEMIA ( 643 FDA reports)
MUSCLE SPASMS ( 639 FDA reports)
DEEP VEIN THROMBOSIS ( 628 FDA reports)
ABDOMINAL PAIN UPPER ( 623 FDA reports)
CEREBROVASCULAR ACCIDENT ( 617 FDA reports)
COUGH ( 614 FDA reports)
NEUROPATHY PERIPHERAL ( 612 FDA reports)
ATRIAL FIBRILLATION ( 603 FDA reports)
EMOTIONAL DISTRESS ( 603 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 594 FDA reports)
VISION BLURRED ( 593 FDA reports)
SEPSIS ( 592 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 592 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 592 FDA reports)
PALPITATIONS ( 573 FDA reports)
MYALGIA ( 561 FDA reports)
BLOOD GLUCOSE INCREASED ( 550 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 545 FDA reports)
BRONCHITIS ( 541 FDA reports)
BONE DISORDER ( 536 FDA reports)
OSTEOARTHRITIS ( 530 FDA reports)
TYPE 2 DIABETES MELLITUS ( 526 FDA reports)
BLOOD PRESSURE INCREASED ( 524 FDA reports)
PAIN IN JAW ( 524 FDA reports)
DELIRIUM ( 519 FDA reports)
INFECTION ( 518 FDA reports)
INTENTIONAL OVERDOSE ( 511 FDA reports)
COMA ( 508 FDA reports)
HYPOKALAEMIA ( 499 FDA reports)
CHILLS ( 488 FDA reports)
PSYCHOTIC DISORDER ( 480 FDA reports)
LEUKOPENIA ( 479 FDA reports)
CONTUSION ( 478 FDA reports)
CELLULITIS ( 474 FDA reports)
AMNESIA ( 467 FDA reports)
BLOOD CREATININE INCREASED ( 458 FDA reports)
MENTAL STATUS CHANGES ( 457 FDA reports)
HEART RATE INCREASED ( 448 FDA reports)
PANCYTOPENIA ( 447 FDA reports)
MEMORY IMPAIRMENT ( 446 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 445 FDA reports)
OSTEOMYELITIS ( 442 FDA reports)
DISORIENTATION ( 439 FDA reports)
AGGRESSION ( 438 FDA reports)
BONE PAIN ( 437 FDA reports)
CORONARY ARTERY DISEASE ( 437 FDA reports)
FEBRILE NEUTROPENIA ( 428 FDA reports)
HALLUCINATION ( 426 FDA reports)
RESTLESSNESS ( 423 FDA reports)
PLATELET COUNT DECREASED ( 415 FDA reports)
DYSPEPSIA ( 415 FDA reports)
OEDEMA ( 410 FDA reports)
ANHEDONIA ( 409 FDA reports)
IMPAIRED HEALING ( 406 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 405 FDA reports)
MUSCULAR WEAKNESS ( 401 FDA reports)
BRADYCARDIA ( 400 FDA reports)
RESPIRATORY ARREST ( 399 FDA reports)
ATELECTASIS ( 397 FDA reports)
LETHARGY ( 397 FDA reports)
CHOLELITHIASIS ( 394 FDA reports)
ERYTHEMA ( 394 FDA reports)
SPINAL OSTEOARTHRITIS ( 394 FDA reports)
SINUSITIS ( 392 FDA reports)
SLEEP DISORDER ( 392 FDA reports)
DISTURBANCE IN ATTENTION ( 392 FDA reports)
BALANCE DISORDER ( 390 FDA reports)
DRUG TOXICITY ( 388 FDA reports)
ABDOMINAL DISTENSION ( 387 FDA reports)
CARDIO-RESPIRATORY ARREST ( 386 FDA reports)
HYPERLIPIDAEMIA ( 386 FDA reports)
NECK PAIN ( 382 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 380 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 379 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 379 FDA reports)
TOOTH EXTRACTION ( 371 FDA reports)
IRRITABILITY ( 370 FDA reports)
DYSARTHRIA ( 369 FDA reports)
OSTEONECROSIS ( 368 FDA reports)
NERVOUSNESS ( 365 FDA reports)
HYPOXIA ( 364 FDA reports)
SWELLING ( 361 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 360 FDA reports)
MUSCULOSKELETAL PAIN ( 360 FDA reports)
CHEST DISCOMFORT ( 359 FDA reports)
SEDATION ( 358 FDA reports)
HYPERGLYCAEMIA ( 357 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 353 FDA reports)
SPEECH DISORDER ( 349 FDA reports)
DRUG DEPENDENCE ( 345 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 345 FDA reports)
PULMONARY OEDEMA ( 342 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 341 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 339 FDA reports)
DYSKINESIA ( 337 FDA reports)
ABDOMINAL DISCOMFORT ( 335 FDA reports)
RHABDOMYOLYSIS ( 334 FDA reports)
METASTASES TO BONE ( 324 FDA reports)
SINUS TACHYCARDIA ( 323 FDA reports)
DYSURIA ( 322 FDA reports)
NEOPLASM MALIGNANT ( 322 FDA reports)
CATARACT ( 321 FDA reports)
PANCREATITIS ( 321 FDA reports)
DISEASE PROGRESSION ( 315 FDA reports)
DENTAL CARIES ( 314 FDA reports)
CARDIAC DISORDER ( 312 FDA reports)
STRESS ( 312 FDA reports)
ABNORMAL BEHAVIOUR ( 311 FDA reports)
DRY MOUTH ( 309 FDA reports)
ARTHRITIS ( 308 FDA reports)
UNRESPONSIVE TO STIMULI ( 308 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 307 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 307 FDA reports)
URINARY RETENTION ( 305 FDA reports)
SWELLING FACE ( 304 FDA reports)
RENAL FAILURE CHRONIC ( 302 FDA reports)
CARDIOMEGALY ( 302 FDA reports)
HAEMATOCRIT DECREASED ( 302 FDA reports)
VISUAL IMPAIRMENT ( 294 FDA reports)
MENTAL DISORDER ( 293 FDA reports)
HYPOPHAGIA ( 292 FDA reports)
PANIC ATTACK ( 292 FDA reports)
TREATMENT NONCOMPLIANCE ( 291 FDA reports)
VERTIGO ( 288 FDA reports)
GASTRITIS ( 286 FDA reports)
OSTEOPOROSIS ( 286 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 284 FDA reports)
FLUSHING ( 282 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 282 FDA reports)
HAEMORRHAGE ( 281 FDA reports)
ALOPECIA ( 277 FDA reports)
DECREASED INTEREST ( 277 FDA reports)
OSTEOPENIA ( 276 FDA reports)
CARDIAC FAILURE ( 275 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 272 FDA reports)
TOOTHACHE ( 270 FDA reports)
BLOOD PRESSURE DECREASED ( 269 FDA reports)
HYPERSENSITIVITY ( 268 FDA reports)
URINARY INCONTINENCE ( 268 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 267 FDA reports)
BLOOD SODIUM DECREASED ( 266 FDA reports)
PNEUMONIA ASPIRATION ( 266 FDA reports)
CRYING ( 265 FDA reports)
HEPATIC STEATOSIS ( 265 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 264 FDA reports)
LYMPHADENOPATHY ( 264 FDA reports)
ENCEPHALOPATHY ( 263 FDA reports)
URTICARIA ( 263 FDA reports)
SEPTIC SHOCK ( 260 FDA reports)
HEART RATE IRREGULAR ( 259 FDA reports)
ASTHMA ( 257 FDA reports)
MITRAL VALVE INCOMPETENCE ( 256 FDA reports)
LEUKOCYTOSIS ( 252 FDA reports)
OBESITY ( 252 FDA reports)
RECTAL HAEMORRHAGE ( 252 FDA reports)
TINNITUS ( 251 FDA reports)
DEFORMITY ( 251 FDA reports)
ASCITES ( 250 FDA reports)
MIGRAINE ( 250 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 249 FDA reports)
HOT FLUSH ( 247 FDA reports)
MUCOSAL INFLAMMATION ( 247 FDA reports)
OFF LABEL USE ( 247 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 246 FDA reports)
FEAR ( 244 FDA reports)
HERPES ZOSTER ( 244 FDA reports)
RENAL IMPAIRMENT ( 243 FDA reports)
RESPIRATORY DISTRESS ( 242 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 242 FDA reports)
MULTI-ORGAN FAILURE ( 242 FDA reports)
COGNITIVE DISORDER ( 241 FDA reports)
SEROTONIN SYNDROME ( 241 FDA reports)
SLEEP APNOEA SYNDROME ( 241 FDA reports)
EPISTAXIS ( 240 FDA reports)
INCORRECT DOSE ADMINISTERED ( 240 FDA reports)
HAEMATURIA ( 239 FDA reports)
ARRHYTHMIA ( 237 FDA reports)
INFLAMMATION ( 235 FDA reports)
DRUG DOSE OMISSION ( 233 FDA reports)
METABOLIC ACIDOSIS ( 233 FDA reports)
METASTASES TO LIVER ( 233 FDA reports)
STAPHYLOCOCCAL INFECTION ( 231 FDA reports)
ROAD TRAFFIC ACCIDENT ( 230 FDA reports)
THROMBOSIS ( 230 FDA reports)
ANOREXIA ( 229 FDA reports)
DEPRESSED MOOD ( 229 FDA reports)
HAEMATOCHEZIA ( 229 FDA reports)
ECONOMIC PROBLEM ( 228 FDA reports)
GRAND MAL CONVULSION ( 226 FDA reports)
MULTIPLE DRUG OVERDOSE ( 226 FDA reports)
HAEMORRHOIDS ( 225 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 224 FDA reports)
BONE LESION ( 223 FDA reports)
ORAL PAIN ( 220 FDA reports)
DYSPNOEA EXERTIONAL ( 219 FDA reports)
MEDICATION ERROR ( 219 FDA reports)
POISONING ( 219 FDA reports)
POLLAKIURIA ( 219 FDA reports)
RENAL CYST ( 219 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 219 FDA reports)
BLOOD POTASSIUM DECREASED ( 218 FDA reports)
HALLUCINATION, AUDITORY ( 218 FDA reports)
HYPERKALAEMIA ( 217 FDA reports)
OXYGEN SATURATION DECREASED ( 217 FDA reports)
WHEEZING ( 217 FDA reports)
JOINT SWELLING ( 216 FDA reports)
DRUG EFFECT DECREASED ( 215 FDA reports)
NIGHTMARE ( 214 FDA reports)
DYSGEUSIA ( 213 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 212 FDA reports)
HYPOGLYCAEMIA ( 211 FDA reports)
MULTIPLE MYELOMA ( 211 FDA reports)
CARDIOMYOPATHY ( 208 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 207 FDA reports)
LUNG INFILTRATION ( 207 FDA reports)
DIVERTICULUM ( 205 FDA reports)
NEPHROLITHIASIS ( 205 FDA reports)
HEPATIC FAILURE ( 201 FDA reports)
HEAD INJURY ( 200 FDA reports)
HIATUS HERNIA ( 199 FDA reports)
HYPOTHYROIDISM ( 199 FDA reports)
STOMATITIS ( 199 FDA reports)
ASPIRATION ( 198 FDA reports)
DELUSION ( 198 FDA reports)
PARANOIA ( 198 FDA reports)
ANGINA PECTORIS ( 195 FDA reports)
BLOOD BILIRUBIN INCREASED ( 195 FDA reports)
NEUTROPHIL COUNT DECREASED ( 195 FDA reports)
OROPHARYNGEAL PAIN ( 195 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 194 FDA reports)
HEPATIC ENZYME INCREASED ( 194 FDA reports)
INFLUENZA ( 194 FDA reports)
INFLUENZA LIKE ILLNESS ( 194 FDA reports)
CANDIDIASIS ( 193 FDA reports)
DRUG HYPERSENSITIVITY ( 193 FDA reports)
RIB FRACTURE ( 193 FDA reports)
SCHIZOPHRENIA ( 193 FDA reports)
UNEVALUABLE EVENT ( 193 FDA reports)
TOOTH DISORDER ( 191 FDA reports)
CARDIAC MURMUR ( 189 FDA reports)
LUNG NEOPLASM ( 189 FDA reports)
HAEMATOMA ( 187 FDA reports)
NASOPHARYNGITIS ( 187 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 186 FDA reports)
MOUTH ULCERATION ( 186 FDA reports)
LUNG DISORDER ( 185 FDA reports)
ARTERIOSCLEROSIS ( 184 FDA reports)
EMPHYSEMA ( 184 FDA reports)
MALNUTRITION ( 184 FDA reports)
RESTLESS LEGS SYNDROME ( 184 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 183 FDA reports)
LIVER DISORDER ( 183 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 182 FDA reports)
FLATULENCE ( 181 FDA reports)
ABASIA ( 180 FDA reports)
BURNING SENSATION ( 180 FDA reports)
HAEMATEMESIS ( 179 FDA reports)
MANIA ( 179 FDA reports)
MUSCLE RIGIDITY ( 179 FDA reports)
SCOLIOSIS ( 179 FDA reports)
AKATHISIA ( 177 FDA reports)
DRUG ABUSE ( 177 FDA reports)
PULMONARY HYPERTENSION ( 176 FDA reports)
TOOTH LOSS ( 175 FDA reports)
TARDIVE DYSKINESIA ( 174 FDA reports)
ANGER ( 174 FDA reports)
EMOTIONAL DISORDER ( 173 FDA reports)
COLITIS ( 172 FDA reports)
RHINORRHOEA ( 172 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 171 FDA reports)
CATATONIA ( 171 FDA reports)
BLINDNESS ( 170 FDA reports)
BLOOD UREA INCREASED ( 170 FDA reports)
MACULAR DEGENERATION ( 170 FDA reports)
NERVOUS SYSTEM DISORDER ( 170 FDA reports)
HYPERSOMNIA ( 169 FDA reports)
SURGERY ( 169 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 168 FDA reports)
EYE PAIN ( 168 FDA reports)
CYANOSIS ( 167 FDA reports)
APHASIA ( 166 FDA reports)
DRUG LEVEL INCREASED ( 165 FDA reports)
PANCREATITIS ACUTE ( 165 FDA reports)
DEMENTIA ( 164 FDA reports)
EAR PAIN ( 164 FDA reports)
INJECTION SITE PAIN ( 164 FDA reports)
INTENTIONAL DRUG MISUSE ( 164 FDA reports)
WITHDRAWAL SYNDROME ( 164 FDA reports)
PRODUCTIVE COUGH ( 162 FDA reports)
DYSPHONIA ( 162 FDA reports)
DECUBITUS ULCER ( 160 FDA reports)
METASTASES TO SPINE ( 160 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 160 FDA reports)
VENTRICULAR TACHYCARDIA ( 160 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 159 FDA reports)
INTERSTITIAL LUNG DISEASE ( 159 FDA reports)
HALLUCINATION, VISUAL ( 158 FDA reports)
HIP FRACTURE ( 158 FDA reports)
PULMONARY CONGESTION ( 157 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 155 FDA reports)
FUNGAL INFECTION ( 155 FDA reports)
OESOPHAGITIS ( 155 FDA reports)
DISCOMFORT ( 154 FDA reports)
BURSITIS ( 153 FDA reports)
DIABETIC NEUROPATHY ( 153 FDA reports)
ILL-DEFINED DISORDER ( 153 FDA reports)
LUMBAR SPINAL STENOSIS ( 153 FDA reports)
NASAL CONGESTION ( 153 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 152 FDA reports)
ERECTILE DYSFUNCTION ( 152 FDA reports)
ABNORMAL DREAMS ( 151 FDA reports)
CIRCULATORY COLLAPSE ( 151 FDA reports)
NIGHT SWEATS ( 151 FDA reports)
RENAL DISORDER ( 151 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 151 FDA reports)
ARTHROPATHY ( 150 FDA reports)
DYSTONIA ( 150 FDA reports)
GASTROINTESTINAL DISORDER ( 150 FDA reports)
RASH PRURITIC ( 149 FDA reports)
CYSTITIS ( 148 FDA reports)
ORAL CANDIDIASIS ( 148 FDA reports)
CEREBRAL ATROPHY ( 147 FDA reports)
EXOSTOSIS ( 147 FDA reports)
LOOSE TOOTH ( 147 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 147 FDA reports)
SKIN DISCOLOURATION ( 147 FDA reports)
SPINAL COLUMN STENOSIS ( 146 FDA reports)
PROTHROMBIN TIME PROLONGED ( 145 FDA reports)
DIPLOPIA ( 145 FDA reports)
GASTROENTERITIS ( 145 FDA reports)
HYPERCHOLESTEROLAEMIA ( 145 FDA reports)
GALLBLADDER DISORDER ( 144 FDA reports)
FEELING HOT ( 142 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 142 FDA reports)
SINUS DISORDER ( 141 FDA reports)
BIPOLAR DISORDER ( 141 FDA reports)
GINGIVAL PAIN ( 140 FDA reports)
MOOD SWINGS ( 140 FDA reports)
PRESYNCOPE ( 140 FDA reports)
TOOTH INFECTION ( 140 FDA reports)
RASH GENERALISED ( 139 FDA reports)
THINKING ABNORMAL ( 139 FDA reports)
CHOLECYSTITIS CHRONIC ( 139 FDA reports)
MOVEMENT DISORDER ( 138 FDA reports)
CHRONIC SINUSITIS ( 137 FDA reports)
EATING DISORDER ( 137 FDA reports)
FLUID RETENTION ( 137 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 137 FDA reports)
SCAR ( 137 FDA reports)
TOOTH FRACTURE ( 137 FDA reports)
SWOLLEN TONGUE ( 136 FDA reports)
AGRANULOCYTOSIS ( 136 FDA reports)
COORDINATION ABNORMAL ( 136 FDA reports)
OSTEOLYSIS ( 136 FDA reports)
HAEMOPTYSIS ( 135 FDA reports)
HOSPITALISATION ( 135 FDA reports)
RADIOTHERAPY ( 135 FDA reports)
SKIN ULCER ( 135 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 135 FDA reports)
BLISTER ( 134 FDA reports)
INCONTINENCE ( 134 FDA reports)
ORTHOSTATIC HYPOTENSION ( 134 FDA reports)
ACCIDENTAL OVERDOSE ( 133 FDA reports)
ACUTE RESPIRATORY FAILURE ( 133 FDA reports)
ATAXIA ( 133 FDA reports)
HYPOMAGNESAEMIA ( 133 FDA reports)
MENTAL IMPAIRMENT ( 133 FDA reports)
PERICARDIAL EFFUSION ( 132 FDA reports)
SOPOR ( 132 FDA reports)
PARKINSONISM ( 131 FDA reports)
MELAENA ( 131 FDA reports)
MYOCARDIAL ISCHAEMIA ( 131 FDA reports)
CHOLECYSTITIS ( 130 FDA reports)
NEOPLASM PROGRESSION ( 130 FDA reports)
PRODUCT QUALITY ISSUE ( 130 FDA reports)
STEVENS-JOHNSON SYNDROME ( 129 FDA reports)
DEAFNESS ( 129 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 129 FDA reports)
FIBROMYALGIA ( 129 FDA reports)
MYDRIASIS ( 129 FDA reports)
DIVERTICULITIS ( 128 FDA reports)
DYSSTASIA ( 128 FDA reports)
EXPOSED BONE IN JAW ( 128 FDA reports)
HEPATIC CYST ( 128 FDA reports)
NEURALGIA ( 128 FDA reports)
PALLOR ( 128 FDA reports)
STATUS EPILEPTICUS ( 128 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 127 FDA reports)
BREAST CANCER ( 127 FDA reports)
CEREBRAL INFARCTION ( 127 FDA reports)
FEELING JITTERY ( 127 FDA reports)
JAUNDICE ( 127 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 126 FDA reports)
COMPRESSION FRACTURE ( 125 FDA reports)
PURULENT DISCHARGE ( 125 FDA reports)
RESPIRATORY DEPRESSION ( 125 FDA reports)
TOOTH ABSCESS ( 125 FDA reports)
FISTULA ( 124 FDA reports)
GINGIVAL SWELLING ( 124 FDA reports)
GLAUCOMA ( 124 FDA reports)
INTENTIONAL SELF-INJURY ( 124 FDA reports)
MULTIPLE INJURIES ( 124 FDA reports)
MUSCLE TWITCHING ( 124 FDA reports)
BODY TEMPERATURE INCREASED ( 123 FDA reports)
INTESTINAL OBSTRUCTION ( 123 FDA reports)
HAEMODIALYSIS ( 121 FDA reports)
MYOCLONUS ( 121 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 121 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 121 FDA reports)
BLOOD GLUCOSE DECREASED ( 120 FDA reports)
HEPATOTOXICITY ( 120 FDA reports)
INJECTION SITE ERYTHEMA ( 120 FDA reports)
MASS ( 120 FDA reports)
HEART RATE DECREASED ( 119 FDA reports)
NOCTURIA ( 119 FDA reports)
VISUAL ACUITY REDUCED ( 119 FDA reports)
PRIMARY SEQUESTRUM ( 118 FDA reports)
SPLENOMEGALY ( 118 FDA reports)
DRY EYE ( 118 FDA reports)
LACERATION ( 118 FDA reports)
CEREBRAL HAEMORRHAGE ( 117 FDA reports)
ELECTROLYTE IMBALANCE ( 117 FDA reports)
GRANULOCYTOPENIA ( 117 FDA reports)
LUNG NEOPLASM MALIGNANT ( 117 FDA reports)
MOOD ALTERED ( 117 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 116 FDA reports)
FACIAL PAIN ( 115 FDA reports)
FAILURE TO THRIVE ( 115 FDA reports)
MOBILITY DECREASED ( 115 FDA reports)
PATHOLOGICAL FRACTURE ( 115 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 114 FDA reports)
ECZEMA ( 114 FDA reports)
DRUG ABUSER ( 113 FDA reports)
EJECTION FRACTION DECREASED ( 113 FDA reports)
HEPATITIS ( 113 FDA reports)
RASH ERYTHEMATOUS ( 113 FDA reports)
ROTATOR CUFF SYNDROME ( 113 FDA reports)
SPINAL COMPRESSION FRACTURE ( 113 FDA reports)
VIRAL INFECTION ( 112 FDA reports)
EPILEPSY ( 112 FDA reports)
FEMUR FRACTURE ( 111 FDA reports)
ILEUS ( 111 FDA reports)
SKIN LESION ( 111 FDA reports)
FACE OEDEMA ( 110 FDA reports)
FLUID OVERLOAD ( 110 FDA reports)
HYPOTHERMIA ( 110 FDA reports)
METASTASES TO LUNG ( 110 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 109 FDA reports)
COLONIC POLYP ( 109 FDA reports)
DEBRIDEMENT ( 109 FDA reports)
PHYSICAL DISABILITY ( 109 FDA reports)
PNEUMONITIS ( 109 FDA reports)
AFFECTIVE DISORDER ( 108 FDA reports)
HYPERCALCAEMIA ( 108 FDA reports)
LABILE BLOOD PRESSURE ( 108 FDA reports)
ALCOHOL USE ( 107 FDA reports)
ANGINA UNSTABLE ( 107 FDA reports)
DERMATITIS ( 107 FDA reports)
KYPHOSIS ( 107 FDA reports)
MAJOR DEPRESSION ( 107 FDA reports)
GASTRIC ULCER ( 106 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 106 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 106 FDA reports)
SUDDEN DEATH ( 105 FDA reports)
JOINT STIFFNESS ( 105 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 105 FDA reports)
NO THERAPEUTIC RESPONSE ( 105 FDA reports)
GROIN PAIN ( 104 FDA reports)
RESPIRATORY DISORDER ( 104 FDA reports)
POST PROCEDURAL COMPLICATION ( 103 FDA reports)
RHEUMATOID ARTHRITIS ( 103 FDA reports)
HEART VALVE INCOMPETENCE ( 103 FDA reports)
BRONCHOPNEUMONIA ( 102 FDA reports)
DRY SKIN ( 102 FDA reports)
HEMIPARESIS ( 102 FDA reports)
TENDERNESS ( 102 FDA reports)
SINUS BRADYCARDIA ( 101 FDA reports)
GASTRIC DISORDER ( 101 FDA reports)
HEPATIC LESION ( 101 FDA reports)
HEPATITIS C ( 101 FDA reports)
OSTEOSCLEROSIS ( 101 FDA reports)
BACTERAEMIA ( 100 FDA reports)
HEPATIC CIRRHOSIS ( 100 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 100 FDA reports)
FLANK PAIN ( 99 FDA reports)
HEPATOMEGALY ( 99 FDA reports)
HYDRONEPHROSIS ( 99 FDA reports)
JAW OPERATION ( 99 FDA reports)
THIRST ( 99 FDA reports)
MULTIPLE SCLEROSIS ( 98 FDA reports)
ABSCESS ( 97 FDA reports)
PSORIASIS ( 97 FDA reports)
URINE ODOUR ABNORMAL ( 97 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 96 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 96 FDA reports)
PSYCHIATRIC SYMPTOM ( 95 FDA reports)
RENAL TUBULAR NECROSIS ( 95 FDA reports)
DIABETIC KETOACIDOSIS ( 95 FDA reports)
FAECAL INCONTINENCE ( 95 FDA reports)
COAGULOPATHY ( 94 FDA reports)
DYSLIPIDAEMIA ( 94 FDA reports)
IRRITABLE BOWEL SYNDROME ( 94 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 94 FDA reports)
BRADYPHRENIA ( 93 FDA reports)
HEART VALVE CALCIFICATION ( 93 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 93 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 93 FDA reports)
RASH MACULO-PAPULAR ( 93 FDA reports)
ENDODONTIC PROCEDURE ( 92 FDA reports)
IRON DEFICIENCY ANAEMIA ( 92 FDA reports)
ATRIAL FLUTTER ( 91 FDA reports)
BACTERIAL INFECTION ( 91 FDA reports)
BLOOD URINE PRESENT ( 91 FDA reports)
DRUG ADMINISTRATION ERROR ( 91 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 91 FDA reports)
JOINT EFFUSION ( 91 FDA reports)
TENDONITIS ( 91 FDA reports)
PULMONARY FIBROSIS ( 90 FDA reports)
SUBDURAL HAEMATOMA ( 90 FDA reports)
ANAPHYLACTIC REACTION ( 90 FDA reports)
AORTIC VALVE INCOMPETENCE ( 90 FDA reports)
APATHY ( 90 FDA reports)
LACRIMATION INCREASED ( 90 FDA reports)
LYMPHOEDEMA ( 90 FDA reports)
APNOEA ( 89 FDA reports)
BONE MARROW FAILURE ( 89 FDA reports)
DISABILITY ( 89 FDA reports)
FOOT FRACTURE ( 89 FDA reports)
HYPOVOLAEMIA ( 89 FDA reports)
INCREASED APPETITE ( 89 FDA reports)
NEUTROPHIL COUNT INCREASED ( 89 FDA reports)
ONYCHOMYCOSIS ( 89 FDA reports)
TRANSAMINASES INCREASED ( 89 FDA reports)
SKIN DISORDER ( 88 FDA reports)
WOUND DEHISCENCE ( 88 FDA reports)
BLOOD POTASSIUM INCREASED ( 88 FDA reports)
DEVICE RELATED INFECTION ( 88 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 88 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 88 FDA reports)
OPEN WOUND ( 88 FDA reports)
AORTIC ANEURYSM ( 87 FDA reports)
DRUG INTOLERANCE ( 87 FDA reports)
MICTURITION URGENCY ( 87 FDA reports)
AZOTAEMIA ( 86 FDA reports)
JAW FRACTURE ( 86 FDA reports)
LOBAR PNEUMONIA ( 86 FDA reports)
PERIPHERAL COLDNESS ( 86 FDA reports)
SKIN LACERATION ( 86 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 85 FDA reports)
GINGIVAL INFECTION ( 85 FDA reports)
LOCAL SWELLING ( 85 FDA reports)
MASTICATION DISORDER ( 85 FDA reports)
ACIDOSIS ( 84 FDA reports)
GENERALISED OEDEMA ( 84 FDA reports)
PNEUMOTHORAX ( 84 FDA reports)
SPONDYLOLISTHESIS ( 84 FDA reports)
TACHYPNOEA ( 84 FDA reports)
PELVIC PAIN ( 83 FDA reports)
PRURITUS GENERALISED ( 83 FDA reports)
BASAL CELL CARCINOMA ( 83 FDA reports)
CHROMATURIA ( 83 FDA reports)
DIALYSIS ( 83 FDA reports)
LACTIC ACIDOSIS ( 83 FDA reports)
MIDDLE INSOMNIA ( 83 FDA reports)
PARAESTHESIA ORAL ( 83 FDA reports)
CROHN'S DISEASE ( 82 FDA reports)
JOINT INJURY ( 82 FDA reports)
OTITIS MEDIA ( 82 FDA reports)
PETECHIAE ( 82 FDA reports)
VENOUS INSUFFICIENCY ( 82 FDA reports)
PREGNANCY ( 81 FDA reports)
SQUAMOUS CELL CARCINOMA ( 81 FDA reports)
ULCER ( 81 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 81 FDA reports)
DROOLING ( 81 FDA reports)
HYPERVENTILATION ( 81 FDA reports)
HYPOTONIA ( 81 FDA reports)
BLOOD ALBUMIN DECREASED ( 80 FDA reports)
BLOOD CALCIUM DECREASED ( 80 FDA reports)
COLD SWEAT ( 80 FDA reports)
HYPOAESTHESIA ORAL ( 80 FDA reports)
HYPOCALCAEMIA ( 80 FDA reports)
LIBIDO DECREASED ( 80 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 80 FDA reports)
PERIODONTAL DISEASE ( 80 FDA reports)
RESPIRATORY TRACT INFECTION ( 80 FDA reports)
RHINITIS ( 79 FDA reports)
SALIVARY HYPERSECRETION ( 79 FDA reports)
SCIATICA ( 79 FDA reports)
TYPE 1 DIABETES MELLITUS ( 79 FDA reports)
VAGINAL HAEMORRHAGE ( 79 FDA reports)
CLOSTRIDIAL INFECTION ( 79 FDA reports)
CORONARY ARTERY OCCLUSION ( 79 FDA reports)
DISEASE RECURRENCE ( 79 FDA reports)
INJECTION SITE HAEMORRHAGE ( 79 FDA reports)
LIMB INJURY ( 79 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 78 FDA reports)
GYNAECOMASTIA ( 78 FDA reports)
INTESTINAL PERFORATION ( 78 FDA reports)
JAW DISORDER ( 78 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 78 FDA reports)
OSTEITIS ( 78 FDA reports)
SENSORY DISTURBANCE ( 78 FDA reports)
SHOCK ( 77 FDA reports)
VISUAL DISTURBANCE ( 77 FDA reports)
CHOLESTASIS ( 77 FDA reports)
EAR INFECTION ( 77 FDA reports)
HYPERNATRAEMIA ( 77 FDA reports)
HYPOALBUMINAEMIA ( 77 FDA reports)
ISCHAEMIA ( 77 FDA reports)
CYST ( 76 FDA reports)
METASTASES TO LYMPH NODES ( 76 FDA reports)
PHARYNGITIS ( 76 FDA reports)
RESPIRATORY RATE INCREASED ( 76 FDA reports)
PLATELET COUNT INCREASED ( 75 FDA reports)
TONGUE DISORDER ( 75 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 75 FDA reports)
IMPAIRED DRIVING ABILITY ( 75 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 75 FDA reports)
INFUSION RELATED REACTION ( 75 FDA reports)
MENINGITIS ( 75 FDA reports)
METASTATIC NEOPLASM ( 75 FDA reports)
CAROTID ARTERY STENOSIS ( 74 FDA reports)
DIVERTICULUM INTESTINAL ( 74 FDA reports)
MUSCLE DISORDER ( 74 FDA reports)
ORAL INFECTION ( 74 FDA reports)
THROAT IRRITATION ( 74 FDA reports)
RASH MACULAR ( 73 FDA reports)
RETCHING ( 73 FDA reports)
SPINAL DISORDER ( 73 FDA reports)
SPINAL FRACTURE ( 73 FDA reports)
VENTRICULAR FIBRILLATION ( 73 FDA reports)
ADVERSE EVENT ( 73 FDA reports)
CAESAREAN SECTION ( 73 FDA reports)
CHOLECYSTECTOMY ( 73 FDA reports)
MIOSIS ( 73 FDA reports)
PARKINSON'S DISEASE ( 73 FDA reports)
BACK DISORDER ( 72 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 72 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 72 FDA reports)
DECREASED ACTIVITY ( 72 FDA reports)
DIFFICULTY IN WALKING ( 72 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 72 FDA reports)
INCOHERENT ( 72 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 72 FDA reports)
POOR QUALITY SLEEP ( 72 FDA reports)
PURULENCE ( 72 FDA reports)
SKIN EXFOLIATION ( 72 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 72 FDA reports)
SYNOVIAL CYST ( 72 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 71 FDA reports)
GINGIVAL DISORDER ( 71 FDA reports)
GOUT ( 71 FDA reports)
HYPERBILIRUBINAEMIA ( 71 FDA reports)
ABDOMINAL HERNIA ( 70 FDA reports)
EDENTULOUS ( 70 FDA reports)
HYPOKINESIA ( 70 FDA reports)
INTENTIONAL MISUSE ( 70 FDA reports)
POLYURIA ( 70 FDA reports)
STOMACH DISCOMFORT ( 70 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 70 FDA reports)
UPPER LIMB FRACTURE ( 70 FDA reports)
PULMONARY GRANULOMA ( 69 FDA reports)
RHINITIS ALLERGIC ( 69 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 69 FDA reports)
WOUND ( 69 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 69 FDA reports)
BONE DENSITY DECREASED ( 69 FDA reports)
BRADYKINESIA ( 69 FDA reports)
ADVERSE DRUG REACTION ( 68 FDA reports)
BILIARY DYSKINESIA ( 68 FDA reports)
BRONCHOSPASM ( 68 FDA reports)
CARDIOVASCULAR DISORDER ( 68 FDA reports)
CARPAL TUNNEL SYNDROME ( 68 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 68 FDA reports)
FAECES DISCOLOURED ( 68 FDA reports)
GINGIVAL BLEEDING ( 68 FDA reports)
LIP SWELLING ( 68 FDA reports)
MYELODYSPLASTIC SYNDROME ( 68 FDA reports)
ORAL CAVITY FISTULA ( 68 FDA reports)
ORAL INTAKE REDUCED ( 68 FDA reports)
PHOTOPHOBIA ( 68 FDA reports)
POLYNEUROPATHY ( 68 FDA reports)
RADICULOPATHY ( 68 FDA reports)
SINUS CONGESTION ( 68 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 68 FDA reports)
ABDOMINAL PAIN LOWER ( 67 FDA reports)
ACTINOMYCOSIS ( 67 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 67 FDA reports)
BODY TEMPERATURE DECREASED ( 67 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 67 FDA reports)
HERNIA ( 67 FDA reports)
LIPASE INCREASED ( 67 FDA reports)
LUNG INFECTION ( 67 FDA reports)
PARALYSIS ( 67 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 66 FDA reports)
BLOOD MAGNESIUM DECREASED ( 66 FDA reports)
CATARACT OPERATION ( 66 FDA reports)
CULTURE URINE POSITIVE ( 66 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 66 FDA reports)
GINGIVITIS ( 66 FDA reports)
HYPERTHERMIA ( 66 FDA reports)
VENTRICULAR HYPERTROPHY ( 66 FDA reports)
BACK INJURY ( 65 FDA reports)
BEDRIDDEN ( 65 FDA reports)
BLINDNESS UNILATERAL ( 65 FDA reports)
BLOOD CALCIUM INCREASED ( 65 FDA reports)
COLITIS ISCHAEMIC ( 65 FDA reports)
EXCORIATION ( 65 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 65 FDA reports)
HYPERAESTHESIA ( 65 FDA reports)
LEFT ATRIAL DILATATION ( 65 FDA reports)
LOWER LIMB FRACTURE ( 65 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 65 FDA reports)
NON-CARDIAC CHEST PAIN ( 65 FDA reports)
ODYNOPHAGIA ( 65 FDA reports)
OEDEMA MOUTH ( 65 FDA reports)
ADRENAL INSUFFICIENCY ( 64 FDA reports)
ALCOHOLISM ( 64 FDA reports)
BRUXISM ( 64 FDA reports)
COSTOCHONDRITIS ( 64 FDA reports)
CYTOLYTIC HEPATITIS ( 64 FDA reports)
DRUG SCREEN POSITIVE ( 64 FDA reports)
EXTRASYSTOLES ( 64 FDA reports)
FACET JOINT SYNDROME ( 64 FDA reports)
FEELING COLD ( 64 FDA reports)
HYPOPHOSPHATAEMIA ( 64 FDA reports)
INJECTION SITE HAEMATOMA ( 64 FDA reports)
OCULAR HYPERAEMIA ( 64 FDA reports)
PROSTATE CANCER ( 64 FDA reports)
SLUGGISHNESS ( 64 FDA reports)
URINE OUTPUT DECREASED ( 64 FDA reports)
WOUND DRAINAGE ( 64 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 63 FDA reports)
ANXIETY DISORDER ( 63 FDA reports)
BREATH ODOUR ( 63 FDA reports)
ORAL DISCOMFORT ( 63 FDA reports)
ABSCESS JAW ( 62 FDA reports)
BRAIN OEDEMA ( 62 FDA reports)
BREAST CANCER RECURRENT ( 62 FDA reports)
ENTEROCOCCAL INFECTION ( 62 FDA reports)
EOSINOPHIL COUNT INCREASED ( 62 FDA reports)
EOSINOPHILIA ( 62 FDA reports)
FEELING OF DESPAIR ( 62 FDA reports)
IMPULSIVE BEHAVIOUR ( 62 FDA reports)
ORAL DISORDER ( 62 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 62 FDA reports)
PRESCRIBED OVERDOSE ( 62 FDA reports)
SEBORRHOEIC KERATOSIS ( 62 FDA reports)
SENSORY LOSS ( 62 FDA reports)
SEQUESTRECTOMY ( 62 FDA reports)
TENDON DISORDER ( 62 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 61 FDA reports)
ACCIDENTAL EXPOSURE ( 61 FDA reports)
CONJUNCTIVITIS ( 61 FDA reports)
EUPHORIC MOOD ( 61 FDA reports)
FACIAL BONES FRACTURE ( 61 FDA reports)
ILEUS PARALYTIC ( 61 FDA reports)
LARYNGITIS ( 61 FDA reports)
MUTISM ( 61 FDA reports)
ATRIAL SEPTAL DEFECT ( 60 FDA reports)
HEARING IMPAIRED ( 60 FDA reports)
HERPES SIMPLEX ( 60 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 60 FDA reports)
POLYP ( 59 FDA reports)
SUICIDAL BEHAVIOUR ( 59 FDA reports)
THYROID NEOPLASM ( 59 FDA reports)
TORSADE DE POINTES ( 59 FDA reports)
ACUTE CORONARY SYNDROME ( 59 FDA reports)
BLOOD CULTURE POSITIVE ( 59 FDA reports)
COGWHEEL RIGIDITY ( 59 FDA reports)
CORONARY ARTERY STENOSIS ( 59 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 59 FDA reports)
ECCHYMOSIS ( 59 FDA reports)
EYE DISORDER ( 59 FDA reports)
HALLUCINATIONS, MIXED ( 59 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 59 FDA reports)
IMPAIRED WORK ABILITY ( 59 FDA reports)
LYMPHOPENIA ( 59 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 58 FDA reports)
BONE DEBRIDEMENT ( 58 FDA reports)
CEREBRAL ISCHAEMIA ( 58 FDA reports)
FAECALOMA ( 58 FDA reports)
GLOSSODYNIA ( 58 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 58 FDA reports)
MYOSITIS ( 58 FDA reports)
PURPURA ( 58 FDA reports)
SEXUAL DYSFUNCTION ( 58 FDA reports)
STUPOR ( 58 FDA reports)
VENTRICULAR HYPOKINESIA ( 57 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 57 FDA reports)
EYE SWELLING ( 57 FDA reports)
GASTROENTERITIS VIRAL ( 57 FDA reports)
HUMERUS FRACTURE ( 57 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 57 FDA reports)
ACUTE SINUSITIS ( 56 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 56 FDA reports)
DEPENDENCE ( 56 FDA reports)
JOINT SPRAIN ( 56 FDA reports)
OSTEORADIONECROSIS ( 56 FDA reports)
PANIC REACTION ( 56 FDA reports)
PHARYNGEAL OEDEMA ( 56 FDA reports)
PREMATURE BABY ( 56 FDA reports)
PROTEINURIA ( 56 FDA reports)
STEM CELL TRANSPLANT ( 56 FDA reports)
RENAL INJURY ( 55 FDA reports)
VARICOSE VEIN ( 55 FDA reports)
ACCIDENT ( 55 FDA reports)
AFFECT LABILITY ( 55 FDA reports)
BONE EROSION ( 55 FDA reports)
COLLAPSE OF LUNG ( 55 FDA reports)
ENDOCARDITIS ( 55 FDA reports)
ERUCTATION ( 55 FDA reports)
ESSENTIAL HYPERTENSION ( 55 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 55 FDA reports)
HYPERREFLEXIA ( 55 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 54 FDA reports)
CARDIOGENIC SHOCK ( 54 FDA reports)
CHOKING ( 54 FDA reports)
DENTAL FISTULA ( 54 FDA reports)
DERMATITIS CONTACT ( 54 FDA reports)
EAR DISORDER ( 54 FDA reports)
PANIC DISORDER ( 54 FDA reports)
PERSONALITY CHANGE ( 54 FDA reports)
THYROID DISORDER ( 54 FDA reports)
PERITONITIS ( 53 FDA reports)
BONE LOSS ( 53 FDA reports)
CARDIAC VALVE DISEASE ( 53 FDA reports)
DISSOCIATION ( 53 FDA reports)
ENTEROCOLITIS ( 53 FDA reports)
EYELID OEDEMA ( 53 FDA reports)
LYMPHOMA ( 53 FDA reports)
ANEURYSM ( 52 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 52 FDA reports)
CHOLANGITIS ( 52 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 52 FDA reports)
DIABETIC COMA ( 52 FDA reports)
FISTULA DISCHARGE ( 52 FDA reports)
HEPATITIS ACUTE ( 52 FDA reports)
INJECTION SITE REACTION ( 52 FDA reports)
OCCULT BLOOD POSITIVE ( 52 FDA reports)
OVARIAN CYST ( 52 FDA reports)
PLEURITIC PAIN ( 52 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 52 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 52 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 52 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 52 FDA reports)
THROAT TIGHTNESS ( 52 FDA reports)
TRACHEOBRONCHITIS ( 52 FDA reports)
TROPONIN INCREASED ( 52 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 51 FDA reports)
PSEUDOMONAS INFECTION ( 51 FDA reports)
STRESS FRACTURE ( 51 FDA reports)
SUBCUTANEOUS ABSCESS ( 51 FDA reports)
UROSEPSIS ( 51 FDA reports)
APHTHOUS STOMATITIS ( 51 FDA reports)
BLADDER DISORDER ( 51 FDA reports)
BREAST CANCER METASTATIC ( 51 FDA reports)
GOITRE ( 51 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 51 FDA reports)
MENISCUS LESION ( 51 FDA reports)
NEUROGENIC BLADDER ( 51 FDA reports)
ANGIOEDEMA ( 50 FDA reports)
ANKLE FRACTURE ( 50 FDA reports)
BLOOD CHLORIDE DECREASED ( 50 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 50 FDA reports)
HEPATIC NECROSIS ( 50 FDA reports)
HYPERTHYROIDISM ( 50 FDA reports)
HYPERTONIA ( 50 FDA reports)
HYPOACUSIS ( 50 FDA reports)
LIFE EXPECTANCY SHORTENED ( 50 FDA reports)
NYSTAGMUS ( 50 FDA reports)
PANCREATITIS CHRONIC ( 50 FDA reports)
PROCEDURAL PAIN ( 50 FDA reports)
PSYCHOMOTOR RETARDATION ( 50 FDA reports)
RALES ( 50 FDA reports)
SICK SINUS SYNDROME ( 50 FDA reports)
VASCULITIS ( 50 FDA reports)
POLYDIPSIA ( 49 FDA reports)
RASH PAPULAR ( 49 FDA reports)
SKIN CANCER ( 49 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 49 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 49 FDA reports)
LABORATORY TEST ABNORMAL ( 49 FDA reports)
LIMB DISCOMFORT ( 49 FDA reports)
ABORTION SPONTANEOUS ( 48 FDA reports)
ACUTE HEPATIC FAILURE ( 48 FDA reports)
BREAST PAIN ( 48 FDA reports)
DILATATION VENTRICULAR ( 48 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 48 FDA reports)
HOSTILITY ( 48 FDA reports)
MYOPATHY ( 48 FDA reports)
NEOPLASM ( 48 FDA reports)
NODULE ( 48 FDA reports)
TENSION ( 48 FDA reports)
THERAPY NON-RESPONDER ( 48 FDA reports)
PERSONALITY DISORDER ( 47 FDA reports)
PROCEDURAL COMPLICATION ( 47 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 47 FDA reports)
VENOUS THROMBOSIS ( 47 FDA reports)
ANURIA ( 47 FDA reports)
COLON CANCER ( 47 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 47 FDA reports)
ESCHERICHIA INFECTION ( 47 FDA reports)
FRACTURE ( 47 FDA reports)
LOCALISED INFECTION ( 47 FDA reports)
MENSTRUAL DISORDER ( 47 FDA reports)
MUSCLE TIGHTNESS ( 47 FDA reports)
NEUROPATHY ( 47 FDA reports)
ACUTE PULMONARY OEDEMA ( 46 FDA reports)
AORTIC VALVE SCLEROSIS ( 46 FDA reports)
APHAGIA ( 46 FDA reports)
CYSTITIS HAEMORRHAGIC ( 46 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 46 FDA reports)
PULSE ABSENT ( 46 FDA reports)
SKIN BURNING SENSATION ( 46 FDA reports)
SOFT TISSUE DISORDER ( 46 FDA reports)
TRISMUS ( 46 FDA reports)
WALKING AID USER ( 46 FDA reports)
WHEELCHAIR USER ( 46 FDA reports)
PAROSMIA ( 45 FDA reports)
PORTAL HYPERTENSION ( 45 FDA reports)
PROSTATE CANCER METASTATIC ( 45 FDA reports)
PYELONEPHRITIS ( 45 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 45 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 45 FDA reports)
DENTAL OPERATION ( 45 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 45 FDA reports)
GRAFT VERSUS HOST DISEASE ( 45 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 45 FDA reports)
LUNG CONSOLIDATION ( 45 FDA reports)
AMMONIA INCREASED ( 44 FDA reports)
ANGIOPATHY ( 44 FDA reports)
APLASTIC ANAEMIA ( 44 FDA reports)
ATRIOVENTRICULAR BLOCK ( 44 FDA reports)
BLOOD PROLACTIN INCREASED ( 44 FDA reports)
BONE OPERATION ( 44 FDA reports)
BREAST MASS ( 44 FDA reports)
DEPRESSIVE SYMPTOM ( 44 FDA reports)
DRUG ERUPTION ( 44 FDA reports)
ENTERITIS ( 44 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 44 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 44 FDA reports)
MOTOR DYSFUNCTION ( 44 FDA reports)
MUSCLE STRAIN ( 44 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 44 FDA reports)
PROSTATOMEGALY ( 44 FDA reports)
SPINAL CORD COMPRESSION ( 44 FDA reports)
TENDON RUPTURE ( 44 FDA reports)
URINARY HESITATION ( 44 FDA reports)
PATHOLOGICAL GAMBLING ( 43 FDA reports)
PELVIC FRACTURE ( 43 FDA reports)
PREMATURE LABOUR ( 43 FDA reports)
REFLUX OESOPHAGITIS ( 43 FDA reports)
TACHYARRHYTHMIA ( 43 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 43 FDA reports)
AORTIC CALCIFICATION ( 43 FDA reports)
CHEILITIS ( 43 FDA reports)
DUODENITIS ( 43 FDA reports)
ERYTHEMA MULTIFORME ( 43 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 43 FDA reports)
FOOT DEFORMITY ( 43 FDA reports)
H1N1 INFLUENZA ( 43 FDA reports)
HIP ARTHROPLASTY ( 43 FDA reports)
INGROWING NAIL ( 43 FDA reports)
KLEBSIELLA INFECTION ( 43 FDA reports)
LUMBAR RADICULOPATHY ( 43 FDA reports)
NECROSIS ( 43 FDA reports)
NO ADVERSE EVENT ( 43 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 42 FDA reports)
CYSTOCELE ( 42 FDA reports)
DENTURE WEARER ( 42 FDA reports)
DIASTOLIC DYSFUNCTION ( 42 FDA reports)
DRUG LEVEL DECREASED ( 42 FDA reports)
DYSTHYMIC DISORDER ( 42 FDA reports)
GASTRIC PH DECREASED ( 42 FDA reports)
HYPERPARATHYROIDISM ( 42 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 42 FDA reports)
JOINT DISLOCATION ( 42 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 42 FDA reports)
PROSTATITIS ( 42 FDA reports)
VIITH NERVE PARALYSIS ( 42 FDA reports)
PEPTIC ULCER ( 41 FDA reports)
TIBIA FRACTURE ( 41 FDA reports)
VITAMIN B12 DEFICIENCY ( 41 FDA reports)
ADHESION ( 41 FDA reports)
ALCOHOL POISONING ( 41 FDA reports)
DEMYELINATION ( 41 FDA reports)
DEREALISATION ( 41 FDA reports)
EMBOLISM ( 41 FDA reports)
EYE IRRITATION ( 41 FDA reports)
FEELING DRUNK ( 41 FDA reports)
HAEMODYNAMIC INSTABILITY ( 41 FDA reports)
HEPATIC ENCEPHALOPATHY ( 41 FDA reports)
HYPERKERATOSIS ( 41 FDA reports)
IMMUNOSUPPRESSION ( 41 FDA reports)
METASTASIS ( 41 FDA reports)
MUSCLE ATROPHY ( 41 FDA reports)
NECK MASS ( 41 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 41 FDA reports)
ABSCESS DRAINAGE ( 40 FDA reports)
AKINESIA ( 40 FDA reports)
BREATH SOUNDS ABNORMAL ( 40 FDA reports)
CHOLECYSTITIS ACUTE ( 40 FDA reports)
DEPERSONALISATION ( 40 FDA reports)
DIABETIC RETINOPATHY ( 40 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 40 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 40 FDA reports)
ENURESIS ( 40 FDA reports)
FACIAL PALSY ( 40 FDA reports)
HYDROCELE ( 40 FDA reports)
HYPOMANIA ( 40 FDA reports)
INADEQUATE ANALGESIA ( 40 FDA reports)
JAUNDICE CHOLESTATIC ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 40 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 40 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 40 FDA reports)
MEDICATION RESIDUE ( 40 FDA reports)
MITRAL VALVE CALCIFICATION ( 40 FDA reports)
MUSCLE CRAMP ( 40 FDA reports)
PROTEIN TOTAL DECREASED ( 40 FDA reports)
SENSATION OF HEAVINESS ( 40 FDA reports)
PHLEBITIS ( 39 FDA reports)
RESPIRATORY ACIDOSIS ( 39 FDA reports)
SKELETAL INJURY ( 39 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 39 FDA reports)
VAGINAL INFECTION ( 39 FDA reports)
ANGIONEUROTIC OEDEMA ( 39 FDA reports)
ASPHYXIA ( 39 FDA reports)
BLOOD AMYLASE INCREASED ( 39 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 39 FDA reports)
BONE SWELLING ( 39 FDA reports)
DERMATITIS EXFOLIATIVE ( 39 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 39 FDA reports)
DRUG PRESCRIBING ERROR ( 39 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 39 FDA reports)
FOOD CRAVING ( 39 FDA reports)
GINGIVAL ERYTHEMA ( 39 FDA reports)
LARYNGOSPASM ( 39 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 39 FDA reports)
METABOLIC ENCEPHALOPATHY ( 39 FDA reports)
MITRAL VALVE PROLAPSE ( 39 FDA reports)
MORBID THOUGHTS ( 39 FDA reports)
NECK INJURY ( 39 FDA reports)
ABORTION INDUCED ( 38 FDA reports)
ACUTE PRERENAL FAILURE ( 38 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 38 FDA reports)
BLOOD BICARBONATE DECREASED ( 38 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 38 FDA reports)
BONE FRAGMENTATION ( 38 FDA reports)
COLON ADENOMA ( 38 FDA reports)
COMMUNICATION DISORDER ( 38 FDA reports)
DRUG TOLERANCE ( 38 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 38 FDA reports)
FLUID INTAKE REDUCED ( 38 FDA reports)
GANGRENE ( 38 FDA reports)
GASTROINTESTINAL PAIN ( 38 FDA reports)
HYPERPHAGIA ( 38 FDA reports)
HYPERTENSIVE CRISIS ( 38 FDA reports)
HYPERTENSIVE HEART DISEASE ( 38 FDA reports)
INITIAL INSOMNIA ( 38 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 38 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 38 FDA reports)
TOXIC SKIN ERUPTION ( 38 FDA reports)
WRONG DRUG ADMINISTERED ( 38 FDA reports)
PHOTOSENSITIVITY REACTION ( 37 FDA reports)
SCREAMING ( 37 FDA reports)
SELF ESTEEM DECREASED ( 37 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 37 FDA reports)
THYROID CANCER ( 37 FDA reports)
WOUND INFECTION ( 37 FDA reports)
AORTIC STENOSIS ( 37 FDA reports)
BLOOD PH DECREASED ( 37 FDA reports)
CARDIAC PACEMAKER INSERTION ( 37 FDA reports)
CHEST X-RAY ABNORMAL ( 37 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 37 FDA reports)
HAEMOTHORAX ( 37 FDA reports)
HEPATITIS CHOLESTATIC ( 37 FDA reports)
HYSTERECTOMY ( 37 FDA reports)
MASTOIDITIS ( 37 FDA reports)
MENORRHAGIA ( 37 FDA reports)
MOUTH HAEMORRHAGE ( 37 FDA reports)
NAIL DISORDER ( 37 FDA reports)
NEPHROPATHY ( 37 FDA reports)
ACNE ( 36 FDA reports)
ACUTE PSYCHOSIS ( 36 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 36 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 36 FDA reports)
BLOOD COUNT ABNORMAL ( 36 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 36 FDA reports)
BREAST CANCER FEMALE ( 36 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 36 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 36 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 36 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 36 FDA reports)
GRANULOMA ( 36 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 36 FDA reports)
HODGKIN'S DISEASE ( 36 FDA reports)
HYPERPROLACTINAEMIA ( 36 FDA reports)
HYPERTONIC BLADDER ( 36 FDA reports)
INAPPROPRIATE AFFECT ( 36 FDA reports)
ISCHAEMIC STROKE ( 36 FDA reports)
LIVER INJURY ( 36 FDA reports)
LOSS OF LIBIDO ( 36 FDA reports)
MYOCARDITIS ( 36 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 36 FDA reports)
OESOPHAGEAL DISORDER ( 36 FDA reports)
OSTEOCHONDROSIS ( 36 FDA reports)
PLANTAR FASCIITIS ( 36 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 36 FDA reports)
POSTURE ABNORMAL ( 36 FDA reports)
RESPIRATORY RATE DECREASED ( 36 FDA reports)
SINUS HEADACHE ( 36 FDA reports)
TOBACCO USER ( 36 FDA reports)
UTERINE HAEMORRHAGE ( 36 FDA reports)
UTERINE LEIOMYOMA ( 36 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 36 FDA reports)
SOCIAL PROBLEM ( 35 FDA reports)
STREPTOCOCCAL INFECTION ( 35 FDA reports)
TUMOUR LYSIS SYNDROME ( 35 FDA reports)
BLOOD CREATINE INCREASED ( 35 FDA reports)
BLOOD PRESSURE ABNORMAL ( 35 FDA reports)
BONE MARROW TRANSPLANT ( 35 FDA reports)
CACHEXIA ( 35 FDA reports)
CATHETERISATION CARDIAC ( 35 FDA reports)
COLITIS ULCERATIVE ( 35 FDA reports)
DERMATITIS ALLERGIC ( 35 FDA reports)
DRY THROAT ( 35 FDA reports)
DYSGRAPHIA ( 35 FDA reports)
EAR CONGESTION ( 35 FDA reports)
ENDOTRACHEAL INTUBATION ( 35 FDA reports)
EYE PRURITUS ( 35 FDA reports)
EYELID DISORDER ( 35 FDA reports)
FLAT AFFECT ( 35 FDA reports)
HERNIA REPAIR ( 35 FDA reports)
HICCUPS ( 35 FDA reports)
METABOLIC DISORDER ( 35 FDA reports)
ORTHOPNOEA ( 35 FDA reports)
OVARIAN CANCER ( 35 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 34 FDA reports)
BARRETT'S OESOPHAGUS ( 34 FDA reports)
CARDIAC FAILURE ACUTE ( 34 FDA reports)
DIZZINESS POSTURAL ( 34 FDA reports)
DRUG SCREEN NEGATIVE ( 34 FDA reports)
EYELID PTOSIS ( 34 FDA reports)
FIBROSIS ( 34 FDA reports)
HEPATOSPLENOMEGALY ( 34 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 34 FDA reports)
KETOACIDOSIS ( 34 FDA reports)
KIDNEY INFECTION ( 34 FDA reports)
MELANOCYTIC NAEVUS ( 34 FDA reports)
METASTASES TO THORAX ( 34 FDA reports)
NERVE INJURY ( 34 FDA reports)
NEUROTOXICITY ( 34 FDA reports)
PANCREATIC CYST ( 34 FDA reports)
PERICARDITIS ( 34 FDA reports)
PROTEIN URINE PRESENT ( 34 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 34 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 34 FDA reports)
SPUTUM CULTURE POSITIVE ( 34 FDA reports)
TEARFULNESS ( 34 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 34 FDA reports)
PARONYCHIA ( 33 FDA reports)
RENAL PAIN ( 33 FDA reports)
SENSATION OF FOREIGN BODY ( 33 FDA reports)
TOXIC ENCEPHALOPATHY ( 33 FDA reports)
APPLICATION SITE ERYTHEMA ( 33 FDA reports)
BONE NEOPLASM MALIGNANT ( 33 FDA reports)
BRAIN NEOPLASM ( 33 FDA reports)
CARDIAC ENZYMES INCREASED ( 33 FDA reports)
CERVICOBRACHIAL SYNDROME ( 33 FDA reports)
DEAFNESS NEUROSENSORY ( 33 FDA reports)
DILATATION ATRIAL ( 33 FDA reports)
FAMILY STRESS ( 33 FDA reports)
FRUSTRATION ( 33 FDA reports)
GASTRITIS EROSIVE ( 33 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 33 FDA reports)
HOMICIDAL IDEATION ( 33 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 33 FDA reports)
LACUNAR INFARCTION ( 33 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 33 FDA reports)
MICROCYTIC ANAEMIA ( 33 FDA reports)
OLIGURIA ( 33 FDA reports)
ABDOMINAL ABSCESS ( 32 FDA reports)
AREFLEXIA ( 32 FDA reports)
BILIARY DILATATION ( 32 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 32 FDA reports)
BLOOD SODIUM INCREASED ( 32 FDA reports)
BODY HEIGHT DECREASED ( 32 FDA reports)
BRAIN HERNIATION ( 32 FDA reports)
DEVICE MALFUNCTION ( 32 FDA reports)
DIABETIC COMPLICATION ( 32 FDA reports)
FEELING GUILTY ( 32 FDA reports)
GASTRIC HAEMORRHAGE ( 32 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 32 FDA reports)
GINGIVAL OEDEMA ( 32 FDA reports)
INJURY ASPHYXIATION ( 32 FDA reports)
MALIGNANT MELANOMA ( 32 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 32 FDA reports)
NASAL SEPTUM DEVIATION ( 32 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 32 FDA reports)
ORAL HERPES ( 32 FDA reports)
PERIODONTITIS ( 32 FDA reports)
SELF-INJURIOUS IDEATION ( 32 FDA reports)
SERRATIA INFECTION ( 32 FDA reports)
VENTRICULAR ARRHYTHMIA ( 32 FDA reports)
VISUAL FIELD DEFECT ( 32 FDA reports)
PNEUMONIA BACTERIAL ( 31 FDA reports)
SENSITIVITY OF TEETH ( 31 FDA reports)
THORACOTOMY ( 31 FDA reports)
TOBACCO ABUSE ( 31 FDA reports)
TRANSFUSION ( 31 FDA reports)
TUBERCULOSIS ( 31 FDA reports)
URINE FLOW DECREASED ( 31 FDA reports)
ABNORMAL SENSATION IN EYE ( 31 FDA reports)
AUTOIMMUNE DISORDER ( 31 FDA reports)
BIPOLAR I DISORDER ( 31 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 31 FDA reports)
FEEDING DISORDER ( 31 FDA reports)
HEMIPLEGIA ( 31 FDA reports)
HEPATIC CONGESTION ( 31 FDA reports)
HOMICIDE ( 31 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 31 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 31 FDA reports)
KNEE ARTHROPLASTY ( 31 FDA reports)
OVERWEIGHT ( 31 FDA reports)
ABDOMINAL MASS ( 30 FDA reports)
APPENDICITIS ( 30 FDA reports)
ATROPHY ( 30 FDA reports)
BLOOD CREATININE DECREASED ( 30 FDA reports)
BREAST CALCIFICATIONS ( 30 FDA reports)
CAECITIS ( 30 FDA reports)
CERUMEN IMPACTION ( 30 FDA reports)
DUODENAL ULCER ( 30 FDA reports)
ESCHERICHIA BACTERAEMIA ( 30 FDA reports)
GINGIVAL EROSION ( 30 FDA reports)
HEPATORENAL SYNDROME ( 30 FDA reports)
HILAR LYMPHADENOPATHY ( 30 FDA reports)
INTRAOCULAR LENS IMPLANT ( 30 FDA reports)
MENSTRUATION IRREGULAR ( 30 FDA reports)
MULTIPLE FRACTURES ( 30 FDA reports)
NEUROLOGICAL SYMPTOM ( 30 FDA reports)
OESOPHAGEAL STENOSIS ( 30 FDA reports)
PERIPHERAL ISCHAEMIA ( 30 FDA reports)
PLASMACYTOMA ( 30 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 30 FDA reports)
RECTOCELE ( 30 FDA reports)
RHONCHI ( 30 FDA reports)
SPLEEN DISORDER ( 30 FDA reports)
SPUTUM DISCOLOURED ( 30 FDA reports)
STRESS URINARY INCONTINENCE ( 30 FDA reports)
TACHYPHRENIA ( 30 FDA reports)
TESTICULAR PAIN ( 30 FDA reports)
VENTRICULAR DYSFUNCTION ( 30 FDA reports)
VITAMIN D DECREASED ( 30 FDA reports)
WRIST FRACTURE ( 30 FDA reports)
PCO2 DECREASED ( 29 FDA reports)
PERSECUTORY DELUSION ( 29 FDA reports)
POOR PERIPHERAL CIRCULATION ( 29 FDA reports)
PROCTALGIA ( 29 FDA reports)
PRODUCT ADHESION ISSUE ( 29 FDA reports)
RENAL ATROPHY ( 29 FDA reports)
SACROILIITIS ( 29 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 29 FDA reports)
STENT PLACEMENT ( 29 FDA reports)
TENDON INJURY ( 29 FDA reports)
TONGUE BITING ( 29 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 29 FDA reports)
ANAPHYLACTIC SHOCK ( 29 FDA reports)
BACTERIAL SEPSIS ( 29 FDA reports)
BILE DUCT STENOSIS ( 29 FDA reports)
CEREBELLAR INFARCTION ( 29 FDA reports)
CEREBROVASCULAR DISORDER ( 29 FDA reports)
CONCUSSION ( 29 FDA reports)
DERMATITIS BULLOUS ( 29 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 29 FDA reports)
FORMICATION ( 29 FDA reports)
GINGIVAL ULCERATION ( 29 FDA reports)
GUN SHOT WOUND ( 29 FDA reports)
HAEMOLYSIS ( 29 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 29 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 29 FDA reports)
HEPATIC NEOPLASM ( 29 FDA reports)
HEPATOCELLULAR DAMAGE ( 29 FDA reports)
HYPOAESTHESIA FACIAL ( 29 FDA reports)
HYPOVENTILATION ( 29 FDA reports)
INCREASED TENDENCY TO BRUISE ( 29 FDA reports)
INTENTION TREMOR ( 29 FDA reports)
ISCHAEMIC HEPATITIS ( 29 FDA reports)
LEG AMPUTATION ( 29 FDA reports)
LOSS OF EMPLOYMENT ( 29 FDA reports)
MALLORY-WEISS SYNDROME ( 29 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 29 FDA reports)
NON-SMALL CELL LUNG CANCER ( 29 FDA reports)
OTITIS MEDIA ACUTE ( 29 FDA reports)
ABDOMINAL TENDERNESS ( 28 FDA reports)
ADJUSTMENT DISORDER ( 28 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 28 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 28 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 28 FDA reports)
BRAIN INJURY ( 28 FDA reports)
BREAST CYST ( 28 FDA reports)
CERVICAL SPINAL STENOSIS ( 28 FDA reports)
DERMATITIS ACNEIFORM ( 28 FDA reports)
DEVELOPMENTAL DELAY ( 28 FDA reports)
DIET REFUSAL ( 28 FDA reports)
DYSPHORIA ( 28 FDA reports)
EMPYEMA ( 28 FDA reports)
ENCEPHALITIS ( 28 FDA reports)
EYE MOVEMENT DISORDER ( 28 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 28 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 28 FDA reports)
GRIP STRENGTH DECREASED ( 28 FDA reports)
HYPERLACTACIDAEMIA ( 28 FDA reports)
HYPOCHLORAEMIA ( 28 FDA reports)
LOGORRHOEA ( 28 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 28 FDA reports)
MARROW HYPERPLASIA ( 28 FDA reports)
MENINGITIS ASEPTIC ( 28 FDA reports)
MUSCULOSKELETAL DISORDER ( 28 FDA reports)
NEPHROTIC SYNDROME ( 28 FDA reports)
ORAL SURGERY ( 28 FDA reports)
PLASMACYTOSIS ( 28 FDA reports)
PLEUROTHOTONUS ( 28 FDA reports)
PRESBYOPIA ( 28 FDA reports)
PULMONARY HAEMORRHAGE ( 28 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 28 FDA reports)
REPETITIVE SPEECH ( 28 FDA reports)
SNORING ( 28 FDA reports)
SOMNAMBULISM ( 28 FDA reports)
SUBILEUS ( 28 FDA reports)
THROMBOCYTOSIS ( 28 FDA reports)
TOOTH REPAIR ( 28 FDA reports)
VITAMIN D DEFICIENCY ( 28 FDA reports)
PERFORMANCE STATUS DECREASED ( 27 FDA reports)
PULMONARY MASS ( 27 FDA reports)
RADICULAR PAIN ( 27 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 27 FDA reports)
SEASONAL ALLERGY ( 27 FDA reports)
SEPSIS SYNDROME ( 27 FDA reports)
SERUM FERRITIN INCREASED ( 27 FDA reports)
TENOSYNOVITIS ( 27 FDA reports)
THROMBOSIS IN DEVICE ( 27 FDA reports)
VAGINAL DISCHARGE ( 27 FDA reports)
VOCAL CORD PARALYSIS ( 27 FDA reports)
ACTINIC KERATOSIS ( 27 FDA reports)
ACUTE ABDOMEN ( 27 FDA reports)
AUTOIMMUNE HEPATITIS ( 27 FDA reports)
COLECTOMY ( 27 FDA reports)
COR PULMONALE ( 27 FDA reports)
DEVICE FAILURE ( 27 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 27 FDA reports)
FACIAL PARESIS ( 27 FDA reports)
FIBRIN D DIMER INCREASED ( 27 FDA reports)
GASTROINTESTINAL INFECTION ( 27 FDA reports)
HAEMORRHAGIC DIATHESIS ( 27 FDA reports)
HEPATITIS TOXIC ( 27 FDA reports)
HYPERCAPNIA ( 27 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 27 FDA reports)
LIPOMA ( 27 FDA reports)
MACROCYTOSIS ( 27 FDA reports)
MUSCLE SPASTICITY ( 27 FDA reports)
NERVE COMPRESSION ( 27 FDA reports)
ACCIDENTAL DEATH ( 26 FDA reports)
APPENDICITIS PERFORATED ( 26 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 26 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 26 FDA reports)
BREAST TENDERNESS ( 26 FDA reports)
CALCULUS BLADDER ( 26 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 26 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 26 FDA reports)
DIABETIC FOOT ( 26 FDA reports)
DYSAESTHESIA ( 26 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 26 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 26 FDA reports)
IMMOBILE ( 26 FDA reports)
INFECTED SKIN ULCER ( 26 FDA reports)
INJECTION SITE PRURITUS ( 26 FDA reports)
INTESTINAL ISCHAEMIA ( 26 FDA reports)
INTRACRANIAL ANEURYSM ( 26 FDA reports)
LEFT VENTRICULAR FAILURE ( 26 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 26 FDA reports)
LIGAMENT SPRAIN ( 26 FDA reports)
METASTASES TO PELVIS ( 26 FDA reports)
METRORRHAGIA ( 26 FDA reports)
MUSCLE INJURY ( 26 FDA reports)
OBSTRUCTIVE UROPATHY ( 26 FDA reports)
ORAL DISCHARGE ( 26 FDA reports)
RASH PUSTULAR ( 26 FDA reports)
RIGHT ATRIAL DILATATION ( 26 FDA reports)
SINUS OPERATION ( 26 FDA reports)
THROMBOPHLEBITIS ( 26 FDA reports)
TOOTH IMPACTED ( 26 FDA reports)
TROPONIN I INCREASED ( 26 FDA reports)
UMBILICAL HERNIA ( 26 FDA reports)
URINE COLOUR ABNORMAL ( 26 FDA reports)
VITREOUS FLOATERS ( 26 FDA reports)
WEIGHT FLUCTUATION ( 26 FDA reports)
POLYMYALGIA RHEUMATICA ( 25 FDA reports)
QUADRIPARESIS ( 25 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 25 FDA reports)
SARCOIDOSIS ( 25 FDA reports)
SEBORRHOEIC DERMATITIS ( 25 FDA reports)
SPONDYLOLYSIS ( 25 FDA reports)
SUDDEN CARDIAC DEATH ( 25 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 25 FDA reports)
VASCULAR CALCIFICATION ( 25 FDA reports)
AGORAPHOBIA ( 25 FDA reports)
APPLICATION SITE PRURITUS ( 25 FDA reports)
ASPIRATION PLEURAL CAVITY ( 25 FDA reports)
BLEPHARITIS ( 25 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 25 FDA reports)
CHANGE OF BOWEL HABIT ( 25 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 25 FDA reports)
CONVERSION DISORDER ( 25 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 25 FDA reports)
DERMAL CYST ( 25 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 25 FDA reports)
EPIDIDYMITIS ( 25 FDA reports)
GALACTORRHOEA ( 25 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 25 FDA reports)
HEPATOCELLULAR INJURY ( 25 FDA reports)
HYPERAMMONAEMIA ( 25 FDA reports)
HYPOVOLAEMIC SHOCK ( 25 FDA reports)
MEDICAL DEVICE COMPLICATION ( 25 FDA reports)
MENINGIOMA ( 25 FDA reports)
MITRAL VALVE SCLEROSIS ( 25 FDA reports)
NASAL DISORDER ( 25 FDA reports)
NASAL ULCER ( 25 FDA reports)
PANCREATIC DISORDER ( 25 FDA reports)
ADENOMA BENIGN ( 24 FDA reports)
APPETITE DISORDER ( 24 FDA reports)
BEHCET'S SYNDROME ( 24 FDA reports)
BILIARY TRACT DISORDER ( 24 FDA reports)
CAROTID ARTERY OCCLUSION ( 24 FDA reports)
CONDUCTION DISORDER ( 24 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 24 FDA reports)
ENTHESOPATHY ( 24 FDA reports)
GASTRIC POLYPS ( 24 FDA reports)
GLOSSITIS ( 24 FDA reports)
HYDROCEPHALUS ( 24 FDA reports)
ILEAL ULCER ( 24 FDA reports)
IMPAIRED SELF-CARE ( 24 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 24 FDA reports)
LARYNGEAL OEDEMA ( 24 FDA reports)
MITRAL VALVE DISEASE ( 24 FDA reports)
MONOCYTE COUNT INCREASED ( 24 FDA reports)
NEONATAL DISORDER ( 24 FDA reports)
OESOPHAGEAL PAIN ( 24 FDA reports)
OESOPHAGEAL ULCER ( 24 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 24 FDA reports)
RESORPTION BONE INCREASED ( 24 FDA reports)
RIGHT VENTRICULAR FAILURE ( 24 FDA reports)
SCAB ( 24 FDA reports)
SELF-MEDICATION ( 24 FDA reports)
SKIN HAEMORRHAGE ( 24 FDA reports)
SKIN WARM ( 24 FDA reports)
SOMATOFORM DISORDER ( 24 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 24 FDA reports)
PHYSICAL ASSAULT ( 23 FDA reports)
PITTING OEDEMA ( 23 FDA reports)
PLEURISY ( 23 FDA reports)
PULMONARY THROMBOSIS ( 23 FDA reports)
SEROMA ( 23 FDA reports)
SHOULDER PAIN ( 23 FDA reports)
SUBMANDIBULAR MASS ( 23 FDA reports)
SUBSTANCE ABUSE ( 23 FDA reports)
TONGUE DISCOLOURATION ( 23 FDA reports)
VERTIGO POSITIONAL ( 23 FDA reports)
VULVOVAGINAL DRYNESS ( 23 FDA reports)
AGEUSIA ( 23 FDA reports)
BILE DUCT OBSTRUCTION ( 23 FDA reports)
BRAIN DEATH ( 23 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 23 FDA reports)
EFFUSION ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 23 FDA reports)
EPIGASTRIC DISCOMFORT ( 23 FDA reports)
FISTULA REPAIR ( 23 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 23 FDA reports)
GASTROINTESTINAL NECROSIS ( 23 FDA reports)
HAND FRACTURE ( 23 FDA reports)
HEPATIC FIBROSIS ( 23 FDA reports)
HYPERPLASIA ( 23 FDA reports)
INTERMITTENT CLAUDICATION ( 23 FDA reports)
KNEE OPERATION ( 23 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 23 FDA reports)
MUSCLE CONTRACTURE ( 23 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 23 FDA reports)
NODAL RHYTHM ( 23 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 23 FDA reports)
ACCIDENT AT WORK ( 22 FDA reports)
ALVEOLITIS ( 22 FDA reports)
ANIMAL BITE ( 22 FDA reports)
ARTERIOSPASM CORONARY ( 22 FDA reports)
ATHEROSCLEROSIS ( 22 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 22 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 22 FDA reports)
BLADDER PROLAPSE ( 22 FDA reports)
BLOOD PH INCREASED ( 22 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 22 FDA reports)
BREAKTHROUGH PAIN ( 22 FDA reports)
BRONCHIECTASIS ( 22 FDA reports)
BRONCHITIS CHRONIC ( 22 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 22 FDA reports)
CARDIAC TAMPONADE ( 22 FDA reports)
CHONDROMALACIA ( 22 FDA reports)
EYE HAEMORRHAGE ( 22 FDA reports)
FAECES PALE ( 22 FDA reports)
FLIGHT OF IDEAS ( 22 FDA reports)
FORAMEN MAGNUM STENOSIS ( 22 FDA reports)
FRACTURED SACRUM ( 22 FDA reports)
HAEMOLYTIC ANAEMIA ( 22 FDA reports)
HAEMORRHAGIC STROKE ( 22 FDA reports)
HEAD DISCOMFORT ( 22 FDA reports)
HIGH FREQUENCY ABLATION ( 22 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 22 FDA reports)
LUNG HYPERINFLATION ( 22 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 22 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 22 FDA reports)
MAMMOGRAM ABNORMAL ( 22 FDA reports)
METASTASES TO BONE MARROW ( 22 FDA reports)
MONOPLEGIA ( 22 FDA reports)
MYOPIA ( 22 FDA reports)
NEPHROPATHY TOXIC ( 22 FDA reports)
NEUTROPENIC SEPSIS ( 22 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 22 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 22 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 22 FDA reports)
PNEUMATOSIS INTESTINALIS ( 22 FDA reports)
RESUSCITATION ( 22 FDA reports)
ROSACEA ( 22 FDA reports)
SKIN FISSURES ( 22 FDA reports)
SKIN INDURATION ( 22 FDA reports)
SPONDYLOSIS ( 22 FDA reports)
TONGUE ULCERATION ( 22 FDA reports)
URINARY TRACT OBSTRUCTION ( 22 FDA reports)
VAGINAL PROLAPSE ( 22 FDA reports)
VENA CAVA FILTER INSERTION ( 22 FDA reports)
VENOOCCLUSIVE DISEASE ( 22 FDA reports)
VENOUS THROMBOSIS LIMB ( 22 FDA reports)
WOUND COMPLICATION ( 22 FDA reports)
PARTIAL SEIZURES ( 21 FDA reports)
PERIPHERAL EMBOLISM ( 21 FDA reports)
PLEURAL FIBROSIS ( 21 FDA reports)
PO2 DECREASED ( 21 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 21 FDA reports)
PROTEIN TOTAL INCREASED ( 21 FDA reports)
PUPILS UNEQUAL ( 21 FDA reports)
REFLUX GASTRITIS ( 21 FDA reports)
SKIN NEOPLASM EXCISION ( 21 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 21 FDA reports)
STARING ( 21 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 21 FDA reports)
TOE DEFORMITY ( 21 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 21 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 21 FDA reports)
AMAUROSIS FUGAX ( 21 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 21 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 21 FDA reports)
BRAIN SCAN ABNORMAL ( 21 FDA reports)
CAROTID BRUIT ( 21 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 21 FDA reports)
CLOSTRIDIUM COLITIS ( 21 FDA reports)
COELIAC DISEASE ( 21 FDA reports)
CORONARY ANGIOPLASTY ( 21 FDA reports)
DENTAL DISCOMFORT ( 21 FDA reports)
DRUG DISPENSING ERROR ( 21 FDA reports)
DRUG INTERACTION POTENTIATION ( 21 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 21 FDA reports)
DYSPHEMIA ( 21 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 21 FDA reports)
EYE OPERATION ( 21 FDA reports)
FIBROUS HISTIOCYTOMA ( 21 FDA reports)
FIBULA FRACTURE ( 21 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 21 FDA reports)
HEPATIC MASS ( 21 FDA reports)
HEPATIC PAIN ( 21 FDA reports)
INCISIONAL DRAINAGE ( 21 FDA reports)
INGUINAL HERNIA ( 21 FDA reports)
INJECTION SITE SWELLING ( 21 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 21 FDA reports)
LEUKOENCEPHALOPATHY ( 21 FDA reports)
MASTECTOMY ( 21 FDA reports)
METASTASES TO SKIN ( 21 FDA reports)
MUSCLE HAEMORRHAGE ( 21 FDA reports)
NARCOTIC INTOXICATION ( 21 FDA reports)
NEURITIS ( 21 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 21 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 21 FDA reports)
PARAPLEGIA ( 21 FDA reports)
ADRENAL DISORDER ( 20 FDA reports)
ASTIGMATISM ( 20 FDA reports)
BLOOD IRON DECREASED ( 20 FDA reports)
BLOOD OSMOLARITY INCREASED ( 20 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 20 FDA reports)
BONE SCAN ABNORMAL ( 20 FDA reports)
BRONCHITIS ACUTE ( 20 FDA reports)
BULLOUS LUNG DISEASE ( 20 FDA reports)
BUNION ( 20 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 20 FDA reports)
COMPLEX PARTIAL SEIZURES ( 20 FDA reports)
CREPITATIONS ( 20 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 20 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 20 FDA reports)
EXANTHEM ( 20 FDA reports)
FACE INJURY ( 20 FDA reports)
FOAMING AT MOUTH ( 20 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 20 FDA reports)
GASTROENTERITIS RADIATION ( 20 FDA reports)
GINGIVAL RECESSION ( 20 FDA reports)
HAEMANGIOMA ( 20 FDA reports)
HAEMATOCRIT INCREASED ( 20 FDA reports)
HAEMORRHAGIC ANAEMIA ( 20 FDA reports)
INTESTINAL POLYP ( 20 FDA reports)
KERATITIS ( 20 FDA reports)
LABYRINTHITIS ( 20 FDA reports)
LEUKAEMIA ( 20 FDA reports)
LONG QT SYNDROME ( 20 FDA reports)
LUMBAR SPINE FLATTENING ( 20 FDA reports)
LYMPHADENECTOMY ( 20 FDA reports)
MALABSORPTION ( 20 FDA reports)
MASKED FACIES ( 20 FDA reports)
METASTASES TO ADRENALS ( 20 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 20 FDA reports)
ONYCHALGIA ( 20 FDA reports)
OTITIS EXTERNA ( 20 FDA reports)
PELVIC FLUID COLLECTION ( 20 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 20 FDA reports)
PIGMENTATION DISORDER ( 20 FDA reports)
POLYCYSTIC OVARIES ( 20 FDA reports)
POSTOPERATIVE ILEUS ( 20 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 20 FDA reports)
PUPIL FIXED ( 20 FDA reports)
SKIN TIGHTNESS ( 20 FDA reports)
SMEAR CERVIX ABNORMAL ( 20 FDA reports)
SPINAL CORD DISORDER ( 20 FDA reports)
STRESS SYMPTOMS ( 20 FDA reports)
SYNCOPE VASOVAGAL ( 20 FDA reports)
URETERIC OBSTRUCTION ( 20 FDA reports)
VITAMIN B12 INCREASED ( 20 FDA reports)
PETIT MAL EPILEPSY ( 19 FDA reports)
PLATELET COUNT ABNORMAL ( 19 FDA reports)
PNEUMONIA VIRAL ( 19 FDA reports)
PROTEIN URINE ( 19 FDA reports)
QRS AXIS ABNORMAL ( 19 FDA reports)
SENSATION OF PRESSURE ( 19 FDA reports)
SKIN HYPERTROPHY ( 19 FDA reports)
SKIN REACTION ( 19 FDA reports)
STREPTOCOCCAL SEPSIS ( 19 FDA reports)
TEMPERATURE INTOLERANCE ( 19 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 19 FDA reports)
TOOTH DEPOSIT ( 19 FDA reports)
VARICOCELE ( 19 FDA reports)
VASCULAR ANOMALY ( 19 FDA reports)
WOUND DEBRIDEMENT ( 19 FDA reports)
AGITATED DEPRESSION ( 19 FDA reports)
AMENORRHOEA ( 19 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 19 FDA reports)
AXILLARY PAIN ( 19 FDA reports)
BILE DUCT STONE ( 19 FDA reports)
BLADDER CANCER ( 19 FDA reports)
BLADDER OBSTRUCTION ( 19 FDA reports)
BLEPHAROSPASM ( 19 FDA reports)
BLOOD OSMOLARITY DECREASED ( 19 FDA reports)
BODY MASS INDEX INCREASED ( 19 FDA reports)
BREAST NECROSIS ( 19 FDA reports)
BREAST OPERATION ( 19 FDA reports)
CAROTID ARTERY DISEASE ( 19 FDA reports)
CERVICAL DYSPLASIA ( 19 FDA reports)
CHOREA ( 19 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 19 FDA reports)
CLONUS ( 19 FDA reports)
COLON CANCER METASTATIC ( 19 FDA reports)
DIABETIC NEPHROPATHY ( 19 FDA reports)
DRUG EFFECT INCREASED ( 19 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 19 FDA reports)
EMBOLISM VENOUS ( 19 FDA reports)
FOREIGN BODY REACTION ( 19 FDA reports)
FRACTURE NONUNION ( 19 FDA reports)
HELICOBACTER INFECTION ( 19 FDA reports)
LIGAMENT RUPTURE ( 19 FDA reports)
MEDIASTINAL MASS ( 19 FDA reports)
MONOCLONAL GAMMOPATHY ( 19 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 19 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 19 FDA reports)
NEUTROPENIC INFECTION ( 19 FDA reports)
ABDOMINAL RIGIDITY ( 18 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 18 FDA reports)
ALVEOLAR OSTEITIS ( 18 FDA reports)
ANION GAP INCREASED ( 18 FDA reports)
ANORECTAL DISCOMFORT ( 18 FDA reports)
ANOXIC ENCEPHALOPATHY ( 18 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 18 FDA reports)
AORTIC VALVE DISEASE ( 18 FDA reports)
APLASIA PURE RED CELL ( 18 FDA reports)
APPLICATION SITE REACTION ( 18 FDA reports)
ASPERGILLOSIS ( 18 FDA reports)
BLADDER DYSFUNCTION ( 18 FDA reports)
BLOOD UREA DECREASED ( 18 FDA reports)
BLOOD URIC ACID INCREASED ( 18 FDA reports)
BONE MARROW OEDEMA ( 18 FDA reports)
BOWEL SOUNDS ABNORMAL ( 18 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 18 FDA reports)
CARDIAC HYPERTROPHY ( 18 FDA reports)
CATHETER RELATED COMPLICATION ( 18 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 18 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 18 FDA reports)
CHRONIC FATIGUE SYNDROME ( 18 FDA reports)
CONGENITAL ANOMALY ( 18 FDA reports)
DIABETES INSIPIDUS ( 18 FDA reports)
EAR NEOPLASM ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 18 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 18 FDA reports)
EPIDURAL LIPOMATOSIS ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
EYE OEDEMA ( 18 FDA reports)
FEEDING DISORDER NEONATAL ( 18 FDA reports)
FOOD POISONING ( 18 FDA reports)
FUNGAEMIA ( 18 FDA reports)
GLOBULINS INCREASED ( 18 FDA reports)
HELICOBACTER GASTRITIS ( 18 FDA reports)
HIP SURGERY ( 18 FDA reports)
HUNGER ( 18 FDA reports)
HYPERURICAEMIA ( 18 FDA reports)
IMPETIGO ( 18 FDA reports)
JUDGEMENT IMPAIRED ( 18 FDA reports)
MACROGLOSSIA ( 18 FDA reports)
METABOLIC ALKALOSIS ( 18 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 18 FDA reports)
NERVE ROOT LESION ( 18 FDA reports)
NIKOLSKY'S SIGN ( 18 FDA reports)
OROPHARYNGEAL BLISTERING ( 18 FDA reports)
PAPILLOMA ( 18 FDA reports)
PENILE PAIN ( 18 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 18 FDA reports)
POST-TRAUMATIC PAIN ( 18 FDA reports)
RADICULITIS ( 18 FDA reports)
RADIUS FRACTURE ( 18 FDA reports)
RECTAL FISSURE ( 18 FDA reports)
RENAL COLIC ( 18 FDA reports)
RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
SKIN INFECTION ( 18 FDA reports)
SPINAL DEFORMITY ( 18 FDA reports)
STRABISMUS ( 18 FDA reports)
STRIDOR ( 18 FDA reports)
TESTICULAR SWELLING ( 18 FDA reports)
THERMAL BURN ( 18 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 18 FDA reports)
TRAUMATIC BRAIN INJURY ( 18 FDA reports)
URETHRAL OBSTRUCTION ( 18 FDA reports)
URINARY TRACT DISORDER ( 18 FDA reports)
PAROTID GLAND ENLARGEMENT ( 17 FDA reports)
PATELLA FRACTURE ( 17 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 17 FDA reports)
POLYTRAUMATISM ( 17 FDA reports)
PRESSURE OF SPEECH ( 17 FDA reports)
PSORIATIC ARTHROPATHY ( 17 FDA reports)
QUALITY OF LIFE DECREASED ( 17 FDA reports)
RESPIRATORY ALKALOSIS ( 17 FDA reports)
RETINAL HAEMORRHAGE ( 17 FDA reports)
SCOTOMA ( 17 FDA reports)
STASIS DERMATITIS ( 17 FDA reports)
TEMPORAL ARTERITIS ( 17 FDA reports)
VERTEBROPLASTY ( 17 FDA reports)
VOMITING PROJECTILE ( 17 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 17 FDA reports)
ADRENAL NEOPLASM ( 17 FDA reports)
ALCOHOL ABUSE ( 17 FDA reports)
ALCOHOL INTERACTION ( 17 FDA reports)
AORTIC DISSECTION ( 17 FDA reports)
AXILLARY MASS ( 17 FDA reports)
BILIARY CYST ( 17 FDA reports)
BLINDNESS TRANSIENT ( 17 FDA reports)
BLOOD CHLORIDE INCREASED ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 17 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 17 FDA reports)
BREAST LUMP REMOVAL ( 17 FDA reports)
CARDIOPULMONARY FAILURE ( 17 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 17 FDA reports)
CATHETER RELATED INFECTION ( 17 FDA reports)
CHARLES BONNET SYNDROME ( 17 FDA reports)
COLON CANCER RECURRENT ( 17 FDA reports)
EAR HAEMORRHAGE ( 17 FDA reports)
EARLY SATIETY ( 17 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 17 FDA reports)
EROSIVE OESOPHAGITIS ( 17 FDA reports)
ESCHERICHIA TEST POSITIVE ( 17 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 17 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 17 FDA reports)
FOREIGN BODY ( 17 FDA reports)
GALLBLADDER INJURY ( 17 FDA reports)
GASTROINTESTINAL PERFORATION ( 17 FDA reports)
GENITAL RASH ( 17 FDA reports)
HAIR TEXTURE ABNORMAL ( 17 FDA reports)
INFUSION SITE REACTION ( 17 FDA reports)
INJECTION SITE IRRITATION ( 17 FDA reports)
KIDNEY SMALL ( 17 FDA reports)
LIBIDO INCREASED ( 17 FDA reports)
LIP ULCERATION ( 17 FDA reports)
LUNG CANCER METASTATIC ( 17 FDA reports)
LYMPHADENITIS ( 17 FDA reports)
LYMPHOCYTOSIS ( 17 FDA reports)
MECHANICAL VENTILATION ( 17 FDA reports)
METASTATIC PAIN ( 17 FDA reports)
MUCOUS MEMBRANE DISORDER ( 17 FDA reports)
MYASTHENIA GRAVIS ( 17 FDA reports)
NARCOLEPSY ( 17 FDA reports)
NEURODERMATITIS ( 17 FDA reports)
NEUROENDOCRINE CARCINOMA ( 17 FDA reports)
NEUTROPENIC COLITIS ( 17 FDA reports)
OBSESSIVE THOUGHTS ( 17 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 16 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
ARTHROPOD BITE ( 16 FDA reports)
ASPIRATION JOINT ( 16 FDA reports)
BLADDER HYPERTROPHY ( 16 FDA reports)
BLOOD MAGNESIUM INCREASED ( 16 FDA reports)
BUNDLE BRANCH BLOCK ( 16 FDA reports)
CARBON DIOXIDE DECREASED ( 16 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 16 FDA reports)
CARDIAC FLUTTER ( 16 FDA reports)
CATHETER PLACEMENT ( 16 FDA reports)
CEREBRAL DISORDER ( 16 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 16 FDA reports)
CHEMOTHERAPY ( 16 FDA reports)
CHOLESTEROSIS ( 16 FDA reports)
CLUMSINESS ( 16 FDA reports)
COARCTATION OF THE AORTA ( 16 FDA reports)
COLPOCELE ( 16 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 16 FDA reports)
CUBITAL TUNNEL SYNDROME ( 16 FDA reports)
CUTIS LAXA ( 16 FDA reports)
DYSHIDROSIS ( 16 FDA reports)
DYSMENORRHOEA ( 16 FDA reports)
DYSPLASIA ( 16 FDA reports)
ENTEROBACTER INFECTION ( 16 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 16 FDA reports)
FEMORAL NECK FRACTURE ( 16 FDA reports)
FURUNCLE ( 16 FDA reports)
GLIOBLASTOMA MULTIFORME ( 16 FDA reports)
HYPERMETROPIA ( 16 FDA reports)
HYPEROSMOLAR STATE ( 16 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 16 FDA reports)
IATROGENIC INJURY ( 16 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 16 FDA reports)
INJECTION SITE URTICARIA ( 16 FDA reports)
JOINT CONTRACTURE ( 16 FDA reports)
KELOID SCAR ( 16 FDA reports)
LIVEDO RETICULARIS ( 16 FDA reports)
MENIERE'S DISEASE ( 16 FDA reports)
METABOLIC SYNDROME ( 16 FDA reports)
METASTASES TO PLEURA ( 16 FDA reports)
ONYCHOMADESIS ( 16 FDA reports)
OPTIC NEURITIS ( 16 FDA reports)
OSTEOMA ( 16 FDA reports)
PAIN OF SKIN ( 16 FDA reports)
PANCREATIC CARCINOMA ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
PARAPARESIS ( 16 FDA reports)
POOR PERSONAL HYGIENE ( 16 FDA reports)
POOR SUCKING REFLEX ( 16 FDA reports)
POST CONCUSSION SYNDROME ( 16 FDA reports)
POST HERPETIC NEURALGIA ( 16 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 16 FDA reports)
RADIATION OESOPHAGITIS ( 16 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 16 FDA reports)
RENAL TUBULAR ACIDOSIS ( 16 FDA reports)
SKIN IRRITATION ( 16 FDA reports)
SPINAL COLUMN INJURY ( 16 FDA reports)
SPINAL CORD INJURY ( 16 FDA reports)
SYSTEMIC CANDIDA ( 16 FDA reports)
TOE AMPUTATION ( 16 FDA reports)
TONGUE COATED ( 16 FDA reports)
TOOTH DISCOLOURATION ( 16 FDA reports)
UNDERDOSE ( 16 FDA reports)
VASCULAR INJURY ( 16 FDA reports)
VEIN DISORDER ( 16 FDA reports)
VENOUS OCCLUSION ( 16 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 16 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 15 FDA reports)
PERITONEAL EFFUSION ( 15 FDA reports)
PERITONITIS BACTERIAL ( 15 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 15 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 15 FDA reports)
POSTICTAL STATE ( 15 FDA reports)
POSTNASAL DRIP ( 15 FDA reports)
PULMONARY CALCIFICATION ( 15 FDA reports)
PULMONARY TOXICITY ( 15 FDA reports)
RETINAL DETACHMENT ( 15 FDA reports)
RETINOPATHY ( 15 FDA reports)
SINUS ARRHYTHMIA ( 15 FDA reports)
SKIN FIBROSIS ( 15 FDA reports)
SKULL FRACTURE ( 15 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 15 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 15 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 15 FDA reports)
TONGUE INJURY ( 15 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 15 FDA reports)
TRACHEITIS ( 15 FDA reports)
TRANSFUSION REACTION ( 15 FDA reports)
UTERINE CANCER ( 15 FDA reports)
WOUND SECRETION ( 15 FDA reports)
ABDOMINAL ADHESIONS ( 15 FDA reports)
ABSCESS LIMB ( 15 FDA reports)
ADRENAL MASS ( 15 FDA reports)
ANORECTAL DISORDER ( 15 FDA reports)
APPLICATION SITE IRRITATION ( 15 FDA reports)
APPLICATION SITE RASH ( 15 FDA reports)
ATRIAL TACHYCARDIA ( 15 FDA reports)
BACTERIAL TEST POSITIVE ( 15 FDA reports)
BLADDER PAIN ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
BLOOD TEST ABNORMAL ( 15 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 15 FDA reports)
BRADYPNOEA ( 15 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 15 FDA reports)
CUSHING'S SYNDROME ( 15 FDA reports)
DELUSION OF GRANDEUR ( 15 FDA reports)
DIABETIC GASTROPARESIS ( 15 FDA reports)
DIVERTICULAR PERFORATION ( 15 FDA reports)
ECZEMA ASTEATOTIC ( 15 FDA reports)
ENDOMETRIOSIS ( 15 FDA reports)
EOSINOPHIL COUNT DECREASED ( 15 FDA reports)
ESCHERICHIA SEPSIS ( 15 FDA reports)
EYE INFECTION ( 15 FDA reports)
FIBROADENOMA OF BREAST ( 15 FDA reports)
FIBROMA ( 15 FDA reports)
FOETAL GROWTH RETARDATION ( 15 FDA reports)
GALLBLADDER POLYP ( 15 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 15 FDA reports)
HAEMANGIOMA OF LIVER ( 15 FDA reports)
HEPATIC ENZYME ABNORMAL ( 15 FDA reports)
HYPERAEMIA ( 15 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 15 FDA reports)
ILIAC ARTERY THROMBOSIS ( 15 FDA reports)
INCISION SITE INFECTION ( 15 FDA reports)
INJECTION SITE NODULE ( 15 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 15 FDA reports)
INTESTINAL RESECTION ( 15 FDA reports)
INTRACARDIAC THROMBUS ( 15 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 15 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 15 FDA reports)
JUGULAR VEIN THROMBOSIS ( 15 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 15 FDA reports)
LABORATORY TEST INTERFERENCE ( 15 FDA reports)
LACTOSE INTOLERANCE ( 15 FDA reports)
LARGE INTESTINAL ULCER ( 15 FDA reports)
LIP EROSION ( 15 FDA reports)
METASTASES TO MENINGES ( 15 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 15 FDA reports)
MYELOMA RECURRENCE ( 15 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 15 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 15 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 15 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 14 FDA reports)
ABSCESS NECK ( 14 FDA reports)
ABSCESS ORAL ( 14 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 14 FDA reports)
ACCOMMODATION DISORDER ( 14 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 14 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 14 FDA reports)
ANTICHOLINERGIC SYNDROME ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 14 FDA reports)
APGAR SCORE LOW ( 14 FDA reports)
ARTHRITIS BACTERIAL ( 14 FDA reports)
BALANITIS ( 14 FDA reports)
BIOPSY BONE MARROW ( 14 FDA reports)
BLADDER CATHETERISATION ( 14 FDA reports)
BLADDER CYST ( 14 FDA reports)
BLOOD BICARBONATE INCREASED ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BLOOD DISORDER ( 14 FDA reports)
BLOOD LACTIC ACID INCREASED ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
BRONCHIAL INFECTION ( 14 FDA reports)
BULIMIA NERVOSA ( 14 FDA reports)
CARCINOID SYNDROME ( 14 FDA reports)
CARDIOTOXICITY ( 14 FDA reports)
CULTURE WOUND POSITIVE ( 14 FDA reports)
DENTAL PLAQUE ( 14 FDA reports)
DEVICE OCCLUSION ( 14 FDA reports)
DEVICE RELATED SEPSIS ( 14 FDA reports)
DRUG TOLERANCE INCREASED ( 14 FDA reports)
DYSPNOEA AT REST ( 14 FDA reports)
EJECTION FRACTION ( 14 FDA reports)
ENCEPHALITIS HERPES ( 14 FDA reports)
ENERGY INCREASED ( 14 FDA reports)
FOOD INTOLERANCE ( 14 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 14 FDA reports)
GAZE PALSY ( 14 FDA reports)
GLYCOSURIA ( 14 FDA reports)
HAEMOGLOBIN INCREASED ( 14 FDA reports)
HANGOVER ( 14 FDA reports)
HYPERCOAGULATION ( 14 FDA reports)
HYPERPYREXIA ( 14 FDA reports)
HYPERSEXUALITY ( 14 FDA reports)
HYPOGONADISM ( 14 FDA reports)
ICHTHYOSIS ( 14 FDA reports)
ILEITIS ( 14 FDA reports)
INFECTED SEBACEOUS CYST ( 14 FDA reports)
INFECTIOUS PERITONITIS ( 14 FDA reports)
INHIBITORY DRUG INTERACTION ( 14 FDA reports)
INJECTION SITE DISCOLOURATION ( 14 FDA reports)
INTRA-UTERINE DEATH ( 14 FDA reports)
LISTLESS ( 14 FDA reports)
LYMPHOCELE ( 14 FDA reports)
MARITAL PROBLEM ( 14 FDA reports)
MIDDLE EAR EFFUSION ( 14 FDA reports)
MOANING ( 14 FDA reports)
MYOCARDIAL FIBROSIS ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NEPHROSCLEROSIS ( 14 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 14 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
ORAL FUNGAL INFECTION ( 14 FDA reports)
ORAL MUCOSA ATROPHY ( 14 FDA reports)
ORAL MUCOSAL BLISTERING ( 14 FDA reports)
ORAL SOFT TISSUE DISORDER ( 14 FDA reports)
ORCHITIS ( 14 FDA reports)
ORTHODONTIC APPLIANCE USER ( 14 FDA reports)
PORIOMANIA ( 14 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 14 FDA reports)
POST PROCEDURAL INFECTION ( 14 FDA reports)
PRINZMETAL ANGINA ( 14 FDA reports)
RADIATION SKIN INJURY ( 14 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 14 FDA reports)
RENAL TUBULAR DISORDER ( 14 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 14 FDA reports)
SECRETION DISCHARGE ( 14 FDA reports)
SHOCK HAEMORRHAGIC ( 14 FDA reports)
SKIN ATROPHY ( 14 FDA reports)
SKIN HYPERPIGMENTATION ( 14 FDA reports)
SLOW RESPONSE TO STIMULI ( 14 FDA reports)
SUPERINFECTION ( 14 FDA reports)
THROAT CANCER ( 14 FDA reports)
THYROID CYST ( 14 FDA reports)
TINEA CRURIS ( 14 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 14 FDA reports)
WATER INTOXICATION ( 14 FDA reports)
PARKINSONIAN GAIT ( 13 FDA reports)
PERINEAL PAIN ( 13 FDA reports)
PERONEAL NERVE PALSY ( 13 FDA reports)
PINGUECULA ( 13 FDA reports)
PO2 INCREASED ( 13 FDA reports)
POST PROCEDURAL PAIN ( 13 FDA reports)
POTENTIATING DRUG INTERACTION ( 13 FDA reports)
PROTHROMBIN TIME SHORTENED ( 13 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 13 FDA reports)
RECURRENT CANCER ( 13 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 13 FDA reports)
REFLEXES ABNORMAL ( 13 FDA reports)
REFLUX LARYNGITIS ( 13 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 13 FDA reports)
RENAL ARTERY STENOSIS ( 13 FDA reports)
SALPINGO-OOPHORECTOMY ( 13 FDA reports)
SCRATCH ( 13 FDA reports)
SKIN DESQUAMATION ( 13 FDA reports)
SNEEZING ( 13 FDA reports)
SPINAL LAMINECTOMY ( 13 FDA reports)
SPONDYLITIS ( 13 FDA reports)
STENT OCCLUSION ( 13 FDA reports)
TERMINAL STATE ( 13 FDA reports)
THROMBOCYTOPENIC PURPURA ( 13 FDA reports)
TINEA PEDIS ( 13 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 13 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 13 FDA reports)
TRIGEMINAL NEURALGIA ( 13 FDA reports)
TRIGGER FINGER ( 13 FDA reports)
VASCULAR DEMENTIA ( 13 FDA reports)
WEST NILE VIRAL INFECTION ( 13 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 13 FDA reports)
ADNEXA UTERI MASS ( 13 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 13 FDA reports)
ANAEMIA POSTOPERATIVE ( 13 FDA reports)
APHONIA ( 13 FDA reports)
ARTERIAL DISORDER ( 13 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 13 FDA reports)
ATONIC SEIZURES ( 13 FDA reports)
BEZOAR ( 13 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 13 FDA reports)
BK VIRUS INFECTION ( 13 FDA reports)
BLADDER DIVERTICULUM ( 13 FDA reports)
BLOOD CORTISOL DECREASED ( 13 FDA reports)
BONE MARROW DISORDER ( 13 FDA reports)
BRAIN CONTUSION ( 13 FDA reports)
BREAST ENLARGEMENT ( 13 FDA reports)
BREAST SWELLING ( 13 FDA reports)
CAPILLARY LEAK SYNDROME ( 13 FDA reports)
CARDIAC ASTHMA ( 13 FDA reports)
CATHETER SITE HAEMATOMA ( 13 FDA reports)
CATHETER SITE HAEMORRHAGE ( 13 FDA reports)
CEREBRAL HAEMATOMA ( 13 FDA reports)
COLON POLYPECTOMY ( 13 FDA reports)
COMMINUTED FRACTURE ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
DIPLEGIA ( 13 FDA reports)
DYSPNOEA EXACERBATED ( 13 FDA reports)
EAR DISCOMFORT ( 13 FDA reports)
ENTEROCUTANEOUS FISTULA ( 13 FDA reports)
EXOPHTHALMOS ( 13 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 13 FDA reports)
GALLBLADDER OPERATION ( 13 FDA reports)
GASTRIC PERFORATION ( 13 FDA reports)
GLIOSIS ( 13 FDA reports)
GLUCOSE URINE PRESENT ( 13 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 13 FDA reports)
HEPATITIS B ( 13 FDA reports)
HOARSENESS ( 13 FDA reports)
HYPERCHLORHYDRIA ( 13 FDA reports)
HYPERVISCOSITY SYNDROME ( 13 FDA reports)
HYPOPNOEA ( 13 FDA reports)
HYPOREFLEXIA ( 13 FDA reports)
INCISIONAL HERNIA ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
KETONURIA ( 13 FDA reports)
LUNG ADENOCARCINOMA ( 13 FDA reports)
LUNG OPERATION ( 13 FDA reports)
MEAN CELL VOLUME INCREASED ( 13 FDA reports)
MENINGITIS CHEMICAL ( 13 FDA reports)
MICTURITION DISORDER ( 13 FDA reports)
MUCOSAL DRYNESS ( 13 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 13 FDA reports)
NEPHRITIC SYNDROME ( 13 FDA reports)
NEUROFIBROMA ( 13 FDA reports)
NEUROPATHIC ULCER ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
NICOTINE DEPENDENCE ( 13 FDA reports)
OESOPHAGEAL CARCINOMA ( 13 FDA reports)
ORAL NEOPLASM ( 13 FDA reports)
ORGAN FAILURE ( 13 FDA reports)
OVARIAN MASS ( 13 FDA reports)
PAIN EXACERBATED ( 13 FDA reports)
PARADOXICAL DRUG REACTION ( 13 FDA reports)
ADRENAL HAEMORRHAGE ( 12 FDA reports)
ADVERSE REACTION ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
APHAKIA ( 12 FDA reports)
BACTERIAL TOXAEMIA ( 12 FDA reports)
BLADDER CALCULUS REMOVAL ( 12 FDA reports)
BLOOD FOLATE INCREASED ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 12 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 12 FDA reports)
BONE MARROW TOXICITY ( 12 FDA reports)
BONE SARCOMA ( 12 FDA reports)
BRAIN MASS ( 12 FDA reports)
BREAST RECONSTRUCTION ( 12 FDA reports)
BRONCHITIS BACTERIAL ( 12 FDA reports)
CALCINOSIS ( 12 FDA reports)
CALCULUS URETERIC ( 12 FDA reports)
CARDIAC OPERATION ( 12 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 12 FDA reports)
CAUDA EQUINA SYNDROME ( 12 FDA reports)
CEREBELLAR SYNDROME ( 12 FDA reports)
CHEST WALL PAIN ( 12 FDA reports)
CLAUSTROPHOBIA ( 12 FDA reports)
COLONIC STENOSIS ( 12 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 12 FDA reports)
CORNEAL ABRASION ( 12 FDA reports)
DEPRESSION SUICIDAL ( 12 FDA reports)
DUODENOGASTRIC REFLUX ( 12 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 12 FDA reports)
DYSPAREUNIA ( 12 FDA reports)
ENGRAFTMENT SYNDROME ( 12 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 12 FDA reports)
EYE ALLERGY ( 12 FDA reports)
EYE DISCHARGE ( 12 FDA reports)
FOLATE DEFICIENCY ( 12 FDA reports)
FOLLICULITIS ( 12 FDA reports)
FUNGAL SKIN INFECTION ( 12 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 12 FDA reports)
GASTRIC BYPASS ( 12 FDA reports)
GENERALISED ANXIETY DISORDER ( 12 FDA reports)
GLOMERULONEPHRITIS ( 12 FDA reports)
GRIMACING ( 12 FDA reports)
HAIR COLOUR CHANGES ( 12 FDA reports)
HEART DISEASE CONGENITAL ( 12 FDA reports)
HEPATORENAL FAILURE ( 12 FDA reports)
HORMONE LEVEL ABNORMAL ( 12 FDA reports)
HYPERMETABOLISM ( 12 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 12 FDA reports)
IMPULSE-CONTROL DISORDER ( 12 FDA reports)
INDIFFERENCE ( 12 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 12 FDA reports)
INTRACRANIAL HYPOTENSION ( 12 FDA reports)
IRITIS ( 12 FDA reports)
LICHEN PLANUS ( 12 FDA reports)
MEDIASTINAL DISORDER ( 12 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 12 FDA reports)
MICTURITION FREQUENCY DECREASED ( 12 FDA reports)
MUSCLE FATIGUE ( 12 FDA reports)
MYELOCYTE COUNT INCREASED ( 12 FDA reports)
MYOTONIA ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
NASAL SINUS CANCER ( 12 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 12 FDA reports)
OESOPHAGEAL RUPTURE ( 12 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 12 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PANCREATIC NEOPLASM ( 12 FDA reports)
PANCREATIC PSEUDOCYST ( 12 FDA reports)
PARACHUTE MITRAL VALVE ( 12 FDA reports)
PCO2 INCREASED ( 12 FDA reports)
PERIODONTAL OPERATION ( 12 FDA reports)
PERIORBITAL OEDEMA ( 12 FDA reports)
PLASTIC SURGERY TO THE FACE ( 12 FDA reports)
PNEUMOPERITONEUM ( 12 FDA reports)
POSTURING ( 12 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 12 FDA reports)
PREMENSTRUAL SYNDROME ( 12 FDA reports)
PRIAPISM ( 12 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 12 FDA reports)
PSYCHOTIC BEHAVIOUR ( 12 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 12 FDA reports)
PULMONARY INFARCTION ( 12 FDA reports)
RECTAL PROLAPSE ( 12 FDA reports)
RETINOPATHY HYPERTENSIVE ( 12 FDA reports)
RETROPERITONEAL HAEMATOMA ( 12 FDA reports)
SELF MUTILATION ( 12 FDA reports)
SKIN TURGOR DECREASED ( 12 FDA reports)
STEREOTYPY ( 12 FDA reports)
STRESS INCONTINENCE ( 12 FDA reports)
THERAPY CESSATION ( 12 FDA reports)
TOOTH EROSION ( 12 FDA reports)
TUMOUR HAEMORRHAGE ( 12 FDA reports)
VASCULAR PSEUDOANEURYSM ( 12 FDA reports)
VESTIBULAR DISORDER ( 12 FDA reports)
VULVAL DISORDER ( 12 FDA reports)
YAWNING ( 12 FDA reports)
PARTNER STRESS ( 11 FDA reports)
PERIARTHRITIS ( 11 FDA reports)
PHARYNGEAL ERYTHEMA ( 11 FDA reports)
POLYARTHRITIS ( 11 FDA reports)
PORTAL VEIN THROMBOSIS ( 11 FDA reports)
POST THROMBOTIC SYNDROME ( 11 FDA reports)
PROSTATE TENDERNESS ( 11 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
PSEUDODEMENTIA ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RECTAL POLYP ( 11 FDA reports)
RENAL CANCER ( 11 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
SENILE OSTEOPOROSIS ( 11 FDA reports)
SHOULDER ARTHROPLASTY ( 11 FDA reports)
SJOGREN'S SYNDROME ( 11 FDA reports)
SKIN INJURY ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SOFT TISSUE INFECTION ( 11 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 11 FDA reports)
STARVATION ( 11 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 11 FDA reports)
SUBCUTANEOUS NODULE ( 11 FDA reports)
TERATOMA ( 11 FDA reports)
TIC ( 11 FDA reports)
URTICARIA GENERALISED ( 11 FDA reports)
UTERINE PROLAPSE ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VENA CAVA THROMBOSIS ( 11 FDA reports)
WALKING DISABILITY ( 11 FDA reports)
WEIGHT LOSS POOR ( 11 FDA reports)
ABDOMINAL INFECTION ( 11 FDA reports)
ABSCESS INTESTINAL ( 11 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 11 FDA reports)
AMBLYOPIA ( 11 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 11 FDA reports)
ANAL FISSURE ( 11 FDA reports)
ANAL SPHINCTER ATONY ( 11 FDA reports)
ANTISOCIAL BEHAVIOUR ( 11 FDA reports)
AORTIC ATHEROSCLEROSIS ( 11 FDA reports)
APICAL GRANULOMA ( 11 FDA reports)
APPARENT DEATH ( 11 FDA reports)
APPENDICECTOMY ( 11 FDA reports)
APRAXIA ( 11 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 11 FDA reports)
ARTHRITIS INFECTIVE ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
BACTERIA URINE IDENTIFIED ( 11 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 11 FDA reports)
BLADDER SPASM ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 11 FDA reports)
BRADYARRHYTHMIA ( 11 FDA reports)
BRAIN COMPRESSION ( 11 FDA reports)
BRAIN DAMAGE ( 11 FDA reports)
CALCIPHYLAXIS ( 11 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 11 FDA reports)
CARDIAC ANEURYSM ( 11 FDA reports)
CARDIAC OUTPUT DECREASED ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
CATARACT NUCLEAR ( 11 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 11 FDA reports)
CHEST INJURY ( 11 FDA reports)
CHOLESTATIC LIVER INJURY ( 11 FDA reports)
COCCIDIOIDOMYCOSIS ( 11 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 11 FDA reports)
CORONARY ARTERY BYPASS ( 11 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 11 FDA reports)
DEATH OF RELATIVE ( 11 FDA reports)
DELUSIONAL PERCEPTION ( 11 FDA reports)
DISSOCIATIVE FUGUE ( 11 FDA reports)
DIURETIC THERAPY ( 11 FDA reports)
DUODENAL POLYP ( 11 FDA reports)
DYSPHASIA ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
EMBOLIC STROKE ( 11 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 11 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 11 FDA reports)
EPIDIDYMAL CYST ( 11 FDA reports)
ERYTHEMA OF EYELID ( 11 FDA reports)
EYE INJURY ( 11 FDA reports)
FACIAL NERVE DISORDER ( 11 FDA reports)
FAT EMBOLISM ( 11 FDA reports)
FAT NECROSIS ( 11 FDA reports)
FOOD AVERSION ( 11 FDA reports)
FOOT OPERATION ( 11 FDA reports)
FOREIGN BODY TRAUMA ( 11 FDA reports)
GAMBLING ( 11 FDA reports)
GAMMOPATHY ( 11 FDA reports)
GENERALISED ERYTHEMA ( 11 FDA reports)
GINGIVAL GRAFT ( 11 FDA reports)
HEART INJURY ( 11 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 11 FDA reports)
HYDROPNEUMOTHORAX ( 11 FDA reports)
HYPERACUSIS ( 11 FDA reports)
HYPHAEMA ( 11 FDA reports)
HYPOCOAGULABLE STATE ( 11 FDA reports)
HYPOTONIA NEONATAL ( 11 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 11 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 11 FDA reports)
INJECTION SITE EXTRAVASATION ( 11 FDA reports)
INJECTION SITE MASS ( 11 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 11 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 11 FDA reports)
JOINT CREPITATION ( 11 FDA reports)
KIDNEY ENLARGEMENT ( 11 FDA reports)
LEGAL PROBLEM ( 11 FDA reports)
LIP BLISTER ( 11 FDA reports)
LIPIDS INCREASED ( 11 FDA reports)
LUNG INJURY ( 11 FDA reports)
LUPUS-LIKE SYNDROME ( 11 FDA reports)
LYMPHATIC OBSTRUCTION ( 11 FDA reports)
MACULOPATHY ( 11 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 11 FDA reports)
MEIBOMIANITIS ( 11 FDA reports)
METAPLASIA ( 11 FDA reports)
MONOPARESIS ( 11 FDA reports)
MULTIPLE ALLERGIES ( 11 FDA reports)
MYELITIS ( 11 FDA reports)
NAIL DYSTROPHY ( 11 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 11 FDA reports)
NEUROSIS ( 11 FDA reports)
NODAL ARRHYTHMIA ( 11 FDA reports)
NONSPECIFIC REACTION ( 11 FDA reports)
OCULAR HYPERTENSION ( 11 FDA reports)
OLIGOHYDRAMNIOS ( 11 FDA reports)
OPEN REDUCTION OF FRACTURE ( 11 FDA reports)
OPPORTUNISTIC INFECTION ( 11 FDA reports)
PARAPSORIASIS ( 11 FDA reports)
PARATHYROID TUMOUR BENIGN ( 11 FDA reports)
ABNORMAL FAECES ( 10 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 10 FDA reports)
ADENOTONSILLECTOMY ( 10 FDA reports)
ALVEOLOPLASTY ( 10 FDA reports)
AMIMIA ( 10 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANTIBODY TEST POSITIVE ( 10 FDA reports)
ARTHROSCOPIC SURGERY ( 10 FDA reports)
ASTERIXIS ( 10 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 10 FDA reports)
BENIGN BREAST LUMP REMOVAL ( 10 FDA reports)
BLADDER DILATATION ( 10 FDA reports)
BLOOD ALBUMIN INCREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 10 FDA reports)
BLOOD OESTROGEN INCREASED ( 10 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 10 FDA reports)
BONE CYST ( 10 FDA reports)
BONE GRAFT ( 10 FDA reports)
BONE MARROW DEPRESSION ( 10 FDA reports)
BRAIN OPERATION ( 10 FDA reports)
CALCULUS URINARY ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
CELLULITIS ORBITAL ( 10 FDA reports)
CENTRAL LINE INFECTION ( 10 FDA reports)
CEREBELLAR HAEMORRHAGE ( 10 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 10 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 10 FDA reports)
CHOKING SENSATION ( 10 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 10 FDA reports)
COMPULSIVE SHOPPING ( 10 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 10 FDA reports)
CORNEAL REFLEX DECREASED ( 10 FDA reports)
CRANIOCEREBRAL INJURY ( 10 FDA reports)
CYSTITIS NONINFECTIVE ( 10 FDA reports)
CYSTOPEXY ( 10 FDA reports)
DEFAECATION URGENCY ( 10 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 10 FDA reports)
DEVICE LEAKAGE ( 10 FDA reports)
DIABETIC MICROANGIOPATHY ( 10 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 10 FDA reports)
DUODENAL ULCER PERFORATION ( 10 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 10 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 10 FDA reports)
ENTEROCOCCAL SEPSIS ( 10 FDA reports)
EXCESSIVE EYE BLINKING ( 10 FDA reports)
EXTREMITY CONTRACTURE ( 10 FDA reports)
FALLOT'S TETRALOGY ( 10 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 10 FDA reports)
GENITAL HERPES ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
HAEMOCHROMATOSIS ( 10 FDA reports)
HAEMOGLOBIN ABNORMAL ( 10 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HERPES VIRUS INFECTION ( 10 FDA reports)
HYDROURETER ( 10 FDA reports)
HYPOGLYCAEMIC COMA ( 10 FDA reports)
INFUSION SITE INFECTION ( 10 FDA reports)
INJECTION SITE BRUISING ( 10 FDA reports)
INJECTION SITE RASH ( 10 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 10 FDA reports)
JAW CYST ( 10 FDA reports)
JOINT LOCK ( 10 FDA reports)
KERATOACANTHOMA ( 10 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 10 FDA reports)
LARGE FOR DATES BABY ( 10 FDA reports)
LIGAMENT INJURY ( 10 FDA reports)
LINEAR IGA DISEASE ( 10 FDA reports)
MACULE ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
MENISCUS REMOVAL ( 10 FDA reports)
MITRAL VALVE REPAIR ( 10 FDA reports)
MONARTHRITIS ( 10 FDA reports)
MONOCYTE COUNT DECREASED ( 10 FDA reports)
NASAL TURBINATE ABNORMALITY ( 10 FDA reports)
NEOPLASM SKIN ( 10 FDA reports)
NEUROENDOCRINE TUMOUR ( 10 FDA reports)
OBSTRUCTION ( 10 FDA reports)
OCULAR ICTERUS ( 10 FDA reports)
OCULOGYRATION ( 10 FDA reports)
OESOPHAGEAL ATRESIA ( 10 FDA reports)
OSTEOSARCOMA METASTATIC ( 10 FDA reports)
PANCREATIC ENZYMES INCREASED ( 10 FDA reports)
PARATHYROIDECTOMY ( 10 FDA reports)
PEMPHIGOID ( 10 FDA reports)
PERITONEAL DIALYSIS ( 10 FDA reports)
PHIMOSIS ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PLEURAL ADHESION ( 10 FDA reports)
PLEURAL DISORDER ( 10 FDA reports)
POISONING DELIBERATE ( 10 FDA reports)
POLYP COLORECTAL ( 10 FDA reports)
POSTOPERATIVE INFECTION ( 10 FDA reports)
PRODUCT TASTE ABNORMAL ( 10 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 10 FDA reports)
PYELOCALIECTASIS ( 10 FDA reports)
QUADRIPLEGIA ( 10 FDA reports)
REGURGITATION ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
SALIVARY GLAND DISORDER ( 10 FDA reports)
SEBACEOUS GLAND DISORDER ( 10 FDA reports)
SEROSITIS ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
SIALOADENITIS ( 10 FDA reports)
SKIN ODOUR ABNORMAL ( 10 FDA reports)
SKIN PAPILLOMA ( 10 FDA reports)
SLEEP WALKING ( 10 FDA reports)
SPINAL FUSION SURGERY ( 10 FDA reports)
SPLEEN CONGESTION ( 10 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 10 FDA reports)
THOUGHT BLOCKING ( 10 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 10 FDA reports)
TORTICOLLIS ( 10 FDA reports)
TRAUMATIC HAEMATOMA ( 10 FDA reports)
TREATMENT FAILURE ( 10 FDA reports)
TROPONIN T INCREASED ( 10 FDA reports)
UMBILICAL CORD ABNORMALITY ( 10 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 10 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 10 FDA reports)
URINE ANALYSIS ABNORMAL ( 10 FDA reports)
UTERINE MASS ( 10 FDA reports)
VAGINAL CANDIDIASIS ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VASCULAR OPERATION ( 10 FDA reports)
VITAMIN K DEFICIENCY ( 10 FDA reports)
VULVOVAGINAL PAIN ( 10 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 10 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERICARDIAL DISEASE ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
PLEURECTOMY ( 9 FDA reports)
PNEUMONIA KLEBSIELLA ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
POLYSUBSTANCE ABUSE ( 9 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 9 FDA reports)
PRECANCEROUS CELLS PRESENT ( 9 FDA reports)
PRODUCT TAMPERING ( 9 FDA reports)
PROSTATIC DISORDER ( 9 FDA reports)
PRURITUS GENITAL ( 9 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 9 FDA reports)
PULSE ABNORMAL ( 9 FDA reports)
RECALL PHENOMENON ( 9 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 9 FDA reports)
RENAL ISCHAEMIA ( 9 FDA reports)
RETICULOCYTOSIS ( 9 FDA reports)
RETINAL ISCHAEMIA ( 9 FDA reports)
RHABDOMYOSARCOMA ( 9 FDA reports)
RHINITIS SEASONAL ( 9 FDA reports)
SHUNT INFECTION ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SKIN PLAQUE ( 9 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 9 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 9 FDA reports)
STEATORRHOEA ( 9 FDA reports)
SYSTEMIC SCLEROSIS ( 9 FDA reports)
SYSTOLIC HYPERTENSION ( 9 FDA reports)
TEMPORAL LOBE EPILEPSY ( 9 FDA reports)
THERAPEUTIC PROCEDURE ( 9 FDA reports)
THREATENED LABOUR ( 9 FDA reports)
THYROXINE INCREASED ( 9 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 9 FDA reports)
TRACHEAL ATRESIA ( 9 FDA reports)
ULCERATIVE KERATITIS ( 9 FDA reports)
ULNAR NERVE INJURY ( 9 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 9 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 9 FDA reports)
URETERAL NEOPLASM ( 9 FDA reports)
URETHRAL PAIN ( 9 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 9 FDA reports)
URINE OUTPUT ( 9 FDA reports)
UVEITIS ( 9 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 9 FDA reports)
VASOSPASM ( 9 FDA reports)
VERBAL ABUSE ( 9 FDA reports)
VITAMIN B12 DECREASED ( 9 FDA reports)
VOCAL CORD DISORDER ( 9 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 9 FDA reports)
ANAL HAEMORRHAGE ( 9 FDA reports)
ANAL PRURITUS ( 9 FDA reports)
ANDROGENS ABNORMAL ( 9 FDA reports)
ANOSMIA ( 9 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
APALLIC SYNDROME ( 9 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 9 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 9 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
ATROPHIC VULVOVAGINITIS ( 9 FDA reports)
BELLIGERENCE ( 9 FDA reports)
BILE DUCT CANCER ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLEEDING TIME PROLONGED ( 9 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BLOOD IRON INCREASED ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BRAIN MIDLINE SHIFT ( 9 FDA reports)
BRAIN STEM INFARCTION ( 9 FDA reports)
BREAST CANCER IN SITU ( 9 FDA reports)
CARDIAC VALVE ABSCESS ( 9 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CERUMEN REMOVAL ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHRONIC HEPATITIS ( 9 FDA reports)
COAGULATION TIME PROLONGED ( 9 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 9 FDA reports)
COLORECTAL CANCER METASTATIC ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CULTURE POSITIVE ( 9 FDA reports)
DISINHIBITION ( 9 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 9 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 9 FDA reports)
EJACULATION FAILURE ( 9 FDA reports)
ELECTRIC SHOCK ( 9 FDA reports)
ELEVATED MOOD ( 9 FDA reports)
EMBOLISM ARTERIAL ( 9 FDA reports)
ERYTHROPENIA ( 9 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 9 FDA reports)
EXCITABILITY ( 9 FDA reports)
FEELING HOT AND COLD ( 9 FDA reports)
FEELINGS OF WORTHLESSNESS ( 9 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 9 FDA reports)
FOREIGN BODY ASPIRATION ( 9 FDA reports)
FREEZING PHENOMENON ( 9 FDA reports)
GALLBLADDER ENLARGEMENT ( 9 FDA reports)
GASTROENTERITIS SALMONELLA ( 9 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 9 FDA reports)
HAEMANGIOMA CONGENITAL ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPERVIGILANCE ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
HYPOVITAMINOSIS ( 9 FDA reports)
IMMUNE SYSTEM DISORDER ( 9 FDA reports)
INFARCTION ( 9 FDA reports)
INTESTINAL STENOSIS ( 9 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 9 FDA reports)
LARYNGOSCOPY ( 9 FDA reports)
LYMPH NODE CALCIFICATION ( 9 FDA reports)
MUSCLE MASS ( 9 FDA reports)
NECROTISING COLITIS ( 9 FDA reports)
NEONATAL ASPHYXIA ( 9 FDA reports)
NERVE ROOT COMPRESSION ( 9 FDA reports)
NEUROMYOPATHY ( 9 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 9 FDA reports)
OESOPHAGEAL DILATATION ( 9 FDA reports)
OPEN ANGLE GLAUCOMA ( 9 FDA reports)
OPTIC NERVE DISORDER ( 9 FDA reports)
OROPHARYNGEAL SWELLING ( 9 FDA reports)
PANCREATIC INSUFFICIENCY ( 9 FDA reports)
ABDOMINAL SEPSIS ( 8 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACTINOMYCES TEST POSITIVE ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
ADDISON'S DISEASE ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 8 FDA reports)
AMNESTIC DISORDER ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
ANASTOMOTIC LEAK ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
ANKYLOSING SPONDYLITIS ( 8 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
AORTIC THROMBOSIS ( 8 FDA reports)
ARTERIAL STENOSIS ( 8 FDA reports)
ASTHENOPIA ( 8 FDA reports)
AURICULAR SWELLING ( 8 FDA reports)
AUTOIMMUNE THYROIDITIS ( 8 FDA reports)
AUTONOMIC NEUROPATHY ( 8 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BILIARY NEOPLASM ( 8 FDA reports)
BLADDER CANCER RECURRENT ( 8 FDA reports)
BLADDER DISTENSION ( 8 FDA reports)
BLADDER OPERATION ( 8 FDA reports)
BLOOD ALCOHOL INCREASED ( 8 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 8 FDA reports)
BLOOD URIC ACID DECREASED ( 8 FDA reports)
BLOOD URINE ( 8 FDA reports)
BONE FORMATION DECREASED ( 8 FDA reports)
BREAST FIBROSIS ( 8 FDA reports)
BRONCHIAL OBSTRUCTION ( 8 FDA reports)
BRONCHIAL SECRETION RETENTION ( 8 FDA reports)
CALCIFICATION OF MUSCLE ( 8 FDA reports)
CAMPYLOBACTER INFECTION ( 8 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CARDIAC FAILURE CHRONIC ( 8 FDA reports)
CARDIOVERSION ( 8 FDA reports)
CATHETER SITE PAIN ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 8 FDA reports)
CEREBROSCLEROSIS ( 8 FDA reports)
CHEMICAL INJURY ( 8 FDA reports)
CHOREOATHETOSIS ( 8 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 8 FDA reports)
CLEFT PALATE ( 8 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
COAGULATION FACTOR DECREASED ( 8 FDA reports)
COMPARTMENT SYNDROME ( 8 FDA reports)
COMPULSIONS ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 8 FDA reports)
CONTRAST MEDIA REACTION ( 8 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
CRYPTOPHTHALMOS ( 8 FDA reports)
CSF PROTEIN INCREASED ( 8 FDA reports)
CSF SHUNT REMOVAL ( 8 FDA reports)
CUSHINGOID ( 8 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 8 FDA reports)
DISEASE COMPLICATION ( 8 FDA reports)
DISSOCIATIVE DISORDER ( 8 FDA reports)
DRUG RESISTANCE ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ERYSIPELAS ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
FAECES HARD ( 8 FDA reports)
GALLBLADDER PAIN ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
GASTRODUODENITIS ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 8 FDA reports)
GASTROINTESTINAL TOXICITY ( 8 FDA reports)
GESTATIONAL DIABETES ( 8 FDA reports)
GINGIVAL ABSCESS ( 8 FDA reports)
GINGIVAL OPERATION ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HAND DEFORMITY ( 8 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 8 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HORDEOLUM ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPERKINESIA ( 8 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 8 FDA reports)
HYPERTROPHY ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
INFERTILITY MALE ( 8 FDA reports)
INJECTION SITE WARMTH ( 8 FDA reports)
INSULIN RESISTANCE ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 8 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
KLEBSIELLA SEPSIS ( 8 FDA reports)
LEUKODYSTROPHY ( 8 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 8 FDA reports)
LIPOATROPHY ( 8 FDA reports)
LOCALISED OEDEMA ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
MAXILLOFACIAL OPERATION ( 8 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 8 FDA reports)
MEGACOLON ( 8 FDA reports)
MENINGEAL DISORDER ( 8 FDA reports)
MENSTRUATION DELAYED ( 8 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 8 FDA reports)
METASTASES TO PERITONEUM ( 8 FDA reports)
MICROALBUMINURIA ( 8 FDA reports)
MONOCYTOSIS ( 8 FDA reports)
MOUTH INJURY ( 8 FDA reports)
MULTI-ORGAN DISORDER ( 8 FDA reports)
MYELOPATHY ( 8 FDA reports)
NAIL DISCOLOURATION ( 8 FDA reports)
NECROTISING FASCIITIS ( 8 FDA reports)
NEPHRECTOMY ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 8 FDA reports)
NOSOCOMIAL INFECTION ( 8 FDA reports)
OBSTRUCTION GASTRIC ( 8 FDA reports)
OMENTECTOMY ( 8 FDA reports)
ONYCHOCLASIS ( 8 FDA reports)
OOPHORECTOMY ( 8 FDA reports)
ORTHOSTATIC HYPERTENSION ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 8 FDA reports)
PARAPROTEINAEMIA ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PENILE PROSTHESIS INSERTION ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PERIORBITAL CELLULITIS ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
PHOBIA ( 8 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 8 FDA reports)
POLYCYTHAEMIA ( 8 FDA reports)
POLYHYDRAMNIOS ( 8 FDA reports)
POOR VENOUS ACCESS ( 8 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
PREMATURE EJACULATION ( 8 FDA reports)
PRODUCT FORMULATION ISSUE ( 8 FDA reports)
PROSTATIC CALCIFICATION ( 8 FDA reports)
PSYCHOLOGICAL TRAUMA ( 8 FDA reports)
PULMONARY HYPOPLASIA ( 8 FDA reports)
PULMONARY MYCOSIS ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
READING DISORDER ( 8 FDA reports)
RECTAL PERFORATION ( 8 FDA reports)
RECTAL ULCER ( 8 FDA reports)
RENAL ARTERIOSCLEROSIS ( 8 FDA reports)
RENAL HYPERTROPHY ( 8 FDA reports)
RETINAL SCAR ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SHIFT TO THE LEFT ( 8 FDA reports)
SKULL FRACTURED BASE ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SOCIAL PHOBIA ( 8 FDA reports)
SOMATIC DELUSION ( 8 FDA reports)
SPINAL HAEMANGIOMA ( 8 FDA reports)
SPINAL PAIN ( 8 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 8 FDA reports)
SUDDEN ONSET OF SLEEP ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
TETANY ( 8 FDA reports)
THYROIDECTOMY ( 8 FDA reports)
TOXIC SHOCK SYNDROME ( 8 FDA reports)
URINE OUTPUT INCREASED ( 8 FDA reports)
URINE SODIUM DECREASED ( 8 FDA reports)
VAGINAL CYST ( 8 FDA reports)
VAGINITIS BACTERIAL ( 8 FDA reports)
VASCULAR PURPURA ( 8 FDA reports)
VASCULITIS NECROTISING ( 8 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
VICTIM OF SEXUAL ABUSE ( 8 FDA reports)
VIRAL LABYRINTHITIS ( 8 FDA reports)
VULVAL ABSCESS ( 8 FDA reports)
WEANING FAILURE ( 8 FDA reports)
YELLOW SKIN ( 8 FDA reports)
PELVIC HAEMATOMA ( 7 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PHARYNGEAL DISORDER ( 7 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 7 FDA reports)
PHONOPHOBIA ( 7 FDA reports)
PIGMENTED NAEVUS ( 7 FDA reports)
PNEUMONIA FUNGAL ( 7 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 7 FDA reports)
POSTOPERATIVE ADHESION ( 7 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 7 FDA reports)
POSTPARTUM HAEMORRHAGE ( 7 FDA reports)
PREMATURE DELIVERY ( 7 FDA reports)
PROCEDURAL HYPOTENSION ( 7 FDA reports)
PROPOFOL INFUSION SYNDROME ( 7 FDA reports)
PROSTRATION ( 7 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 7 FDA reports)
PUPILLARY DISORDER ( 7 FDA reports)
RADIATION FIBROSIS - LUNG ( 7 FDA reports)
RADICULITIS LUMBOSACRAL ( 7 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 7 FDA reports)
RETINAL ARTERY OCCLUSION ( 7 FDA reports)
RETINOIC ACID SYNDROME ( 7 FDA reports)
SARCOMA ( 7 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 7 FDA reports)
SCLERODERMA ( 7 FDA reports)
SCROTAL SWELLING ( 7 FDA reports)
SEPTIC EMBOLUS ( 7 FDA reports)
SHARED PSYCHOTIC DISORDER ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN LESION EXCISION ( 7 FDA reports)
SPINAL CLAUDICATION ( 7 FDA reports)
SUBDURAL HAEMORRHAGE ( 7 FDA reports)
SUFFOCATION FEELING ( 7 FDA reports)
SWEAT DISCOLOURATION ( 7 FDA reports)
SYSTEMIC MYCOSIS ( 7 FDA reports)
TALIPES ( 7 FDA reports)
TENDON OPERATION ( 7 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 7 FDA reports)
THYMUS DISORDER ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
TOOTH HYPOPLASIA ( 7 FDA reports)
TRACHEAL INJURY ( 7 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 7 FDA reports)
ULNA FRACTURE ( 7 FDA reports)
UMBILICAL HERNIA REPAIR ( 7 FDA reports)
URINE KETONE BODY PRESENT ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 7 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 7 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 7 FDA reports)
ABORTION ( 7 FDA reports)
ACANTHOLYSIS ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
ACUTE LEUKAEMIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
ALLERGY TO CHEMICALS ( 7 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 7 FDA reports)
ANAEMIA MACROCYTIC ( 7 FDA reports)
ANAL FISTULA ( 7 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 7 FDA reports)
AORTIC VALVE STENOSIS ( 7 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 7 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 7 FDA reports)
B-CELL LYMPHOMA ( 7 FDA reports)
BALLISMUS ( 7 FDA reports)
BASOPHIL COUNT INCREASED ( 7 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BIPOLAR II DISORDER ( 7 FDA reports)
BITE ( 7 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 7 FDA reports)
BLOOD CREATININE ABNORMAL ( 7 FDA reports)
BLOOD OESTROGEN DECREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 7 FDA reports)
BONE NEOPLASM ( 7 FDA reports)
BREAST ABSCESS ( 7 FDA reports)
BREAST DISCHARGE ( 7 FDA reports)
BREAST DISORDER ( 7 FDA reports)
BRONCHIAL FISTULA ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BRONCHOPLEURAL FISTULA ( 7 FDA reports)
BURN OF INTERNAL ORGANS ( 7 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CARBON DIOXIDE INCREASED ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 7 FDA reports)
CARNITINE DECREASED ( 7 FDA reports)
CATHETER SITE INFECTION ( 7 FDA reports)
CEREBELLAR ATROPHY ( 7 FDA reports)
CERVIX CARCINOMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHRONIC TONSILLITIS ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
COLONIC OBSTRUCTION ( 7 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 7 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 7 FDA reports)
DENTAL NECROSIS ( 7 FDA reports)
DERMATITIS ATOPIC ( 7 FDA reports)
DIAPHRAGMATIC HERNIA ( 7 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 7 FDA reports)
DROP ATTACKS ( 7 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 7 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
ELECTROCONVULSIVE THERAPY ( 7 FDA reports)
ENTEROVESICAL FISTULA ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
FEAR OF DEATH ( 7 FDA reports)
FEEDING TUBE COMPLICATION ( 7 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 7 FDA reports)
FINGER DEFORMITY ( 7 FDA reports)
FLASHBACK ( 7 FDA reports)
FLOPPY INFANT ( 7 FDA reports)
FRACTURED COCCYX ( 7 FDA reports)
GASTRIC MUCOSAL LESION ( 7 FDA reports)
GOUTY ARTHRITIS ( 7 FDA reports)
GRANDIOSITY ( 7 FDA reports)
GRANULOCYTE COUNT DECREASED ( 7 FDA reports)
GRANULOCYTE COUNT INCREASED ( 7 FDA reports)
GUILLAIN-BARRE SYNDROME ( 7 FDA reports)
HAEMANGIOMA OF SKIN ( 7 FDA reports)
HAEMOGLOBINURIA ( 7 FDA reports)
HAEMORRHAGE URINARY TRACT ( 7 FDA reports)
HAIR DISORDER ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEAD BANGING ( 7 FDA reports)
HEAD TITUBATION ( 7 FDA reports)
HEART RATE ABNORMAL ( 7 FDA reports)
HEART SOUNDS ABNORMAL ( 7 FDA reports)
HEMIANOPIA ( 7 FDA reports)
HERPES ZOSTER DISSEMINATED ( 7 FDA reports)
HIDRADENITIS ( 7 FDA reports)
HISTOPLASMOSIS ( 7 FDA reports)
HYPERTHERMIA MALIGNANT ( 7 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 7 FDA reports)
INCREASED BRONCHIAL SECRETION ( 7 FDA reports)
INFUSION SITE PAIN ( 7 FDA reports)
INJECTION SITE PAPULE ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 7 FDA reports)
IRIS ADHESIONS ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
IRON OVERLOAD ( 7 FDA reports)
JOINT INJECTION ( 7 FDA reports)
LAPAROTOMY ( 7 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 7 FDA reports)
LIGAMENT DISORDER ( 7 FDA reports)
LIMB MALFORMATION ( 7 FDA reports)
LIP HAEMORRHAGE ( 7 FDA reports)
LIP PAIN ( 7 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
LYMPH NODE PALPABLE ( 7 FDA reports)
LYMPHOCYTIC INFILTRATION ( 7 FDA reports)
MENINGITIS VIRAL ( 7 FDA reports)
MENOPAUSAL SYMPTOMS ( 7 FDA reports)
METAMORPHOPSIA ( 7 FDA reports)
METASTASES TO MOUTH ( 7 FDA reports)
METASTASES TO SPLEEN ( 7 FDA reports)
METASTATIC CARCINOID TUMOUR ( 7 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 7 FDA reports)
MICROCEPHALY ( 7 FDA reports)
MONONEURITIS ( 7 FDA reports)
MOTION SICKNESS ( 7 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 7 FDA reports)
NASAL DRYNESS ( 7 FDA reports)
NEGATIVE THOUGHTS ( 7 FDA reports)
NEGATIVISM ( 7 FDA reports)
NODULE ON EXTREMITY ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 7 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 7 FDA reports)
OESOPHAGITIS ULCERATIVE ( 7 FDA reports)
ORAL TORUS ( 7 FDA reports)
ORBITAL OEDEMA ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
ORGASMIC SENSATION DECREASED ( 7 FDA reports)
OSTEITIS DEFORMANS ( 7 FDA reports)
OSTEOMYELITIS CHRONIC ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OVARIAN CANCER RECURRENT ( 7 FDA reports)
PARACENTESIS ( 7 FDA reports)
PARAKERATOSIS ( 7 FDA reports)
PARALYSIS FLACCID ( 7 FDA reports)
PARESIS ( 7 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ABSCESS RUPTURE ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 6 FDA reports)
ADENOVIRUS INFECTION ( 6 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 6 FDA reports)
AEROMONA INFECTION ( 6 FDA reports)
AMINO ACID LEVEL INCREASED ( 6 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
APHERESIS ( 6 FDA reports)
APLASIA ( 6 FDA reports)
APPLICATION SITE BURN ( 6 FDA reports)
APPLICATION SITE PAIN ( 6 FDA reports)
ARACHNOIDITIS ( 6 FDA reports)
ARM AMPUTATION ( 6 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 6 FDA reports)
ASPERGER'S DISORDER ( 6 FDA reports)
AUTISM ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BENIGN BREAST NEOPLASM ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 6 FDA reports)
BIOPSY BREAST ABNORMAL ( 6 FDA reports)
BLOOD CALCIUM ABNORMAL ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 6 FDA reports)
BLOOD GLUCOSE ( 6 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 6 FDA reports)
BLUNTED AFFECT ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 6 FDA reports)
BURN INFECTION ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARDIAC PACEMAKER REVISION ( 6 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
CELL MARKER INCREASED ( 6 FDA reports)
CHEMICAL POISONING ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 6 FDA reports)
COMA SCALE ABNORMAL ( 6 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CONJUNCTIVAL ABRASION ( 6 FDA reports)
CONNECTIVE TISSUE DISORDER ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
CORRECTIVE LENS USER ( 6 FDA reports)
CORYNEBACTERIUM INFECTION ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CYST ASPIRATION ( 6 FDA reports)
CYSTITIS INTERSTITIAL ( 6 FDA reports)
DAYDREAMING ( 6 FDA reports)
DEAFNESS UNILATERAL ( 6 FDA reports)
DELIRIUM TREMENS ( 6 FDA reports)
DENTAL PULP DISORDER ( 6 FDA reports)
DERMATILLOMANIA ( 6 FDA reports)
DEVICE ADHESION ISSUE ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DROWNING ( 6 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 6 FDA reports)
ENANTHEMA ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
ERECTION INCREASED ( 6 FDA reports)
EXERCISE TOLERANCE DECREASED ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
EXTERNAL EAR CELLULITIS ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
FALLOPIAN TUBE OPERATION ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
FUNGAL SEPSIS ( 6 FDA reports)
FUNGAL TEST POSITIVE ( 6 FDA reports)
GALLBLADDER OEDEMA ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 6 FDA reports)
HEPATIC HAEMORRHAGE ( 6 FDA reports)
HEPATIC SIDEROSIS ( 6 FDA reports)
HEPATIC TRAUMA ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HISTONE ANTIBODY POSITIVE ( 6 FDA reports)
HYPERMAGNESAEMIA ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 6 FDA reports)
INFANTILE APNOEIC ATTACK ( 6 FDA reports)
INFECTED DERMAL CYST ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
KAPOSI'S SARCOMA ( 6 FDA reports)
KERATOCONUS ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
LATEX ALLERGY ( 6 FDA reports)
LEUKAEMIA PLASMACYTIC ( 6 FDA reports)
LIVER TENDERNESS ( 6 FDA reports)
LORDOSIS ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
MACROCEPHALY ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 6 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 6 FDA reports)
MELANOSIS COLI ( 6 FDA reports)
MENINGITIS BACTERIAL ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
MENOPAUSE ( 6 FDA reports)
METHAEMOGLOBINAEMIA ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 6 FDA reports)
MYCOSIS FUNGOIDES ( 6 FDA reports)
MYOCLONIC EPILEPSY ( 6 FDA reports)
NASAL VESTIBULITIS ( 6 FDA reports)
NIPPLE PAIN ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
OOPHORECTOMY BILATERAL ( 6 FDA reports)
OSTEOCALCIN INCREASED ( 6 FDA reports)
OVARIAN CANCER METASTATIC ( 6 FDA reports)
OVARIAN ENLARGEMENT ( 6 FDA reports)
OXYGEN SATURATION ABNORMAL ( 6 FDA reports)
PALATAL DISORDER ( 6 FDA reports)
PALMAR ERYTHEMA ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PERIRECTAL ABSCESS ( 6 FDA reports)
PEYRONIE'S DISEASE ( 6 FDA reports)
PITUITARY TUMOUR BENIGN ( 6 FDA reports)
PNEUMONIA LEGIONELLA ( 6 FDA reports)
POIKILOCYTOSIS ( 6 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 6 FDA reports)
POLYMYOSITIS ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 6 FDA reports)
PROCEDURAL SITE REACTION ( 6 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 6 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 6 FDA reports)
PULMONARY EOSINOPHILIA ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 6 FDA reports)
PYURIA ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
RED MAN SYNDROME ( 6 FDA reports)
REGRESSIVE BEHAVIOUR ( 6 FDA reports)
RENAL CELL CARCINOMA ( 6 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 6 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 6 FDA reports)
RETINAL DISORDER ( 6 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
SEXUAL ABUSE ( 6 FDA reports)
SMALL FOR DATES BABY ( 6 FDA reports)
SMOKER ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
SPLENIC LESION ( 6 FDA reports)
STAB WOUND ( 6 FDA reports)
STENOTROPHOMONAS INFECTION ( 6 FDA reports)
SUPERINFECTION BACTERIAL ( 6 FDA reports)
SYNOVIAL RUPTURE ( 6 FDA reports)
TELANGIECTASIA ( 6 FDA reports)
THYROID CANCER METASTATIC ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 6 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 6 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URETHRAL STRICTURE ( 6 FDA reports)
URGE INCONTINENCE ( 6 FDA reports)
VARICELLA ( 6 FDA reports)
VASCULAR ENCEPHALOPATHY ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 6 FDA reports)
VIRAEMIA ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
VOCAL CORD THICKENING ( 6 FDA reports)
WEIGHT BEARING DIFFICULTY ( 6 FDA reports)
WOUND DECOMPOSITION ( 6 FDA reports)
WOUND HAEMORRHAGE ( 6 FDA reports)
X-RAY ABNORMAL ( 6 FDA reports)
PATIENT RESTRAINT ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 5 FDA reports)
PERITONEAL DISORDER ( 5 FDA reports)
PHAEOCHROMOCYTOMA ( 5 FDA reports)
PHLEBOLITH ( 5 FDA reports)
PLATELET AGGREGATION INCREASED ( 5 FDA reports)
PNEUMONIA NECROTISING ( 5 FDA reports)
POLYMEDICATION ( 5 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 5 FDA reports)
PORTAL VEIN OCCLUSION ( 5 FDA reports)
POST PROCEDURAL CELLULITIS ( 5 FDA reports)
POST PROCEDURAL DISCHARGE ( 5 FDA reports)
POSTPARTUM DEPRESSION ( 5 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PSYCHOMOTOR AGITATION ( 5 FDA reports)
PSYCHOSOMATIC DISEASE ( 5 FDA reports)
PULMONARY CAVITATION ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY SARCOIDOSIS ( 5 FDA reports)
PYLORIC STENOSIS ( 5 FDA reports)
PYOTHORAX ( 5 FDA reports)
RADIATION INJURY ( 5 FDA reports)
RECTAL TENESMUS ( 5 FDA reports)
REITER'S SYNDROME ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RETINAL VEIN OCCLUSION ( 5 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 5 FDA reports)
SALPINGITIS ( 5 FDA reports)
SEBORRHOEA ( 5 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 5 FDA reports)
SHOULDER OPERATION ( 5 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 5 FDA reports)
SINUS ARREST ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 5 FDA reports)
SLEEP-RELATED EATING DISORDER ( 5 FDA reports)
SLOW SPEECH ( 5 FDA reports)
SOFT TISSUE NECROSIS ( 5 FDA reports)
SOMNOLENCE NEONATAL ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
SPUTUM PURULENT ( 5 FDA reports)
STATUS MIGRAINOSUS ( 5 FDA reports)
SUPERINFECTION LUNG ( 5 FDA reports)
SUSPICIOUSNESS ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 5 FDA reports)
TAENIASIS ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
TENOSYNOVITIS STENOSANS ( 5 FDA reports)
THYROID MASS ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TONGUE SPASM ( 5 FDA reports)
TONIC CONVULSION ( 5 FDA reports)
TONSILLAR DISORDER ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 5 FDA reports)
TRACHEAL OEDEMA ( 5 FDA reports)
TRANSFERRIN INCREASED ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
URETHRITIS ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
VASCULAR GRAFT ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
VASCULAR OCCLUSION ( 5 FDA reports)
VERTEBRAL COLUMN MASS ( 5 FDA reports)
VICTIM OF CRIME ( 5 FDA reports)
VITILIGO ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
ABDOMINAL INJURY ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ACTIVATION SYNDROME ( 5 FDA reports)
AIR EMBOLISM ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ALCOHOL PROBLEM ( 5 FDA reports)
AMAUROSIS ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANORGASMIA ( 5 FDA reports)
ANOXIA ( 5 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AORTIC DISORDER ( 5 FDA reports)
APPLICATION SITE DERMATITIS ( 5 FDA reports)
APPLICATION SITE VESICLES ( 5 FDA reports)
APTYALISM ( 5 FDA reports)
ARTERIAL THROMBOSIS ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ASPIRATION BRONCHIAL ( 5 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 5 FDA reports)
AURA ( 5 FDA reports)
AXILLARY VEIN THROMBOSIS ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BIFASCICULAR BLOCK ( 5 FDA reports)
BLADDER MASS ( 5 FDA reports)
BLADDER PERFORATION ( 5 FDA reports)
BLINDNESS CORTICAL ( 5 FDA reports)
BLOOD AMYLASE DECREASED ( 5 FDA reports)
BLOOD CORTISOL INCREASED ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD PRESSURE ( 5 FDA reports)
BRAIN STEM STROKE ( 5 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 5 FDA reports)
BRONCHIAL WALL THICKENING ( 5 FDA reports)
BURNING MOUTH SYNDROME ( 5 FDA reports)
BURNOUT SYNDROME ( 5 FDA reports)
CARCINOMA ( 5 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CATECHOLAMINES URINE INCREASED ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 5 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
COLLAGEN DISORDER ( 5 FDA reports)
COLONOSCOPY ( 5 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 5 FDA reports)
CONGENITAL PNEUMONIA ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CORONA VIRUS INFECTION ( 5 FDA reports)
CORONARY ARTERY EMBOLISM ( 5 FDA reports)
CRANIAL NERVE DISORDER ( 5 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 5 FDA reports)
DANDY-WALKER SYNDROME ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELUSIONS ( 5 FDA reports)
DENTAL CLEANING ( 5 FDA reports)
DENTAL PROSTHESIS USER ( 5 FDA reports)
DIAPHRAGMATIC DISORDER ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 5 FDA reports)
DISTRACTIBILITY ( 5 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
ECTOPIC PREGNANCY ( 5 FDA reports)
EJECTION FRACTION ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 5 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 5 FDA reports)
ENCEPHALITIS ALLERGIC ( 5 FDA reports)
ENCEPHALITIS VIRAL ( 5 FDA reports)
ENDOCARDITIS BACTERIAL ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ENTEROSTOMY ( 5 FDA reports)
ERYTHEMA MIGRANS ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EXTERNAL EAR INFLAMMATION ( 5 FDA reports)
EYE INFECTION VIRAL ( 5 FDA reports)
EYE LASER SURGERY ( 5 FDA reports)
FEMORAL ARTERY OCCLUSION ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
FUNGAL OESOPHAGITIS ( 5 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 5 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 5 FDA reports)
GASTROINTESTINAL CARCINOMA ( 5 FDA reports)
GASTROINTESTINAL ULCER ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HEAT STROKE ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HIRSUTISM ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HOFFMANN'S SIGN ( 5 FDA reports)
HUNTINGTON'S DISEASE ( 5 FDA reports)
HYPERTONIA NEONATAL ( 5 FDA reports)
HYPERTROPHY BREAST ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 5 FDA reports)
HYPOKINESIA NEONATAL ( 5 FDA reports)
HYPOTHYROIDIC GOITRE ( 5 FDA reports)
ILIAC ARTERY STENOSIS ( 5 FDA reports)
ILLUSION ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
IMPLANT EXPULSION ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
INADEQUATE DIET ( 5 FDA reports)
INFUSION SITE ERYTHEMA ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 5 FDA reports)
KLEBSIELLA TEST POSITIVE ( 5 FDA reports)
LEARNING DISORDER ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 5 FDA reports)
LIP DISCOLOURATION ( 5 FDA reports)
LIP DISORDER ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LOWER EXTREMITY MASS ( 5 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
NASAL NEOPLASM ( 5 FDA reports)
NASAL SEPTUM PERFORATION ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NEPHROBLASTOMA ( 5 FDA reports)
NERVE BLOCK ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEURODEGENERATIVE DISORDER ( 5 FDA reports)
NIGHT CRAMPS ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OCULOGYRIC CRISIS ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
ORAL MUCOSA EROSION ( 5 FDA reports)
OSMOLAR GAP ABNORMAL ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
OVARIAN EPITHELIAL CANCER ( 5 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 5 FDA reports)
OXYGEN SUPPLEMENTATION ( 5 FDA reports)
PAINFUL DEFAECATION ( 5 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARANOID PERSONALITY DISORDER ( 5 FDA reports)
PARASOMNIA ( 5 FDA reports)
ABULIA ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 4 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 4 FDA reports)
ADRENAL SUPPRESSION ( 4 FDA reports)
AGITATION NEONATAL ( 4 FDA reports)
ALCOHOLIC LIVER DISEASE ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ALLERGY TO ANIMAL ( 4 FDA reports)
AMMONIA ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
ANISOCYTOSIS ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
AORTIC INJURY ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BASAL GANGLIA INFARCTION ( 4 FDA reports)
BASE EXCESS DECREASED ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BLADDER DISCOMFORT ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 4 FDA reports)
BLOOD ETHANOL INCREASED ( 4 FDA reports)
BLOOD GASTRIN INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BLOOD VISCOSITY INCREASED ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 4 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
BRAIN STEM ISCHAEMIA ( 4 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
BUDD-CHIARI SYNDROME ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARBON MONOXIDE POISONING ( 4 FDA reports)
CARDIAC FIBRILLATION ( 4 FDA reports)
CARDIAC IMAGING PROCEDURE NORMAL ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 4 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
CIRRHOSIS ALCOHOLIC ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CLEFT LIP ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
COCCYDYNIA ( 4 FDA reports)
COGNITIVE DETERIORATION ( 4 FDA reports)
COLECTOMY TOTAL ( 4 FDA reports)
COLON CANCER STAGE III ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONGENITAL BLADDER ANOMALY ( 4 FDA reports)
CONGENITAL RENAL DISORDER ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CUTANEOUS VASCULITIS ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 4 FDA reports)
DERMATITIS HERPETIFORMIS ( 4 FDA reports)
DEVICE CONNECTION ISSUE ( 4 FDA reports)
DEVICE INTERACTION ( 4 FDA reports)
DIABETIC EYE DISEASE ( 4 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 4 FDA reports)
DISLOCATION OF VERTEBRA ( 4 FDA reports)
DIVORCED ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DYSKINESIA OESOPHAGEAL ( 4 FDA reports)
DYSPLASTIC NAEVUS ( 4 FDA reports)
DYSSOMNIA ( 4 FDA reports)
EARLY MORNING AWAKENING ( 4 FDA reports)
ECHOLALIA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
EMOTIONAL POVERTY ( 4 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 4 FDA reports)
ENCEPHALOMALACIA ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EPHELIDES ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYELASH DISCOLOURATION ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FLUID INTAKE RESTRICTION ( 4 FDA reports)
FOOT AMPUTATION ( 4 FDA reports)
FRACTURE DELAYED UNION ( 4 FDA reports)
FRACTURE DISPLACEMENT ( 4 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
GLARE ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOMERULOSCLEROSIS ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMISENSORY NEGLECT ( 4 FDA reports)
HEPATIC CALCIFICATION ( 4 FDA reports)
HEPATITIS A ( 4 FDA reports)
HEPATITIS A POSITIVE ( 4 FDA reports)
HERNIA HIATUS REPAIR ( 4 FDA reports)
HERPES OESOPHAGITIS ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPERTRICHOSIS ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
IMPLANT SITE INFECTION ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFLAMMATION OF WOUND ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INJECTION SITE OEDEMA ( 4 FDA reports)
INJECTION SITE STINGING ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INSTILLATION SITE ERYTHEMA ( 4 FDA reports)
INTERVERTEBRAL DISC INJURY ( 4 FDA reports)
INTESTINAL HYPOMOTILITY ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRAOSSEOUS ANGIOMA ( 4 FDA reports)
INTRAUTERINE INFECTION ( 4 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 4 FDA reports)
IRON DEFICIENCY ( 4 FDA reports)
JOINT ANKYLOSIS ( 4 FDA reports)
JOINT HYPEREXTENSION ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
LARYNGEAL CYST ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LIMB REDUCTION DEFECT ( 4 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 4 FDA reports)
LIP DRY ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIPID METABOLISM DISORDER ( 4 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 4 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 4 FDA reports)
MELAS SYNDROME ( 4 FDA reports)
METANEPHRINE URINE INCREASED ( 4 FDA reports)
METASTASES TO PANCREAS ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MICROCOCCUS INFECTION ( 4 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MIXED HYPERLIPIDAEMIA ( 4 FDA reports)
MIXED LIVER INJURY ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
MYELOFIBROSIS ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NASAL POLYPS ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
NIPPLE DISORDER ( 4 FDA reports)
NITRITE URINE PRESENT ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 4 FDA reports)
OROMANDIBULAR DYSTONIA ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OVARIAN DISORDER ( 4 FDA reports)
OXYGEN SATURATION ( 4 FDA reports)
PACEMAKER GENERATED RHYTHM ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANCREATITIS VIRAL ( 4 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 4 FDA reports)
PHOTODERMATOSIS ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PICA ( 4 FDA reports)
PLATELET COUNT ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PNEUMONIA HERPES VIRAL ( 4 FDA reports)
POST LAMINECTOMY SYNDROME ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POSTMENOPAUSE ( 4 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 4 FDA reports)
PROCEDURAL HYPERTENSION ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 4 FDA reports)
PSEUDOPARALYSIS ( 4 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 4 FDA reports)
PSYCHIATRIC INVESTIGATION ( 4 FDA reports)
PUBIS FRACTURE ( 4 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 4 FDA reports)
PULMONARY HILUM MASS ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
PULMONARY VASCULAR DISORDER ( 4 FDA reports)
PURPLE GLOVE SYNDROME ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RADIAL NERVE PALSY ( 4 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RENAL HAEMORRHAGE ( 4 FDA reports)
RESIDUAL URINE ( 4 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 4 FDA reports)
RESPIRATORY TRACT OEDEMA ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETINAL DEGENERATION ( 4 FDA reports)
RETINAL INJURY ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
RETROGRADE EJACULATION ( 4 FDA reports)
SALPINGOSTOMY ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCLERAL HAEMORRHAGE ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
SHORT-BOWEL SYNDROME ( 4 FDA reports)
SKIN INFLAMMATION ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 4 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
STRESS AT WORK ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUNBURN ( 4 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 4 FDA reports)
SURGICAL FAILURE ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
SYMBLEPHARON ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
TARSAL TUNNEL SYNDROME ( 4 FDA reports)
TEMPERATURE REGULATION DISORDER ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
THYROXINE DECREASED ( 4 FDA reports)
THYROXINE FREE INCREASED ( 4 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TORULOPSIS INFECTION ( 4 FDA reports)
TRANCE ( 4 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 4 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
TUBERCULOUS PLEURISY ( 4 FDA reports)
TUMOUR EXCISION ( 4 FDA reports)
TUMOUR INVASION ( 4 FDA reports)
TUMOUR MARKER INCREASED ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VASCULAR BYPASS GRAFT ( 4 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VESTIBULITIS ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VISUAL BRIGHTNESS ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VULVAL HAEMORRHAGE ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WAXY FLEXIBILITY ( 4 FDA reports)
WITHDRAWAL BLEED ( 4 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 4 FDA reports)
ZYGOMYCOSIS ( 4 FDA reports)
PARKINSONIAN REST TREMOR ( 3 FDA reports)
PAROTITIS ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 3 FDA reports)
PELVIC PROLAPSE ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERITONEAL ADHESIONS ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHARYNGEAL NEOPLASM ( 3 FDA reports)
PICKWICKIAN SYNDROME ( 3 FDA reports)
PIGMENTATION BUCCAL ( 3 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 3 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 3 FDA reports)
POSITIVE ROMBERGISM ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
POTTER'S SYNDROME ( 3 FDA reports)
POVERTY ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREALBUMIN DECREASED ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 3 FDA reports)
PROPHYLAXIS OF NAUSEA AND VOMITING ( 3 FDA reports)
PROSTATE CANCER RECURRENT ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PSYCHOSEXUAL DISORDER ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
PYROMANIA ( 3 FDA reports)
REACTION TO COLOURING ( 3 FDA reports)
REACTIVE PSYCHOSIS ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL NEOPLASM ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL FUNCTION TEST ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RETICULOCYTE COUNT INCREASED ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL TEAR ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RETINOPATHY CONGENITAL ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 3 FDA reports)
SCAPULA FRACTURE ( 3 FDA reports)
SCROTAL DISORDER ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SELECTIVE MUTISM ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SEPTOPLASTY ( 3 FDA reports)
SERRATIA TEST POSITIVE ( 3 FDA reports)
SEXUAL ACTIVITY INCREASED ( 3 FDA reports)
SHOULDER DEFORMITY ( 3 FDA reports)
SIGMOIDITIS ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN CANDIDA ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SPERMATOZOA ABNORMAL ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STENOTROPHOMONAS SEPSIS ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
TONGUE BLACK HAIRY ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRANSAMINASES ABNORMAL ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TROPONIN I ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
ULNAR NERVE PALSY ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER EXTREMITY MASS ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULITIS GASTROINTESTINAL ( 3 FDA reports)
VESSEL PERFORATION ( 3 FDA reports)
VICTIM OF ABUSE ( 3 FDA reports)
VICTIM OF HOMICIDE ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VOCAL CORD PARESIS ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
XEROPHTHALMIA ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ABORTION INFECTED ( 3 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACTINIC ELASTOSIS ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE STRESS DISORDER ( 3 FDA reports)
ADENOMYOSIS ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
AEROPHAGIA ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 3 FDA reports)
ALCOHOLIC PANCREATITIS ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGIOMYOLIPOMA ( 3 FDA reports)
ANORECTAL INFECTION ( 3 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBODY TEST ABNORMAL ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE EROSION ( 3 FDA reports)
APPLICATION SITE EXFOLIATION ( 3 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ARTERIAL STENT INSERTION ( 3 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
AVERSION ( 3 FDA reports)
BACILLARY ANGIOMATOSIS ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BENIGN TUMOUR EXCISION ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BIOPSY LIVER ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BIOPSY SKIN ABNORMAL ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID DECREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 3 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST CANCER STAGE IV ( 3 FDA reports)
BREAST OEDEMA ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
BRONCHIAL DISORDER ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BRONCHOSCOPY ( 3 FDA reports)
CAFFEINE CONSUMPTION ( 3 FDA reports)
CAMPTOCORMIA ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CAT SCRATCH DISEASE ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHEYNE-STOKES RESPIRATION ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHRONIC HEPATIC FAILURE ( 3 FDA reports)
CHYLOTHORAX ( 3 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
COLOUR BLINDNESS ( 3 FDA reports)
CONGENITAL UTERINE ANOMALY ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CORNEAL ABSCESS ( 3 FDA reports)
CORNEAL DEPOSITS ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
COTARD'S SYNDROME ( 3 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYCLOTHYMIC DISORDER ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYSTITIS RADIATION ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 3 FDA reports)
DELIVERY ( 3 FDA reports)
DELUSION OF REPLACEMENT ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DELUSIONAL DISORDER, SOMATIC TYPE ( 3 FDA reports)
DEPRESSIVE DELUSION ( 3 FDA reports)
DERMATITIS PAPILLARIS CAPILLITII ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DERMOGRAPHISM ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEVICE INTOLERANCE ( 3 FDA reports)
DEVICE MIGRATION ( 3 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 3 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG TOLERANCE DECREASED ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
EAR INFECTION FUNGAL ( 3 FDA reports)
EBSTEIN'S ANOMALY ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 3 FDA reports)
ENCHONDROMA ( 3 FDA reports)
ENDOCARDIAL FIBROSIS ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 3 FDA reports)
EOSINOPHILIC COLITIS ( 3 FDA reports)
EPILEPTIC AURA ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTUBATION ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FAECAL VOLUME DECREASED ( 3 FDA reports)
FASCIECTOMY ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 3 FDA reports)
FLAIL CHEST ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FOOD INTERACTION ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FULL BLOOD COUNT DECREASED ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GALLSTONE ILEUS ( 3 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 3 FDA reports)
GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
GASTROSTOMY ( 3 FDA reports)
GASTROSTOMY TUBE INSERTION ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GILBERT'S SYNDROME ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
GRANULOMA SKIN ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 3 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HALLUCINATION, OLFACTORY ( 3 FDA reports)
HALO VISION ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEPATITIS B DNA INCREASED ( 3 FDA reports)
HEPATITIS GRANULOMATOUS ( 3 FDA reports)
HERNIA CONGENITAL ( 3 FDA reports)
HOMELESS ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 3 FDA reports)
HUNTINGTON'S CHOREA ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERINSULINISM ( 3 FDA reports)
HYPERVITAMINOSIS ( 3 FDA reports)
HYPOLIPIDAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IIIRD NERVE PARESIS ( 3 FDA reports)
ILEOSTOMY ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
IMPLANT SITE EROSION ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE INDURATION ( 3 FDA reports)
INFUSION SITE RASH ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INJECTION SITE ANAESTHESIA ( 3 FDA reports)
INJECTION SITE ATROPHY ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTESTINAL ULCER ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JEJUNECTOMY ( 3 FDA reports)
JOINT ABSCESS ( 3 FDA reports)
JOINT ARTHROPLASTY ( 3 FDA reports)
JOINT WARMTH ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LACTOBACILLUS INFECTION ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LEUKOARAIOSIS ( 3 FDA reports)
LHERMITTE'S SIGN ( 3 FDA reports)
LIGAMENT PAIN ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LISTERIOSIS ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
MADAROSIS ( 3 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 3 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 3 FDA reports)
MAMMARY DUCT ECTASIA ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MASS EXCISION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEDICAL DIET ( 3 FDA reports)
MEIGE'S SYNDROME ( 3 FDA reports)
MENINGEAL NEOPLASM ( 3 FDA reports)
MENINGIOMA MALIGNANT ( 3 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 3 FDA reports)
MERALGIA PARAESTHETICA ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
METASTASES TO CHEST WALL ( 3 FDA reports)
METASTASES TO SMALL INTESTINE ( 3 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MIGRAINE WITHOUT AURA ( 3 FDA reports)
MINERAL METABOLISM DISORDER ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MORTON'S NEUROMA ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 3 FDA reports)
MYOFASCITIS ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASAL SEPTUM DISORDER ( 3 FDA reports)
NASAL SEPTUM ULCERATION ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NECROTISING RETINITIS ( 3 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 3 FDA reports)
NEOLOGISM ( 3 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 3 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 3 FDA reports)
NIPPLE EXUDATE BLOODY ( 3 FDA reports)
NODAL OSTEOARTHRITIS ( 3 FDA reports)
NORMAL DELIVERY ( 3 FDA reports)
NORMETANEPHRINE URINE INCREASED ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 3 FDA reports)
ON AND OFF PHENOMENON ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OSTECTOMY ( 3 FDA reports)
OSTEODYSTROPHY ( 3 FDA reports)
PALLIDOTOMY ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PARANASAL CYST ( 3 FDA reports)
5-HYDROXYINDOLACETIC ACID DECREASED ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE DECREASED ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL ANOMALY ( 2 FDA reports)
ABDOMINAL WALL CYST ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABORTION EARLY ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACOUSTIC NEUROMA ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACQUIRED TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
ACROCHORDON ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ACUTE POLYNEUROPATHY ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALCOHOLIC SEIZURE ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMMONIA ABNORMAL ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANGIOGRAM ABNORMAL ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANISOMETROPIA ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC THERAPY ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AUTOMATISM ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASOSQUAMOUS CARCINOMA OF SKIN ( 2 FDA reports)
BENIGN CARDIAC NEOPLASM ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE ABNORMAL ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BICARBONATE ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BODY DYSMORPHIC DISORDER ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREAST PROSTHESIS USER ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 2 FDA reports)
BUCCOGLOSSAL SYNDROME ( 2 FDA reports)
BURNING SENSATION MUCOSAL ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC INDEX INCREASED ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CARDITIS ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELLULITIS GANGRENOUS ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERULOPLASMIN DECREASED ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CERVIX CARCINOMA STAGE IV ( 2 FDA reports)
CHILD ABUSE ( 2 FDA reports)
CHOLANGITIS SCLEROSING ( 2 FDA reports)
CHOLANGITIS SUPPURATIVE ( 2 FDA reports)
CHOLINERGIC SYNDROME ( 2 FDA reports)
CHOROID PLEXUS PAPILLOMA ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON INJURY ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMA BLISTER ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 2 FDA reports)
CONGENITAL NEUROPATHY ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COOMBS TEST NEGATIVE ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
COUGH DECREASED ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRUSH SYNDROME ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
CYSTITIS GLANDULARIS ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEATH OF SIBLING ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEHYDROEPIANDROSTERONE TEST ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DEPOSIT EYE ( 2 FDA reports)
DEPRESSION POSTOPERATIVE ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DETOXIFICATION ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DEVICE LEAD DAMAGE ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DIABETIC ULCER ( 2 FDA reports)
DIET NONCOMPLIANCE ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG ADDICT ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG DIVERSION ( 2 FDA reports)
DRUG EFFECT DELAYED ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 2 FDA reports)
DRUG THERAPY CHANGED ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 2 FDA reports)
DUODENAL FISTULA ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
DYSPROSODY ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENCEPHALOCELE ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOMETRIAL ABLATION ( 2 FDA reports)
ENDOSCOPY ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
EOSINOPENIA ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIPHYSEAL DISORDER ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
EUTHANASIA ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EWING'S SARCOMA ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
EYE EXCISION ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEMALE STERILISATION ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL MOVEMENTS DECREASED ( 2 FDA reports)
FOETAL WARFARIN SYNDROME ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FRACTURED ISCHIUM ( 2 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC CYST ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC ULCER SURGERY ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRITIS VIRAL ( 2 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITOURINARY TRACT INFECTION ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GINGIVITIS ULCERATIVE ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBIN ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEART VALVE OPERATION ( 2 FDA reports)
HEART VALVE REPLACEMENT ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEPAPLASTIN ABNORMAL ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCREATINAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPNAGOGIC HALLUCINATION ( 2 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHONDRIASIS ( 2 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 2 FDA reports)
HYPONATRAEMIC SYNDROME ( 2 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOPHARYNGEAL CANCER ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
IDEAS OF REFERENCE ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
ILEOSTOMY CLOSURE ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE HAEMATOMA ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
IMPRISONMENT ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INFECTED LYMPHOCELE ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFLAMMATORY PAIN ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE CYST ( 2 FDA reports)
INJECTION SITE DISCOMFORT ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJURY CORNEAL ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTESTINAL ANASTOMOSIS ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL SPASM ( 2 FDA reports)
INTRACARDIAC MASS ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
ISOSPORIASIS ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
JOINT SURGERY ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABOUR PAIN ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LICE INFESTATION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIP HAEMATOMA ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOMA CUTIS ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MALE ORGASMIC DISORDER ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL DUCT ( 2 FDA reports)
MALIGNANT OLIGODENDROGLIOMA ( 2 FDA reports)
MASTOID DISORDER ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDICAL DEVICE REMOVAL ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS ENTEROCOCCAL ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 2 FDA reports)
MESENTERITIS ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTASES TO ABDOMINAL WALL ( 2 FDA reports)
METASTASES TO BLADDER ( 2 FDA reports)
METASTASES TO DIAPHRAGM ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METASTASES TO URINARY TRACT ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MITRAL VALVE DISEASE MIXED ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MUSCLE OPERATION ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
MYOSCLEROSIS ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
MYXOEDEMA COMA ( 2 FDA reports)
NAIL OPERATION ( 2 FDA reports)
NAIL TOXICITY ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL OPERATION ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL APNOEIC ATTACK ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL COMPLICATIONS OF SUBSTANCE ABUSE ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHRITIS AUTOIMMUNE ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NERVE ROOT INJURY ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL DISCOMFORT ( 2 FDA reports)
OESOPHAGEAL IRRITATION ( 2 FDA reports)
OESOPHAGEAL PERFORATION ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
ONYCHOLYSIS ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORCHITIS NONINFECTIVE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OTITIS MEDIA VIRAL ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVULATION PAIN ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PANCREAS DIVISUM ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC CARCINOMA STAGE II ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARACENTESIS ABDOMEN ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARENTERAL NUTRITION ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PENIS DISORDER ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL ADHESIONS DIVISION ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERITONSILLITIS ( 2 FDA reports)
PHARYNGEAL CANCER METASTATIC ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PHOBIA OF EXAMS ( 2 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 2 FDA reports)
PHOTOCOAGULATION ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PHYTOTHERAPY ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PITUITARY ENLARGEMENT ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLATELET PRODUCTION DECREASED ( 2 FDA reports)
PLATELET TOXICITY ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL INFECTION ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POLYARTERITIS NODOSA ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL DISCOMFORT ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST-TRAUMATIC EPILEPSY ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POVERTY OF THOUGHT CONTENT ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PRESCRIPTION FORM TAMPERING ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PRODUCT SIZE ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN CONSUMPTION TIME PROLONGED ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHIATRIC EVALUATION ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PSYCHOMOTOR SEIZURES ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
RADIATION ASSOCIATED PAIN ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RADIATION PNEUMONITIS ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 2 FDA reports)
RELATIONSHIP BREAKDOWN ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL DYSPLASIA ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE STRAIN INJURY ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RESTING TREMOR ( 2 FDA reports)
RETINAL ANEURYSM ( 2 FDA reports)
RETINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
RETINITIS VIRAL ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RHEUMATIC FEVER ( 2 FDA reports)
RHEUMATOID NODULE ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SACCADIC EYE MOVEMENT ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCHIZOPHRENIA SIMPLE ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHIGELLA INFECTION ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN MACERATION ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP PARALYSIS ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 2 FDA reports)
SPINAL MYELOGRAM ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLENITIS ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STENT MALFUNCTION ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBDURAL EFFUSION ( 2 FDA reports)
SUBRETINAL FIBROSIS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SUTURE REMOVAL ( 2 FDA reports)
SYMBOLIC DYSFUNCTION ( 2 FDA reports)
SYNOVIAL DISORDER ( 2 FDA reports)
SYRINGE ISSUE ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THOUGHT BROADCASTING ( 2 FDA reports)
THROAT LESION ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYROID CANCER STAGE II ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 2 FDA reports)
TOURETTE'S DISORDER ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT PSYCHOSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRICUSPID VALVE DISEASE ( 2 FDA reports)
TRIGEMINAL NERVE DISORDER ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TYPE II HYPERSENSITIVITY ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL HAEMORRHAGE ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
URINE KETONE BODY ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
UROGENITAL DISORDER ( 2 FDA reports)
UROGRAM ABNORMAL ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
UTEROVAGINAL PROLAPSE ( 2 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 2 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL CANCER METASTATIC ( 2 FDA reports)
VAGINAL EXFOLIATION ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL OEDEMA ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VITAMIN B2 INCREASED ( 2 FDA reports)
VITAMIN B6 DECREASED ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLUME BLOOD INCREASED ( 2 FDA reports)
VULVOVAGINITIS ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHITE CLOT SYNDROME ( 2 FDA reports)
WOUND CLOSURE ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
PARKINSONIAN CRISIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MUSCLES INADEQUATE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIANAL ERYTHEMA ( 1 FDA reports)
PERICARDIAL CYST ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY HYPOPLASIA ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATYBASIA ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POROKERATOSIS ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM HYPOPITUITARISM ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESBYOESOPHAGUS ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOLOGICAL FACTOR AFFECTING MEDICAL CONDITION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PUDENDAL CANAL SYNDROME ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RABBIT SYNDROME ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION DYSPHAGIA ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL FISTULA REPAIR ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFUSAL OF EXAMINATION ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY PARALYSIS ( 1 FDA reports)
RESPIRATORY RATE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINAL ANOMALY CONGENITAL ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
REYE'S SYNDROME ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 1 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SENSITISATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC ENCEPHALOPATHY ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLE ARTHRITIS ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINA BIFIDA OCCULTA ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPLENIC INFECTION BACTERIAL ( 1 FDA reports)
SPONDYLITIC MYELOPATHY ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBSTANCE USE ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SYDENHAM'S CHOREA ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TERTIARY SYPHILIS ( 1 FDA reports)
TESTICULAR CANCER METASTATIC ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL MASS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC ULCER ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICHOTILLOMANIA ( 1 FDA reports)
TROPICAL ULCER ( 1 FDA reports)
TRUANCY ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
TYRAMINE REACTION ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER AIRWAY NECROSIS ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VAGINAL OPERATION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS STENOSIS ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VERBALLY ABUSED ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRAL TRACHEITIS ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVAL CANCER STAGE II ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABSCESS SWEAT GLAND ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALLOIMMUNISATION ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAL PAP SMEAR ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANAPLASTIC CHOROID PLEXUS PAPILLOMA ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANION GAP ABNORMAL ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APGAR SCORE ABNORMAL ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE PERSPIRATION ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATOPY ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOMATISM EPILEPTIC ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERASCITES ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BANKRUPTCY ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BETA 2 GLOBULIN ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BILE OUTPUT DECREASED ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLADDER CATHETER PERMANENT ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER SPHINCTER ATONY ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLINDNESS DAY ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE ( 1 FDA reports)
BLOOD CARBON MONOXIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD COUNT ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 1 FDA reports)
BLOOD CULTURE ( 1 FDA reports)
BLOOD GLUCAGON DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OSMOLARITY ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GIANT CELL TUMOUR ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BORRELIA BURGDORFERI SEROLOGY POSITIVE ( 1 FDA reports)
BOTULISM ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL INJURY ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATARACT DIABETIC ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATARACT TRAUMATIC ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE BRUISE ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBRAL SALT-WASTING SYNDROME ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHEMICAL BURNS OF EYE ( 1 FDA reports)
CHEST WALL MASS ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHONDROLYSIS ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOACAL EXSTROPHY ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLORECTAL CANCER STAGE IV ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL FLOPPY INFANT ( 1 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 1 FDA reports)
CONGENITAL INFECTION ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL STRIAE ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF PROTEIN DECREASED ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYP2D6 POLYMORPHISM ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOREDUCTIVE SURGERY ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIVERTICULITIS MECKEL'S ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG HALF-LIFE REDUCED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
EAR CANAL STENOSIS ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELBOW OPERATION ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMPYEMA DRAINAGE ( 1 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 1 FDA reports)
ENCEPHALITIS PROTOZOAL ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
ENTEROBIASIS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EXCESSIVE OCULAR CONVERGENCE ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE LABOUR ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL DYSFUNCTION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL NERVE INJURY ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN ABNORMAL ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
FUNNEL CHEST ACQUIRED ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC LAVAGE ( 1 FDA reports)
GASTRIC OCCULT BLOOD POSITIVE ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOCELLULAR FOAMY CELL SYNDROME ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HEREDITARY OPTIC ATROPHY ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIPPUS ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE LYMPHOCYTE PREDOMINANCE TYPE STAGE UNSPECIFIED ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HUMAN HERPESVIRUS 7 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE CALCIFICATION ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLAMMATION OF LACRIMAL PASSAGE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE DISCOMFORT ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE ECZEMA ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL MALROTATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
INTRANEURAL CYST ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
K-RAS GENE MUTATION ( 1 FDA reports)
KARNOFSKY SCALE WORSENED ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KERATOSIS OBTURANS ( 1 FDA reports)
KIDNEY DUPLEX ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LACTOBACILLUS TEST POSITIVE ( 1 FDA reports)
LAGOPHTHALMOS ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARYNGEAL DISCOMFORT ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHADENITIS VIRAL ( 1 FDA reports)
LYMPHOCYTE COUNT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 1 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDIASTINAL ABSCESS ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS LEPTOSPIRAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENOPAUSAL DEPRESSION ( 1 FDA reports)
MENSTRUATION NORMAL ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MOUTH CYST ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL NECROSIS ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MURDER ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOCARDITIS INFECTIOUS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NAIL ATROPHY ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TACHYCARDIA ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 1 FDA reports)
NEUROMUSCULAR TOXICITY ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL COUNT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ABNORMAL ( 1 FDA reports)
NYMPHOMANIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOSCOPY ( 1 FDA reports)
OILY SKIN ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOGRYPHOSIS ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPHTHALMIC FLUID DRAINAGE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL POLYPECTOMY ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
ORNITHINE TRANSCARBAMOYLASE DEFICIENCY ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOARTHROPATHY ( 1 FDA reports)
OSTEOCALCIN ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOSALPINGITIS ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALATITIS ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PANCREATIC ENZYMES DECREASED ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)