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

ANXIETY ( 2991 FDA reports)
NAUSEA ( 2914 FDA reports)
PAIN ( 2724 FDA reports)
FATIGUE ( 2322 FDA reports)
DYSPNOEA ( 2247 FDA reports)
DEPRESSION ( 2036 FDA reports)
VOMITING ( 2005 FDA reports)
DIARRHOEA ( 1937 FDA reports)
HEADACHE ( 1837 FDA reports)
ASTHENIA ( 1807 FDA reports)
INSOMNIA ( 1684 FDA reports)
DIZZINESS ( 1604 FDA reports)
PYREXIA ( 1510 FDA reports)
BACK PAIN ( 1476 FDA reports)
ANAEMIA ( 1444 FDA reports)
CHEST PAIN ( 1399 FDA reports)
PNEUMONIA ( 1387 FDA reports)
ABDOMINAL PAIN ( 1350 FDA reports)
FALL ( 1349 FDA reports)
WEIGHT DECREASED ( 1330 FDA reports)
DEHYDRATION ( 1218 FDA reports)
ARTHRALGIA ( 1216 FDA reports)
OEDEMA PERIPHERAL ( 1212 FDA reports)
HYPERTENSION ( 1202 FDA reports)
DRUG INEFFECTIVE ( 1195 FDA reports)
PAIN IN EXTREMITY ( 1181 FDA reports)
INJURY ( 1171 FDA reports)
HYPOTENSION ( 1097 FDA reports)
CONFUSIONAL STATE ( 1077 FDA reports)
OSTEONECROSIS OF JAW ( 1061 FDA reports)
CONSTIPATION ( 1048 FDA reports)
BONE DISORDER ( 983 FDA reports)
DIABETES MELLITUS ( 936 FDA reports)
WEIGHT INCREASED ( 933 FDA reports)
CONVULSION ( 916 FDA reports)
COUGH ( 906 FDA reports)
EMOTIONAL DISTRESS ( 901 FDA reports)
HYPOAESTHESIA ( 884 FDA reports)
NEUROPATHY PERIPHERAL ( 884 FDA reports)
TREMOR ( 872 FDA reports)
URINARY TRACT INFECTION ( 863 FDA reports)
RASH ( 840 FDA reports)
PLEURAL EFFUSION ( 832 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 829 FDA reports)
DECREASED APPETITE ( 817 FDA reports)
SUICIDAL IDEATION ( 809 FDA reports)
DYSPHAGIA ( 796 FDA reports)
SOMNOLENCE ( 788 FDA reports)
OSTEOMYELITIS ( 777 FDA reports)
MALAISE ( 772 FDA reports)
DEATH ( 770 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 747 FDA reports)
RENAL FAILURE ( 745 FDA reports)
PAIN IN JAW ( 741 FDA reports)
PARAESTHESIA ( 721 FDA reports)
TYPE 2 DIABETES MELLITUS ( 718 FDA reports)
DEEP VEIN THROMBOSIS ( 712 FDA reports)
SPINAL OSTEOARTHRITIS ( 706 FDA reports)
BRONCHITIS ( 691 FDA reports)
GAIT DISTURBANCE ( 691 FDA reports)
FEELING ABNORMAL ( 679 FDA reports)
SEPSIS ( 676 FDA reports)
RENAL FAILURE ACUTE ( 675 FDA reports)
MUSCLE SPASMS ( 669 FDA reports)
CEREBROVASCULAR ACCIDENT ( 665 FDA reports)
TACHYCARDIA ( 663 FDA reports)
INFECTION ( 662 FDA reports)
ABDOMINAL PAIN UPPER ( 656 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 655 FDA reports)
AGITATION ( 651 FDA reports)
CELLULITIS ( 650 FDA reports)
THROMBOCYTOPENIA ( 640 FDA reports)
ATELECTASIS ( 621 FDA reports)
MENTAL STATUS CHANGES ( 595 FDA reports)
PALPITATIONS ( 593 FDA reports)
VISION BLURRED ( 593 FDA reports)
OSTEOARTHRITIS ( 592 FDA reports)
MYOCARDIAL INFARCTION ( 589 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 588 FDA reports)
SINUSITIS ( 576 FDA reports)
PULMONARY EMBOLISM ( 572 FDA reports)
HAEMOGLOBIN DECREASED ( 570 FDA reports)
LOSS OF CONSCIOUSNESS ( 561 FDA reports)
PANCYTOPENIA ( 558 FDA reports)
RESPIRATORY FAILURE ( 558 FDA reports)
CHILLS ( 555 FDA reports)
MYALGIA ( 553 FDA reports)
IMPAIRED HEALING ( 548 FDA reports)
MUSCULAR WEAKNESS ( 544 FDA reports)
FEBRILE NEUTROPENIA ( 534 FDA reports)
SWELLING ( 532 FDA reports)
SYNCOPE ( 531 FDA reports)
BLOOD GLUCOSE INCREASED ( 531 FDA reports)
OSTEONECROSIS ( 531 FDA reports)
TOOTH EXTRACTION ( 525 FDA reports)
CONDITION AGGRAVATED ( 522 FDA reports)
PRURITUS ( 519 FDA reports)
ANHEDONIA ( 514 FDA reports)
ATRIAL FIBRILLATION ( 507 FDA reports)
ERYTHEMA ( 501 FDA reports)
HYPERHIDROSIS ( 500 FDA reports)
OVERDOSE ( 497 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 494 FDA reports)
NEUTROPENIA ( 485 FDA reports)
CHEST DISCOMFORT ( 481 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 479 FDA reports)
NERVOUSNESS ( 479 FDA reports)
HALLUCINATION ( 475 FDA reports)
BONE PAIN ( 474 FDA reports)
LETHARGY ( 465 FDA reports)
HYPOKALAEMIA ( 462 FDA reports)
DYSPEPSIA ( 456 FDA reports)
DEFORMITY ( 455 FDA reports)
BLOOD PRESSURE INCREASED ( 448 FDA reports)
METASTASES TO BONE ( 448 FDA reports)
MEMORY IMPAIRMENT ( 446 FDA reports)
DENTAL CARIES ( 440 FDA reports)
NECK PAIN ( 432 FDA reports)
AMNESIA ( 430 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 422 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 419 FDA reports)
CONTUSION ( 418 FDA reports)
MITRAL VALVE INCOMPETENCE ( 409 FDA reports)
HEART RATE INCREASED ( 406 FDA reports)
HYPOXIA ( 404 FDA reports)
ARTHRITIS ( 401 FDA reports)
HYPONATRAEMIA ( 401 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 391 FDA reports)
PLATELET COUNT DECREASED ( 389 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 388 FDA reports)
HYPERGLYCAEMIA ( 386 FDA reports)
CORONARY ARTERY DISEASE ( 381 FDA reports)
OSTEOPENIA ( 380 FDA reports)
OEDEMA ( 378 FDA reports)
DRUG DEPENDENCE ( 376 FDA reports)
TOOTHACHE ( 375 FDA reports)
STRESS ( 373 FDA reports)
MUSCULOSKELETAL PAIN ( 373 FDA reports)
ABDOMINAL DISTENSION ( 372 FDA reports)
LYMPHADENOPATHY ( 370 FDA reports)
HYPERLIPIDAEMIA ( 369 FDA reports)
BALANCE DISORDER ( 367 FDA reports)
GASTRITIS ( 367 FDA reports)
HYPOPHAGIA ( 361 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 358 FDA reports)
SUICIDE ATTEMPT ( 358 FDA reports)
CARDIOMEGALY ( 357 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 356 FDA reports)
OSTEOPOROSIS ( 354 FDA reports)
HIATUS HERNIA ( 353 FDA reports)
BONE LESION ( 347 FDA reports)
CHOLELITHIASIS ( 340 FDA reports)
CARDIAC ARREST ( 338 FDA reports)
DECREASED INTEREST ( 335 FDA reports)
PANCREATITIS ( 335 FDA reports)
RIB FRACTURE ( 335 FDA reports)
CATARACT ( 333 FDA reports)
AGGRESSION ( 331 FDA reports)
DYSURIA ( 331 FDA reports)
MIGRAINE ( 329 FDA reports)
INFLAMMATION ( 326 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 326 FDA reports)
ALOPECIA ( 325 FDA reports)
MULTIPLE MYELOMA ( 324 FDA reports)
ABDOMINAL DISCOMFORT ( 322 FDA reports)
MUCOSAL INFLAMMATION ( 316 FDA reports)
SLEEP APNOEA SYNDROME ( 316 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 315 FDA reports)
HERPES ZOSTER ( 315 FDA reports)
HAEMATOCRIT DECREASED ( 314 FDA reports)
HAEMORRHOIDS ( 312 FDA reports)
DISEASE PROGRESSION ( 310 FDA reports)
PANIC ATTACK ( 308 FDA reports)
EAR PAIN ( 304 FDA reports)
TOOTH LOSS ( 304 FDA reports)
BLOOD CREATININE INCREASED ( 303 FDA reports)
LUNG NEOPLASM ( 303 FDA reports)
TOOTH DISORDER ( 300 FDA reports)
EXOSTOSIS ( 297 FDA reports)
PULMONARY OEDEMA ( 296 FDA reports)
ASTHMA ( 290 FDA reports)
PSYCHOTIC DISORDER ( 286 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 285 FDA reports)
HYPERSENSITIVITY ( 284 FDA reports)
PRIMARY SEQUESTRUM ( 283 FDA reports)
SINUS TACHYCARDIA ( 282 FDA reports)
DYSKINESIA ( 281 FDA reports)
DRY MOUTH ( 280 FDA reports)
NEOPLASM MALIGNANT ( 280 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 280 FDA reports)
IRRITABILITY ( 276 FDA reports)
RENAL FAILURE CHRONIC ( 275 FDA reports)
OROPHARYNGEAL PAIN ( 274 FDA reports)
DYSPNOEA EXERTIONAL ( 273 FDA reports)
OSTEOLYSIS ( 273 FDA reports)
ABNORMAL BEHAVIOUR ( 272 FDA reports)
COMPRESSION FRACTURE ( 272 FDA reports)
SLEEP DISORDER ( 271 FDA reports)
DYSARTHRIA ( 269 FDA reports)
POLLAKIURIA ( 269 FDA reports)
TOOTH ABSCESS ( 268 FDA reports)
PARANOIA ( 267 FDA reports)
DYSGEUSIA ( 264 FDA reports)
SWELLING FACE ( 264 FDA reports)
ORAL PAIN ( 263 FDA reports)
DIVERTICULUM ( 262 FDA reports)
MASTICATION DISORDER ( 261 FDA reports)
HEPATIC STEATOSIS ( 260 FDA reports)
DRUG INTERACTION ( 259 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 259 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 257 FDA reports)
FEAR ( 256 FDA reports)
HYPERCHOLESTEROLAEMIA ( 255 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 253 FDA reports)
STOMATITIS ( 253 FDA reports)
TREATMENT NONCOMPLIANCE ( 253 FDA reports)
SEPTIC SHOCK ( 250 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 250 FDA reports)
PURULENT DISCHARGE ( 249 FDA reports)
LUNG INFILTRATION ( 248 FDA reports)
BIPOLAR DISORDER ( 246 FDA reports)
URTICARIA ( 245 FDA reports)
RESPIRATORY DISTRESS ( 243 FDA reports)
SCAR ( 242 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 240 FDA reports)
EPISTAXIS ( 239 FDA reports)
MENTAL DISORDER ( 239 FDA reports)
JAW OPERATION ( 237 FDA reports)
MULTI-ORGAN FAILURE ( 237 FDA reports)
OBESITY ( 237 FDA reports)
CARDIO-RESPIRATORY ARREST ( 235 FDA reports)
DISORIENTATION ( 235 FDA reports)
CARDIAC DISORDER ( 234 FDA reports)
SPEECH DISORDER ( 234 FDA reports)
VERTIGO ( 233 FDA reports)
DISTURBANCE IN ATTENTION ( 233 FDA reports)
CRYING ( 232 FDA reports)
HOT FLUSH ( 232 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 232 FDA reports)
RENAL CYST ( 232 FDA reports)
BLOOD POTASSIUM DECREASED ( 228 FDA reports)
STAPHYLOCOCCAL INFECTION ( 227 FDA reports)
UNEVALUABLE EVENT ( 227 FDA reports)
UNRESPONSIVE TO STIMULI ( 224 FDA reports)
BLOOD PRESSURE DECREASED ( 224 FDA reports)
LEUKOPENIA ( 224 FDA reports)
DYSPHONIA ( 223 FDA reports)
HAEMATURIA ( 222 FDA reports)
ANOREXIA ( 221 FDA reports)
HYPOTHYROIDISM ( 221 FDA reports)
HAEMORRHAGE ( 220 FDA reports)
CARDIOMYOPATHY ( 218 FDA reports)
MOOD SWINGS ( 217 FDA reports)
OESOPHAGITIS ( 217 FDA reports)
RECTAL HAEMORRHAGE ( 217 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 216 FDA reports)
DISCOMFORT ( 215 FDA reports)
EMPHYSEMA ( 215 FDA reports)
NIGHT SWEATS ( 215 FDA reports)
ROAD TRAFFIC ACCIDENT ( 214 FDA reports)
SEDATION ( 213 FDA reports)
ANGINA PECTORIS ( 212 FDA reports)
ASCITES ( 212 FDA reports)
BRADYCARDIA ( 211 FDA reports)
DRUG DOSE OMISSION ( 211 FDA reports)
TOOTH FRACTURE ( 211 FDA reports)
FISTULA ( 210 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 210 FDA reports)
NEPHROLITHIASIS ( 210 FDA reports)
COMA ( 209 FDA reports)
DIABETIC NEUROPATHY ( 209 FDA reports)
THROMBOSIS ( 207 FDA reports)
URINARY INCONTINENCE ( 206 FDA reports)
ERECTILE DYSFUNCTION ( 205 FDA reports)
ANGER ( 204 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 204 FDA reports)
BURNING SENSATION ( 202 FDA reports)
LEUKOCYTOSIS ( 202 FDA reports)
WHEEZING ( 202 FDA reports)
BLOOD UREA INCREASED ( 200 FDA reports)
INFLUENZA LIKE ILLNESS ( 200 FDA reports)
SKIN LESION ( 199 FDA reports)
ARRHYTHMIA ( 198 FDA reports)
FLATULENCE ( 198 FDA reports)
FLUSHING ( 198 FDA reports)
MOUTH ULCERATION ( 198 FDA reports)
RENAL IMPAIRMENT ( 198 FDA reports)
FIBROMYALGIA ( 197 FDA reports)
OXYGEN SATURATION DECREASED ( 196 FDA reports)
BONE DEBRIDEMENT ( 195 FDA reports)
RESTLESSNESS ( 195 FDA reports)
ARTHROPATHY ( 194 FDA reports)
ECONOMIC PROBLEM ( 194 FDA reports)
HIP FRACTURE ( 194 FDA reports)
OFF LABEL USE ( 194 FDA reports)
PULMONARY HYPERTENSION ( 194 FDA reports)
TINNITUS ( 194 FDA reports)
SINUS DISORDER ( 193 FDA reports)
BURSITIS ( 193 FDA reports)
HYPERKALAEMIA ( 193 FDA reports)
PNEUMONIA ASPIRATION ( 193 FDA reports)
ARTERIOSCLEROSIS ( 192 FDA reports)
JOINT SWELLING ( 192 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 191 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 191 FDA reports)
LOOSE TOOTH ( 191 FDA reports)
PRODUCTIVE COUGH ( 191 FDA reports)
SPINAL COMPRESSION FRACTURE ( 190 FDA reports)
DELIRIUM ( 188 FDA reports)
JAW DISORDER ( 187 FDA reports)
JAW FRACTURE ( 185 FDA reports)
METASTASES TO SPINE ( 185 FDA reports)
BLOOD SODIUM DECREASED ( 183 FDA reports)
NASOPHARYNGITIS ( 183 FDA reports)
TENDERNESS ( 182 FDA reports)
VISUAL IMPAIRMENT ( 182 FDA reports)
MOBILITY DECREASED ( 181 FDA reports)
HAEMATOCHEZIA ( 180 FDA reports)
PERICARDIAL EFFUSION ( 179 FDA reports)
TARDIVE DYSKINESIA ( 179 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 179 FDA reports)
DEBRIDEMENT ( 178 FDA reports)
OSTEITIS ( 178 FDA reports)
PERIODONTAL DISEASE ( 177 FDA reports)
DIABETIC KETOACIDOSIS ( 174 FDA reports)
METASTASES TO LIVER ( 174 FDA reports)
BLOOD CALCIUM DECREASED ( 173 FDA reports)
HALLUCINATION, AUDITORY ( 172 FDA reports)
RESTLESS LEGS SYNDROME ( 171 FDA reports)
SURGERY ( 171 FDA reports)
MALNUTRITION ( 170 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 170 FDA reports)
DRUG TOXICITY ( 168 FDA reports)
FUNGAL INFECTION ( 168 FDA reports)
DRUG HYPERSENSITIVITY ( 167 FDA reports)
ORAL DISORDER ( 167 FDA reports)
EJECTION FRACTION DECREASED ( 165 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 165 FDA reports)
ONYCHOMYCOSIS ( 165 FDA reports)
OSTEOSCLEROSIS ( 165 FDA reports)
GINGIVITIS ( 164 FDA reports)
MEDICATION ERROR ( 164 FDA reports)
ABASIA ( 163 FDA reports)
CANDIDIASIS ( 163 FDA reports)
TOOTH INFECTION ( 163 FDA reports)
ABNORMAL DREAMS ( 162 FDA reports)
ACTINOMYCOSIS ( 162 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 162 FDA reports)
SPINAL COLUMN STENOSIS ( 161 FDA reports)
DISABILITY ( 160 FDA reports)
GRAND MAL CONVULSION ( 160 FDA reports)
HEAD INJURY ( 159 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 159 FDA reports)
FACIAL PAIN ( 158 FDA reports)
MAJOR DEPRESSION ( 158 FDA reports)
PHYSICAL DISABILITY ( 158 FDA reports)
CARPAL TUNNEL SYNDROME ( 157 FDA reports)
INCORRECT DOSE ADMINISTERED ( 157 FDA reports)
COLITIS ( 156 FDA reports)
HYPOCALCAEMIA ( 156 FDA reports)
PULMONARY CONGESTION ( 156 FDA reports)
EXPOSED BONE IN JAW ( 155 FDA reports)
LUMBAR SPINAL STENOSIS ( 155 FDA reports)
LUNG DISORDER ( 155 FDA reports)
METASTASES TO LUNG ( 154 FDA reports)
GASTROINTESTINAL DISORDER ( 153 FDA reports)
NASAL CONGESTION ( 153 FDA reports)
PATHOLOGICAL FRACTURE ( 153 FDA reports)
DEAFNESS ( 152 FDA reports)
DECUBITUS ULCER ( 152 FDA reports)
DEPRESSED MOOD ( 152 FDA reports)
GALLBLADDER DISORDER ( 152 FDA reports)
ORAL CANDIDIASIS ( 152 FDA reports)
TYPE 1 DIABETES MELLITUS ( 152 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 151 FDA reports)
DRUG EFFECT DECREASED ( 150 FDA reports)
HYPOGLYCAEMIA ( 150 FDA reports)
CEREBRAL INFARCTION ( 149 FDA reports)
HYPOVOLAEMIA ( 149 FDA reports)
NEURALGIA ( 149 FDA reports)
MUSCLE TWITCHING ( 148 FDA reports)
DIPLOPIA ( 147 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 147 FDA reports)
HEPATIC ENZYME INCREASED ( 147 FDA reports)
ORTHOSTATIC HYPOTENSION ( 147 FDA reports)
VISUAL ACUITY REDUCED ( 147 FDA reports)
HEPATIC LESION ( 146 FDA reports)
ROTATOR CUFF SYNDROME ( 144 FDA reports)
RHINITIS ALLERGIC ( 143 FDA reports)
JOINT STIFFNESS ( 143 FDA reports)
KYPHOSIS ( 143 FDA reports)
LIFE EXPECTANCY SHORTENED ( 142 FDA reports)
NIGHTMARE ( 142 FDA reports)
URINARY RETENTION ( 142 FDA reports)
APHASIA ( 141 FDA reports)
HEART RATE IRREGULAR ( 141 FDA reports)
FOOT FRACTURE ( 140 FDA reports)
SKIN EXFOLIATION ( 140 FDA reports)
TENDONITIS ( 140 FDA reports)
RHINORRHOEA ( 139 FDA reports)
SCOLIOSIS ( 139 FDA reports)
ILEUS ( 139 FDA reports)
PERIODONTITIS ( 139 FDA reports)
IRON DEFICIENCY ANAEMIA ( 138 FDA reports)
PNEUMOTHORAX ( 138 FDA reports)
BLOOD GLUCOSE DECREASED ( 137 FDA reports)
COGNITIVE DISORDER ( 137 FDA reports)
COORDINATION ABNORMAL ( 137 FDA reports)
GROIN PAIN ( 137 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 136 FDA reports)
GASTROENTERITIS ( 136 FDA reports)
INTESTINAL OBSTRUCTION ( 135 FDA reports)
ORAL CAVITY FISTULA ( 135 FDA reports)
DIVERTICULUM INTESTINAL ( 134 FDA reports)
EMOTIONAL DISORDER ( 134 FDA reports)
HAEMATOMA ( 134 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 134 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 134 FDA reports)
NERVOUS SYSTEM DISORDER ( 134 FDA reports)
SOFT TISSUE DISORDER ( 134 FDA reports)
STEM CELL TRANSPLANT ( 134 FDA reports)
BACTERIAL INFECTION ( 133 FDA reports)
BLOOD ALBUMIN DECREASED ( 133 FDA reports)
CYSTITIS ( 133 FDA reports)
DEMENTIA ( 133 FDA reports)
METABOLIC ACIDOSIS ( 133 FDA reports)
PRODUCT QUALITY ISSUE ( 133 FDA reports)
EATING DISORDER ( 132 FDA reports)
INJECTION SITE PAIN ( 132 FDA reports)
MANIA ( 132 FDA reports)
MUSCLE STRAIN ( 132 FDA reports)
INFLUENZA ( 131 FDA reports)
LACERATION ( 131 FDA reports)
BLOOD BILIRUBIN INCREASED ( 130 FDA reports)
CARDIAC MURMUR ( 130 FDA reports)
COLONIC POLYP ( 130 FDA reports)
FIBROSIS ( 130 FDA reports)
ENCEPHALOPATHY ( 129 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 129 FDA reports)
NEOPLASM PROGRESSION ( 129 FDA reports)
ACUTE RESPIRATORY FAILURE ( 128 FDA reports)
DELUSION ( 128 FDA reports)
DIVERTICULITIS ( 128 FDA reports)
FLANK PAIN ( 128 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 128 FDA reports)
OTITIS MEDIA ( 128 FDA reports)
DEVICE RELATED INFECTION ( 127 FDA reports)
HEPATIC CYST ( 127 FDA reports)
MASS ( 127 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 127 FDA reports)
ABSCESS ( 126 FDA reports)
ADVERSE DRUG REACTION ( 126 FDA reports)
CEREBRAL ISCHAEMIA ( 126 FDA reports)
PANCREATITIS ACUTE ( 126 FDA reports)
PHARYNGITIS ( 126 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 125 FDA reports)
ULCER ( 125 FDA reports)
SKIN DISORDER ( 124 FDA reports)
FLUID OVERLOAD ( 124 FDA reports)
AORTIC VALVE INCOMPETENCE ( 123 FDA reports)
DRY SKIN ( 123 FDA reports)
FEELING HOT ( 123 FDA reports)
CHRONIC SINUSITIS ( 122 FDA reports)
GINGIVAL BLEEDING ( 122 FDA reports)
HYPOMAGNESAEMIA ( 122 FDA reports)
INTERSTITIAL LUNG DISEASE ( 122 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 121 FDA reports)
MULTIPLE INJURIES ( 121 FDA reports)
PARAESTHESIA ORAL ( 121 FDA reports)
THINKING ABNORMAL ( 121 FDA reports)
VENTRICULAR TACHYCARDIA ( 121 FDA reports)
WITHDRAWAL SYNDROME ( 121 FDA reports)
COAGULOPATHY ( 120 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 120 FDA reports)
NOCTURIA ( 120 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 119 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 119 FDA reports)
HAEMOPTYSIS ( 119 FDA reports)
HALLUCINATION, VISUAL ( 119 FDA reports)
HYPOAESTHESIA ORAL ( 119 FDA reports)
ENDODONTIC PROCEDURE ( 118 FDA reports)
BODY TEMPERATURE INCREASED ( 117 FDA reports)
GASTRIC ULCER ( 117 FDA reports)
OVARIAN CYST ( 117 FDA reports)
VENTRICULAR HYPERTROPHY ( 117 FDA reports)
ACCIDENTAL OVERDOSE ( 116 FDA reports)
BREAST CANCER ( 116 FDA reports)
CHOLECYSTITIS ( 116 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 116 FDA reports)
INFUSION RELATED REACTION ( 116 FDA reports)
RESPIRATORY ARREST ( 116 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 115 FDA reports)
ORAL INFECTION ( 115 FDA reports)
POST PROCEDURAL COMPLICATION ( 115 FDA reports)
RADICULOPATHY ( 115 FDA reports)
RASH ERYTHEMATOUS ( 115 FDA reports)
SKIN ULCER ( 115 FDA reports)
VAGINAL HAEMORRHAGE ( 115 FDA reports)
BACTERAEMIA ( 114 FDA reports)
CERVICAL SPINAL STENOSIS ( 113 FDA reports)
HYPERSOMNIA ( 113 FDA reports)
SPLENOMEGALY ( 113 FDA reports)
ASPIRATION ( 112 FDA reports)
CARDIAC FAILURE ( 112 FDA reports)
CEREBRAL ATROPHY ( 112 FDA reports)
FAECAL INCONTINENCE ( 112 FDA reports)
FAILURE TO THRIVE ( 112 FDA reports)
LIBIDO DECREASED ( 112 FDA reports)
PNEUMONITIS ( 112 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 111 FDA reports)
PLASMACYTOSIS ( 111 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 111 FDA reports)
COMPLETED SUICIDE ( 110 FDA reports)
CONJUNCTIVITIS ( 110 FDA reports)
EYE PAIN ( 110 FDA reports)
GINGIVAL PAIN ( 110 FDA reports)
HEPATOMEGALY ( 110 FDA reports)
HYPERCALCAEMIA ( 110 FDA reports)
ILL-DEFINED DISORDER ( 110 FDA reports)
CROHN'S DISEASE ( 109 FDA reports)
DENTAL OPERATION ( 109 FDA reports)
PLEURAL FIBROSIS ( 109 FDA reports)
RASH PRURITIC ( 109 FDA reports)
SKIN DISCOLOURATION ( 109 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 109 FDA reports)
VIRAL INFECTION ( 108 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 108 FDA reports)
BONE DENSITY DECREASED ( 108 FDA reports)
LEFT ATRIAL DILATATION ( 108 FDA reports)
DRY EYE ( 107 FDA reports)
FEMUR FRACTURE ( 107 FDA reports)
NEUTROPHIL COUNT DECREASED ( 107 FDA reports)
RHINITIS ( 107 FDA reports)
DRUG ABUSE ( 105 FDA reports)
HEART RATE DECREASED ( 105 FDA reports)
INTENTIONAL OVERDOSE ( 105 FDA reports)
PLEURITIC PAIN ( 105 FDA reports)
HEPATIC FAILURE ( 104 FDA reports)
RENAL INJURY ( 103 FDA reports)
RHEUMATOID ARTHRITIS ( 103 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 102 FDA reports)
BONE LOSS ( 102 FDA reports)
HAEMATEMESIS ( 102 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 102 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 102 FDA reports)
EXCORIATION ( 101 FDA reports)
PRESYNCOPE ( 101 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 100 FDA reports)
CEREBRAL HAEMORRHAGE ( 100 FDA reports)
DENTURE WEARER ( 100 FDA reports)
LIVER DISORDER ( 100 FDA reports)
PALLOR ( 100 FDA reports)
TRISMUS ( 100 FDA reports)
WOUND DEHISCENCE ( 99 FDA reports)
FAECES DISCOLOURED ( 99 FDA reports)
HYPOACUSIS ( 99 FDA reports)
JOINT EFFUSION ( 99 FDA reports)
LACRIMATION INCREASED ( 99 FDA reports)
PROTHROMBIN TIME PROLONGED ( 99 FDA reports)
RASH MACULAR ( 99 FDA reports)
INTENTIONAL DRUG MISUSE ( 97 FDA reports)
RHABDOMYOLYSIS ( 97 FDA reports)
UTERINE LEIOMYOMA ( 97 FDA reports)
SINUS CONGESTION ( 96 FDA reports)
GINGIVAL DISORDER ( 96 FDA reports)
HOSPITALISATION ( 96 FDA reports)
JOINT INJURY ( 96 FDA reports)
DRUG ABUSER ( 95 FDA reports)
MENTAL IMPAIRMENT ( 95 FDA reports)
AORTIC ANEURYSM ( 94 FDA reports)
PHARYNGEAL OEDEMA ( 94 FDA reports)
POOR QUALITY SLEEP ( 94 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 94 FDA reports)
RASH GENERALISED ( 94 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 94 FDA reports)
ADVERSE EVENT ( 93 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 93 FDA reports)
FACET JOINT SYNDROME ( 93 FDA reports)
LOBAR PNEUMONIA ( 93 FDA reports)
MIDDLE INSOMNIA ( 93 FDA reports)
ORAL HERPES ( 93 FDA reports)
SINUS BRADYCARDIA ( 93 FDA reports)
ATAXIA ( 92 FDA reports)
CYST ( 92 FDA reports)
DERMATITIS ( 92 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 92 FDA reports)
CYANOSIS ( 91 FDA reports)
DYSTONIA ( 91 FDA reports)
FLUID RETENTION ( 91 FDA reports)
GASTRIC DISORDER ( 91 FDA reports)
HOMICIDAL IDEATION ( 91 FDA reports)
THROAT TIGHTNESS ( 91 FDA reports)
VASCULITIS ( 91 FDA reports)
FEELING COLD ( 90 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 89 FDA reports)
CHOLECYSTITIS CHRONIC ( 89 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 89 FDA reports)
FEELING JITTERY ( 89 FDA reports)
RENAL DISORDER ( 89 FDA reports)
ABDOMINAL HERNIA ( 88 FDA reports)
ABSCESS JAW ( 88 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 88 FDA reports)
HEMIPARESIS ( 88 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 88 FDA reports)
INCONTINENCE ( 88 FDA reports)
JAUNDICE ( 88 FDA reports)
MICTURITION URGENCY ( 88 FDA reports)
SEQUESTRECTOMY ( 88 FDA reports)
THYROID NEOPLASM ( 88 FDA reports)
SKIN INDURATION ( 87 FDA reports)
APATHY ( 87 FDA reports)
DENTAL FISTULA ( 87 FDA reports)
MUSCLE RIGIDITY ( 87 FDA reports)
MYELODYSPLASTIC SYNDROME ( 87 FDA reports)
AZOTAEMIA ( 86 FDA reports)
BLINDNESS ( 86 FDA reports)
GINGIVAL SWELLING ( 86 FDA reports)
IMPAIRED WORK ABILITY ( 86 FDA reports)
IRRITABLE BOWEL SYNDROME ( 86 FDA reports)
MOVEMENT DISORDER ( 86 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 86 FDA reports)
VIITH NERVE PARALYSIS ( 86 FDA reports)
MYOCARDIAL ISCHAEMIA ( 85 FDA reports)
BLISTER ( 84 FDA reports)
ECCHYMOSIS ( 84 FDA reports)
OPEN WOUND ( 84 FDA reports)
PHLEBITIS ( 84 FDA reports)
POLYURIA ( 84 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 83 FDA reports)
ANGINA UNSTABLE ( 83 FDA reports)
CAROTID ARTERY STENOSIS ( 83 FDA reports)
HYPERPLASIA ( 83 FDA reports)
PLATELET COUNT INCREASED ( 83 FDA reports)
SCIATICA ( 83 FDA reports)
SCHIZOPHRENIA ( 82 FDA reports)
SUBCUTANEOUS ABSCESS ( 82 FDA reports)
BREAST CANCER METASTATIC ( 82 FDA reports)
CATARACT OPERATION ( 82 FDA reports)
DRUG INTOLERANCE ( 82 FDA reports)
HYDRONEPHROSIS ( 82 FDA reports)
HYPOPHOSPHATAEMIA ( 82 FDA reports)
JOINT SPRAIN ( 82 FDA reports)
ANGIOPATHY ( 81 FDA reports)
ELECTROLYTE IMBALANCE ( 81 FDA reports)
HEPATITIS ( 81 FDA reports)
LIMB INJURY ( 81 FDA reports)
ORAL DISCOMFORT ( 81 FDA reports)
PULMONARY FIBROSIS ( 81 FDA reports)
SKIN FIBROSIS ( 81 FDA reports)
SKIN TIGHTNESS ( 81 FDA reports)
TONGUE ULCERATION ( 80 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 80 FDA reports)
BONE EROSION ( 80 FDA reports)
ODYNOPHAGIA ( 80 FDA reports)
ORAL INTAKE REDUCED ( 80 FDA reports)
RETCHING ( 80 FDA reports)
AFFECTIVE DISORDER ( 79 FDA reports)
DYSLIPIDAEMIA ( 79 FDA reports)
MULTIPLE SCLEROSIS ( 79 FDA reports)
PELVIC PAIN ( 79 FDA reports)
PROTEINURIA ( 79 FDA reports)
ABDOMINAL PAIN LOWER ( 78 FDA reports)
BEDRIDDEN ( 78 FDA reports)
INJECTION SITE ERYTHEMA ( 78 FDA reports)
LUNG NEOPLASM MALIGNANT ( 78 FDA reports)
MOOD ALTERED ( 78 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 78 FDA reports)
ANAPHYLACTIC REACTION ( 77 FDA reports)
BLOOD MAGNESIUM DECREASED ( 77 FDA reports)
BLOOD POTASSIUM INCREASED ( 77 FDA reports)
DYSSTASIA ( 77 FDA reports)
FACIAL PALSY ( 77 FDA reports)
GINGIVAL ULCERATION ( 77 FDA reports)
PLASMACYTOMA ( 77 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 77 FDA reports)
RESPIRATORY RATE INCREASED ( 77 FDA reports)
HYPERKERATOSIS ( 76 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 76 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 76 FDA reports)
MUSCLE TIGHTNESS ( 76 FDA reports)
SKIN HYPERTROPHY ( 76 FDA reports)
SPONDYLOLISTHESIS ( 76 FDA reports)
SQUAMOUS CELL CARCINOMA ( 76 FDA reports)
SENSORY DISTURBANCE ( 75 FDA reports)
TACHYPNOEA ( 75 FDA reports)
ADRENAL INSUFFICIENCY ( 75 FDA reports)
OSTEORADIONECROSIS ( 75 FDA reports)
ACUTE CORONARY SYNDROME ( 74 FDA reports)
OEDEMA MOUTH ( 74 FDA reports)
SPINAL DISORDER ( 74 FDA reports)
THROAT IRRITATION ( 74 FDA reports)
WALKING AID USER ( 74 FDA reports)
BONE MARROW FAILURE ( 73 FDA reports)
EAR INFECTION ( 73 FDA reports)
GRANULOCYTOPENIA ( 73 FDA reports)
MENISCUS LESION ( 73 FDA reports)
ACNE ( 72 FDA reports)
BIPOLAR I DISORDER ( 72 FDA reports)
COLD SWEAT ( 72 FDA reports)
INCREASED APPETITE ( 72 FDA reports)
KLEBSIELLA INFECTION ( 72 FDA reports)
CAESAREAN SECTION ( 71 FDA reports)
CERVICAL DYSPLASIA ( 71 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 71 FDA reports)
CORONARY ARTERY OCCLUSION ( 71 FDA reports)
GINGIVAL INFECTION ( 71 FDA reports)
GLAUCOMA ( 71 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 71 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 71 FDA reports)
SWOLLEN TONGUE ( 71 FDA reports)
BONE MARROW TRANSPLANT ( 70 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 70 FDA reports)
COLITIS ULCERATIVE ( 70 FDA reports)
GOUT ( 70 FDA reports)
JOINT DISLOCATION ( 70 FDA reports)
LOCAL SWELLING ( 69 FDA reports)
MITRAL VALVE PROLAPSE ( 69 FDA reports)
PSORIASIS ( 69 FDA reports)
UMBILICAL HERNIA ( 69 FDA reports)
SEXUAL DYSFUNCTION ( 68 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 68 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 68 FDA reports)
CHOKING ( 68 FDA reports)
LOWER LIMB FRACTURE ( 68 FDA reports)
LYMPHOEDEMA ( 68 FDA reports)
AKATHISIA ( 67 FDA reports)
CIRCULATORY COLLAPSE ( 67 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 67 FDA reports)
FACE OEDEMA ( 67 FDA reports)
FRACTURE ( 67 FDA reports)
HEPATITIS C ( 67 FDA reports)
MULTIPLE DRUG OVERDOSE ( 67 FDA reports)
NO THERAPEUTIC RESPONSE ( 67 FDA reports)
NODULE ( 67 FDA reports)
PANIC DISORDER ( 67 FDA reports)
STEVENS-JOHNSON SYNDROME ( 67 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 67 FDA reports)
SKIN LACERATION ( 66 FDA reports)
UROSEPSIS ( 66 FDA reports)
VENTRICULAR HYPOKINESIA ( 66 FDA reports)
BONE NEOPLASM MALIGNANT ( 66 FDA reports)
DILATATION VENTRICULAR ( 66 FDA reports)
ECZEMA ( 66 FDA reports)
LACUNAR INFARCTION ( 66 FDA reports)
LIMB DISCOMFORT ( 66 FDA reports)
PARALYSIS ( 66 FDA reports)
PRURITUS GENERALISED ( 66 FDA reports)
PSYCHIATRIC SYMPTOM ( 66 FDA reports)
BLOOD CHLORIDE DECREASED ( 65 FDA reports)
DERMATITIS CONTACT ( 65 FDA reports)
EYE DISORDER ( 65 FDA reports)
GOITRE ( 65 FDA reports)
HODGKIN'S DISEASE ( 65 FDA reports)
ISCHAEMIA ( 65 FDA reports)
METASTATIC NEOPLASM ( 65 FDA reports)
MOUTH HAEMORRHAGE ( 65 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 65 FDA reports)
TROPONIN INCREASED ( 64 FDA reports)
BREAST PAIN ( 64 FDA reports)
CERUMEN IMPACTION ( 64 FDA reports)
CLOSTRIDIAL INFECTION ( 64 FDA reports)
ERUCTATION ( 64 FDA reports)
EYE IRRITATION ( 64 FDA reports)
LIGAMENT SPRAIN ( 64 FDA reports)
POLYNEUROPATHY ( 64 FDA reports)
PROCEDURAL PAIN ( 64 FDA reports)
RALES ( 64 FDA reports)
APNOEA ( 63 FDA reports)
BLINDNESS UNILATERAL ( 63 FDA reports)
BRUXISM ( 63 FDA reports)
CARDIOVASCULAR DISORDER ( 63 FDA reports)
HERPES SIMPLEX ( 63 FDA reports)
POLYDIPSIA ( 63 FDA reports)
POST HERPETIC NEURALGIA ( 63 FDA reports)
WOUND DRAINAGE ( 63 FDA reports)
SKIN HYPERPIGMENTATION ( 62 FDA reports)
SPINAL CORD COMPRESSION ( 62 FDA reports)
CACHEXIA ( 62 FDA reports)
CATHETER PLACEMENT ( 62 FDA reports)
DIASTOLIC DYSFUNCTION ( 62 FDA reports)
INTENTIONAL SELF-INJURY ( 62 FDA reports)
ANXIETY DISORDER ( 61 FDA reports)
DIABETIC NEPHROPATHY ( 61 FDA reports)
EXTRASYSTOLES ( 61 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 61 FDA reports)
GENERALISED OEDEMA ( 61 FDA reports)
LUNG INFECTION ( 61 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 61 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 61 FDA reports)
PROCTALGIA ( 61 FDA reports)
RESPIRATORY DEPRESSION ( 61 FDA reports)
RESPIRATORY DISORDER ( 61 FDA reports)
TENOSYNOVITIS ( 61 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 61 FDA reports)
VISUAL DISTURBANCE ( 61 FDA reports)
WHEELCHAIR USER ( 61 FDA reports)
SKIN PAPILLOMA ( 60 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 60 FDA reports)
CATHETER RELATED INFECTION ( 60 FDA reports)
DRUG SCREEN POSITIVE ( 60 FDA reports)
EROSIVE OESOPHAGITIS ( 60 FDA reports)
MELAENA ( 60 FDA reports)
PAIN OF SKIN ( 60 FDA reports)
AGRANULOCYTOSIS ( 59 FDA reports)
ATRIAL FLUTTER ( 59 FDA reports)
BASAL CELL CARCINOMA ( 59 FDA reports)
BONE OPERATION ( 59 FDA reports)
BREAST MASS ( 59 FDA reports)
CARDIOGENIC SHOCK ( 59 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 59 FDA reports)
GASTRITIS EROSIVE ( 59 FDA reports)
PEPTIC ULCER ( 59 FDA reports)
PETECHIAE ( 59 FDA reports)
RHONCHI ( 59 FDA reports)
SNORING ( 59 FDA reports)
SYNOVIAL CYST ( 59 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 58 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 58 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 58 FDA reports)
HUMERUS FRACTURE ( 58 FDA reports)
MYOSITIS ( 58 FDA reports)
PHOTOPHOBIA ( 58 FDA reports)
ACUTE SINUSITIS ( 57 FDA reports)
DIFFICULTY IN WALKING ( 57 FDA reports)
LOCALISED INFECTION ( 57 FDA reports)
RADICULAR PAIN ( 57 FDA reports)
VENTRICULAR DYSFUNCTION ( 57 FDA reports)
STOMACH DISCOMFORT ( 56 FDA reports)
VAGINAL INFECTION ( 56 FDA reports)
ACTINIC KERATOSIS ( 56 FDA reports)
ANKLE FRACTURE ( 56 FDA reports)
BLOOD CULTURE POSITIVE ( 56 FDA reports)
DILATATION ATRIAL ( 56 FDA reports)
DYSPHEMIA ( 56 FDA reports)
HAEMODIALYSIS ( 56 FDA reports)
HORDEOLUM ( 56 FDA reports)
RENAL TUBULAR NECROSIS ( 56 FDA reports)
CATHETERISATION CARDIAC ( 55 FDA reports)
DIABETIC RETINOPATHY ( 55 FDA reports)
DIALYSIS ( 55 FDA reports)
DUODENITIS ( 55 FDA reports)
HEARING IMPAIRED ( 55 FDA reports)
INADEQUATE ANALGESIA ( 55 FDA reports)
METASTASES TO LYMPH NODES ( 55 FDA reports)
RASH MACULO-PAPULAR ( 55 FDA reports)
SKIN BURNING SENSATION ( 55 FDA reports)
THROMBOSIS IN DEVICE ( 55 FDA reports)
VENOUS INSUFFICIENCY ( 55 FDA reports)
SARCOIDOSIS ( 54 FDA reports)
BLADDER DISORDER ( 54 FDA reports)
BLOOD CALCIUM INCREASED ( 54 FDA reports)
BLOOD URINE PRESENT ( 54 FDA reports)
BONE FRAGMENTATION ( 54 FDA reports)
CHROMATURIA ( 54 FDA reports)
COSTOCHONDRITIS ( 54 FDA reports)
DERMAL CYST ( 54 FDA reports)
DROOLING ( 54 FDA reports)
EDENTULOUS ( 54 FDA reports)
EYELID PTOSIS ( 54 FDA reports)
FOOT DEFORMITY ( 54 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 54 FDA reports)
NECROSIS ( 54 FDA reports)
OTITIS EXTERNA ( 54 FDA reports)
PERSONALITY CHANGE ( 54 FDA reports)
PLEURISY ( 54 FDA reports)
APPENDICITIS ( 53 FDA reports)
ATRIAL SEPTAL DEFECT ( 53 FDA reports)
BREATH ODOUR ( 53 FDA reports)
DISEASE RECURRENCE ( 53 FDA reports)
EYE SWELLING ( 53 FDA reports)
GASTROENTERITIS VIRAL ( 53 FDA reports)
HYPOKINESIA ( 53 FDA reports)
IMPULSIVE BEHAVIOUR ( 53 FDA reports)
INJECTION SITE REACTION ( 53 FDA reports)
MYOCLONUS ( 53 FDA reports)
NECK INJURY ( 53 FDA reports)
PROSTATE CANCER ( 53 FDA reports)
SPUTUM DISCOLOURED ( 53 FDA reports)
TRANSAMINASES INCREASED ( 53 FDA reports)
THIRST ( 52 FDA reports)
THYROID DISORDER ( 52 FDA reports)
VARICOSE VEIN ( 52 FDA reports)
VENTRICULAR FIBRILLATION ( 52 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 52 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 52 FDA reports)
BRONCHOSPASM ( 52 FDA reports)
ENDOTRACHEAL INTUBATION ( 52 FDA reports)
ENTEROCOCCAL INFECTION ( 52 FDA reports)
HAEMANGIOMA ( 52 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 52 FDA reports)
INITIAL INSOMNIA ( 52 FDA reports)
LYMPHOMA ( 52 FDA reports)
NEOPLASM ( 52 FDA reports)
ORAL SURGERY ( 52 FDA reports)
RENAL PAIN ( 52 FDA reports)
BRAIN OEDEMA ( 51 FDA reports)
GINGIVAL RECESSION ( 51 FDA reports)
HAND FRACTURE ( 51 FDA reports)
HEART VALVE INCOMPETENCE ( 51 FDA reports)
HILAR LYMPHADENOPATHY ( 51 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 51 FDA reports)
LARYNGITIS ( 51 FDA reports)
PANCREATITIS CHRONIC ( 51 FDA reports)
PSEUDOMONAS INFECTION ( 51 FDA reports)
SPINAL FRACTURE ( 51 FDA reports)
VULVOVAGINAL DRYNESS ( 51 FDA reports)
URINE OUTPUT DECREASED ( 50 FDA reports)
VITREOUS FLOATERS ( 50 FDA reports)
BACK DISORDER ( 50 FDA reports)
EAR CONGESTION ( 50 FDA reports)
EPICONDYLITIS ( 50 FDA reports)
FISTULA DISCHARGE ( 50 FDA reports)
HYPERTHYROIDISM ( 50 FDA reports)
HYPERVENTILATION ( 50 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 50 FDA reports)
INCREASED TENDENCY TO BRUISE ( 50 FDA reports)
LUNG CONSOLIDATION ( 50 FDA reports)
MUSCLE ATROPHY ( 50 FDA reports)
MUSCULOSKELETAL DISORDER ( 50 FDA reports)
NEURITIS ( 50 FDA reports)
NON-CARDIAC CHEST PAIN ( 50 FDA reports)
ACUTE PULMONARY OEDEMA ( 49 FDA reports)
BACK INJURY ( 49 FDA reports)
COLITIS ISCHAEMIC ( 49 FDA reports)
DIABETIC COMA ( 49 FDA reports)
MACULAR DEGENERATION ( 49 FDA reports)
NEUROGENIC BLADDER ( 49 FDA reports)
NEUROPATHY ( 49 FDA reports)
VAGINAL DISCHARGE ( 49 FDA reports)
WOUND INFECTION ( 49 FDA reports)
X-RAY ABNORMAL ( 48 FDA reports)
ADJUSTMENT DISORDER ( 48 FDA reports)
ANGIOEDEMA ( 48 FDA reports)
AORTIC CALCIFICATION ( 48 FDA reports)
APHAGIA ( 48 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 48 FDA reports)
CHOLECYSTECTOMY ( 48 FDA reports)
FRACTURED SACRUM ( 48 FDA reports)
GYNAECOMASTIA ( 48 FDA reports)
LEUKOENCEPHALOPATHY ( 48 FDA reports)
NEUTROPHIL COUNT INCREASED ( 48 FDA reports)
OCCULT BLOOD POSITIVE ( 48 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 48 FDA reports)
PROSTATOMEGALY ( 48 FDA reports)
AFFECT LABILITY ( 47 FDA reports)
DEAFNESS NEUROSENSORY ( 47 FDA reports)
DRUG ADMINISTRATION ERROR ( 47 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 47 FDA reports)
HEMIPLEGIA ( 47 FDA reports)
INCOHERENT ( 47 FDA reports)
LIP SWELLING ( 47 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 47 FDA reports)
MELANOCYTIC NAEVUS ( 47 FDA reports)
PERICARDITIS ( 47 FDA reports)
QUALITY OF LIFE DECREASED ( 47 FDA reports)
RADIOTHERAPY ( 47 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 47 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 47 FDA reports)
THROMBOCYTOSIS ( 47 FDA reports)
SKIN CANCER ( 46 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 46 FDA reports)
ACCIDENT ( 46 FDA reports)
AORTIC STENOSIS ( 46 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 46 FDA reports)
BREAST CANCER RECURRENT ( 46 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 46 FDA reports)
MYOPATHY ( 46 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 45 FDA reports)
CHOLECYSTITIS ACUTE ( 45 FDA reports)
DRUG TOLERANCE ( 45 FDA reports)
ENTERITIS ( 45 FDA reports)
HERPES VIRUS INFECTION ( 45 FDA reports)
HYPERPARATHYROIDISM ( 45 FDA reports)
HYPOAESTHESIA FACIAL ( 45 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 45 FDA reports)
JUGULAR VEIN THROMBOSIS ( 45 FDA reports)
MECHANICAL VENTILATION ( 45 FDA reports)
METABOLIC DISORDER ( 45 FDA reports)
PERIPHERAL ISCHAEMIA ( 45 FDA reports)
SKELETAL INJURY ( 45 FDA reports)
SKIN NEOPLASM EXCISION ( 45 FDA reports)
THROMBOPHLEBITIS ( 45 FDA reports)
STREPTOCOCCAL INFECTION ( 44 FDA reports)
THERAPY NON-RESPONDER ( 44 FDA reports)
WRIST FRACTURE ( 44 FDA reports)
BONE SWELLING ( 44 FDA reports)
EAR DISCOMFORT ( 44 FDA reports)
EPILEPSY ( 44 FDA reports)
HEPATIC CIRRHOSIS ( 44 FDA reports)
HYPERPHAGIA ( 44 FDA reports)
LUNG HYPERINFLATION ( 44 FDA reports)
PERIPHERAL COLDNESS ( 44 FDA reports)
PRESCRIBED OVERDOSE ( 44 FDA reports)
PULSE ABSENT ( 44 FDA reports)
RADIATION INJURY ( 44 FDA reports)
ABDOMINAL ABSCESS ( 43 FDA reports)
BONE FORMATION INCREASED ( 43 FDA reports)
ENDOCARDITIS ( 43 FDA reports)
EOSINOPHIL COUNT INCREASED ( 43 FDA reports)
EYE PRURITUS ( 43 FDA reports)
IMPAIRED DRIVING ABILITY ( 43 FDA reports)
INTERMITTENT CLAUDICATION ( 43 FDA reports)
MENORRHAGIA ( 43 FDA reports)
NEPHROPATHY ( 43 FDA reports)
PELVIC FRACTURE ( 43 FDA reports)
PROTEIN TOTAL DECREASED ( 43 FDA reports)
REFLUX OESOPHAGITIS ( 43 FDA reports)
RESPIRATORY TRACT CONGESTION ( 43 FDA reports)
TENDON DISORDER ( 43 FDA reports)
TONGUE INJURY ( 43 FDA reports)
SCAB ( 42 FDA reports)
SHOCK ( 42 FDA reports)
SKIN PLAQUE ( 42 FDA reports)
STRESS FRACTURE ( 42 FDA reports)
WOUND ( 42 FDA reports)
BRAIN INJURY ( 42 FDA reports)
BREATH SOUNDS ABNORMAL ( 42 FDA reports)
BRONCHITIS ACUTE ( 42 FDA reports)
CORONARY ARTERY BYPASS ( 42 FDA reports)
DEPERSONALISATION ( 42 FDA reports)
FURUNCLE ( 42 FDA reports)
HYPOALBUMINAEMIA ( 42 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 42 FDA reports)
KIDNEY INFECTION ( 42 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 42 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 42 FDA reports)
PERSONALITY DISORDER ( 42 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 42 FDA reports)
BODY TEMPERATURE DECREASED ( 41 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 41 FDA reports)
CYSTITIS HAEMORRHAGIC ( 41 FDA reports)
CYSTOCELE ( 41 FDA reports)
DYSTHYMIC DISORDER ( 41 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 41 FDA reports)
EYELID OEDEMA ( 41 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 41 FDA reports)
LUMBAR RADICULOPATHY ( 41 FDA reports)
MARROW HYPERPLASIA ( 41 FDA reports)
MASTECTOMY ( 41 FDA reports)
PATHOLOGICAL GAMBLING ( 41 FDA reports)
PLANTAR FASCIITIS ( 41 FDA reports)
SUBSTANCE ABUSE ( 41 FDA reports)
TOOTH DEPOSIT ( 41 FDA reports)
UPPER LIMB FRACTURE ( 41 FDA reports)
SENSITIVITY OF TEETH ( 40 FDA reports)
SOMNAMBULISM ( 40 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 40 FDA reports)
ACCIDENT AT WORK ( 40 FDA reports)
BREAST CANCER FEMALE ( 40 FDA reports)
BREAST RECONSTRUCTION ( 40 FDA reports)
CHRONIC FATIGUE SYNDROME ( 40 FDA reports)
DENTAL CARE ( 40 FDA reports)
ESSENTIAL TREMOR ( 40 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 40 FDA reports)
GRAFT VERSUS HOST DISEASE ( 40 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 40 FDA reports)
INCISIONAL DRAINAGE ( 40 FDA reports)
INJECTION SITE HAEMORRHAGE ( 40 FDA reports)
JOINT CREPITATION ( 40 FDA reports)
MENINGITIS ( 40 FDA reports)
MUSCLE DISORDER ( 40 FDA reports)
ORTHOPNOEA ( 40 FDA reports)
PANIC REACTION ( 40 FDA reports)
PARKINSON'S DISEASE ( 40 FDA reports)
PERITONEAL DISORDER ( 40 FDA reports)
PERONEAL NERVE PALSY ( 40 FDA reports)
ABSCESS DRAINAGE ( 39 FDA reports)
CATHETER RELATED COMPLICATION ( 39 FDA reports)
CORONARY ARTERY STENOSIS ( 39 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 39 FDA reports)
GLOSSODYNIA ( 39 FDA reports)
HYPERBILIRUBINAEMIA ( 39 FDA reports)
HYPOMANIA ( 39 FDA reports)
INTRACRANIAL ANEURYSM ( 39 FDA reports)
LIPASE INCREASED ( 39 FDA reports)
NAIL DISORDER ( 39 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 39 FDA reports)
OVERWEIGHT ( 39 FDA reports)
POOR PERSONAL HYGIENE ( 39 FDA reports)
PULMONARY INFARCTION ( 39 FDA reports)
PYELONEPHRITIS ( 39 FDA reports)
SINUS HEADACHE ( 39 FDA reports)
TONGUE DISORDER ( 39 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 39 FDA reports)
SKIN IRRITATION ( 38 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 38 FDA reports)
TOOTH EROSION ( 38 FDA reports)
ABSCESS ORAL ( 38 FDA reports)
ACIDOSIS ( 38 FDA reports)
ADENOCARCINOMA ( 38 FDA reports)
AGORAPHOBIA ( 38 FDA reports)
AMENORRHOEA ( 38 FDA reports)
APPETITE DISORDER ( 38 FDA reports)
BARRETT'S OESOPHAGUS ( 38 FDA reports)
CAROTID ARTERY DISEASE ( 38 FDA reports)
CERVICOBRACHIAL SYNDROME ( 38 FDA reports)
CHEST X-RAY ABNORMAL ( 38 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 38 FDA reports)
EMPYEMA ( 38 FDA reports)
ESCHERICHIA INFECTION ( 38 FDA reports)
FAECALOMA ( 38 FDA reports)
FEELING OF DESPAIR ( 38 FDA reports)
FRACTURE NONUNION ( 38 FDA reports)
GUN SHOT WOUND ( 38 FDA reports)
HOSTILITY ( 38 FDA reports)
INGROWING NAIL ( 38 FDA reports)
OVARIAN CANCER ( 38 FDA reports)
PHOTOPSIA ( 38 FDA reports)
POLYP ( 38 FDA reports)
ALCOHOLISM ( 37 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 37 FDA reports)
APPENDICITIS PERFORATED ( 37 FDA reports)
BODY HEIGHT DECREASED ( 37 FDA reports)
BONE SCAN ABNORMAL ( 37 FDA reports)
CRANIAL NERVE DISORDER ( 37 FDA reports)
DEPENDENCE ( 37 FDA reports)
DRUG LEVEL INCREASED ( 37 FDA reports)
EMBOLISM ( 37 FDA reports)
EOSINOPHILIA ( 37 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 37 FDA reports)
GENERALISED ANXIETY DISORDER ( 37 FDA reports)
GINGIVAL OEDEMA ( 37 FDA reports)
HYPERAESTHESIA ( 37 FDA reports)
HYPERCOAGULATION ( 37 FDA reports)
LIGAMENT RUPTURE ( 37 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 37 FDA reports)
METABOLIC ENCEPHALOPATHY ( 37 FDA reports)
QRS AXIS ABNORMAL ( 37 FDA reports)
SENSORY LOSS ( 37 FDA reports)
URINARY HESITATION ( 37 FDA reports)
VERTEBROPLASTY ( 37 FDA reports)
SEBORRHOEIC KERATOSIS ( 36 FDA reports)
TIBIA FRACTURE ( 36 FDA reports)
ANEURYSM ( 36 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 36 FDA reports)
BILE DUCT STONE ( 36 FDA reports)
BREAST TENDERNESS ( 36 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 36 FDA reports)
DERMATITIS ACNEIFORM ( 36 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 36 FDA reports)
ENCEPHALOMALACIA ( 36 FDA reports)
FOREIGN BODY ( 36 FDA reports)
GASTRIC HAEMORRHAGE ( 36 FDA reports)
HICCUPS ( 36 FDA reports)
HIP ARTHROPLASTY ( 36 FDA reports)
INGUINAL HERNIA ( 36 FDA reports)
INJECTION SITE HAEMATOMA ( 36 FDA reports)
INTENTIONAL MISUSE ( 36 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 36 FDA reports)
LABORATORY TEST ABNORMAL ( 36 FDA reports)
NEPHROSCLEROSIS ( 36 FDA reports)
OSTEOMYELITIS CHRONIC ( 36 FDA reports)
PERITONITIS ( 36 FDA reports)
PROCEDURAL COMPLICATION ( 36 FDA reports)
RECTOCELE ( 36 FDA reports)
ADRENAL MASS ( 35 FDA reports)
ALCOHOL USE ( 35 FDA reports)
CANCER PAIN ( 35 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 35 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 35 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 35 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 35 FDA reports)
ENERGY INCREASED ( 35 FDA reports)
HYPOVENTILATION ( 35 FDA reports)
INTESTINAL ISCHAEMIA ( 35 FDA reports)
INTESTINAL PERFORATION ( 35 FDA reports)
MITRAL VALVE DISEASE ( 35 FDA reports)
MOTOR DYSFUNCTION ( 35 FDA reports)
OESOPHAGEAL ULCER ( 35 FDA reports)
PERFORMANCE STATUS DECREASED ( 35 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 35 FDA reports)
PURULENCE ( 35 FDA reports)
SYNOVITIS ( 35 FDA reports)
TENDON RUPTURE ( 35 FDA reports)
VARICES OESOPHAGEAL ( 35 FDA reports)
VITAMIN D DEFICIENCY ( 35 FDA reports)
SELF-INJURIOUS IDEATION ( 34 FDA reports)
SINUS ARRHYTHMIA ( 34 FDA reports)
SUBDURAL HAEMATOMA ( 34 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 34 FDA reports)
TACHYPHRENIA ( 34 FDA reports)
TEARFULNESS ( 34 FDA reports)
ADRENAL DISORDER ( 34 FDA reports)
CARDIAC ANEURYSM ( 34 FDA reports)
FIBULA FRACTURE ( 34 FDA reports)
HEPATIC NECROSIS ( 34 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 34 FDA reports)
OLIGURIA ( 34 FDA reports)
PROTEIN TOTAL INCREASED ( 34 FDA reports)
ALVEOLOPLASTY ( 33 FDA reports)
AORTIC VALVE SCLEROSIS ( 33 FDA reports)
ATROPHIC VULVOVAGINITIS ( 33 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 33 FDA reports)
COLON CANCER ( 33 FDA reports)
DISSOCIATION ( 33 FDA reports)
EUPHORIC MOOD ( 33 FDA reports)
FACIAL BONES FRACTURE ( 33 FDA reports)
HYPERTENSIVE HEART DISEASE ( 33 FDA reports)
LOGORRHOEA ( 33 FDA reports)
MENINGIOMA ( 33 FDA reports)
PANCREATIC CARCINOMA ( 33 FDA reports)
PRESBYOPIA ( 33 FDA reports)
SALIVARY HYPERSECRETION ( 33 FDA reports)
T-CELL LYMPHOMA ( 33 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 33 FDA reports)
SENSATION OF FOREIGN BODY ( 32 FDA reports)
STREPTOCOCCAL SEPSIS ( 32 FDA reports)
TOOTH REPAIR ( 32 FDA reports)
UMBILICAL CORD ABNORMALITY ( 32 FDA reports)
UTERINE POLYP ( 32 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 32 FDA reports)
AREFLEXIA ( 32 FDA reports)
ATROPHY ( 32 FDA reports)
BACTERIAL TEST POSITIVE ( 32 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 32 FDA reports)
BRAIN NEOPLASM ( 32 FDA reports)
CARDIAC VALVE DISEASE ( 32 FDA reports)
CATHETER REMOVAL ( 32 FDA reports)
DENTAL PLAQUE ( 32 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 32 FDA reports)
DIABETIC FOOT ( 32 FDA reports)
EYE HAEMORRHAGE ( 32 FDA reports)
FORMICATION ( 32 FDA reports)
GINGIVAL ERYTHEMA ( 32 FDA reports)
HYPERNATRAEMIA ( 32 FDA reports)
INJECTION SITE IRRITATION ( 32 FDA reports)
ISCHAEMIC STROKE ( 32 FDA reports)
MUSCLE CRAMP ( 32 FDA reports)
NECK MASS ( 32 FDA reports)
PAPILLOMA ( 32 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 32 FDA reports)
RAYNAUD'S PHENOMENON ( 32 FDA reports)
RECTAL POLYP ( 32 FDA reports)
ABDOMINAL TENDERNESS ( 31 FDA reports)
ABORTION SPONTANEOUS ( 31 FDA reports)
ADENOMA BENIGN ( 31 FDA reports)
ARTERIAL DISORDER ( 31 FDA reports)
BRONCHIECTASIS ( 31 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 31 FDA reports)
CONVERSION DISORDER ( 31 FDA reports)
CULTURE URINE POSITIVE ( 31 FDA reports)
DEVICE FAILURE ( 31 FDA reports)
EAR DISORDER ( 31 FDA reports)
FACIAL PARESIS ( 31 FDA reports)
GRANULOMA ( 31 FDA reports)
HAEMATOCRIT INCREASED ( 31 FDA reports)
IMMUNOSUPPRESSION ( 31 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 31 FDA reports)
LARGE INTESTINE PERFORATION ( 31 FDA reports)
NICOTINE DEPENDENCE ( 31 FDA reports)
PARKINSONISM ( 31 FDA reports)
PULMONARY MASS ( 31 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 31 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 31 FDA reports)
TENSION ( 31 FDA reports)
THYROID CYST ( 31 FDA reports)
VITAMIN B12 DEFICIENCY ( 31 FDA reports)
SERUM FERRITIN INCREASED ( 30 FDA reports)
BIOPSY ( 30 FDA reports)
CARDIAC FLUTTER ( 30 FDA reports)
CARDIAC TAMPONADE ( 30 FDA reports)
CLAUSTROPHOBIA ( 30 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 30 FDA reports)
DIAPHRAGMATIC HERNIA ( 30 FDA reports)
DYSTROPHIC CALCIFICATION ( 30 FDA reports)
ESSENTIAL HYPERTENSION ( 30 FDA reports)
HAEMOLYTIC ANAEMIA ( 30 FDA reports)
IMMUNODEFICIENCY ( 30 FDA reports)
IMPETIGO ( 30 FDA reports)
INJECTION SITE PRURITUS ( 30 FDA reports)
METABOLIC SYNDROME ( 30 FDA reports)
OCULAR HYPERAEMIA ( 30 FDA reports)
PARAPLEGIA ( 30 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 29 FDA reports)
APPLICATION SITE PRURITUS ( 29 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 29 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 29 FDA reports)
CORONARY ARTERY RESTENOSIS ( 29 FDA reports)
DYSAESTHESIA ( 29 FDA reports)
FLIGHT OF IDEAS ( 29 FDA reports)
GANGRENE ( 29 FDA reports)
INTRAOCULAR LENS IMPLANT ( 29 FDA reports)
KYPHOSCOLIOSIS ( 29 FDA reports)
LIPOMA ( 29 FDA reports)
LOCALISED OEDEMA ( 29 FDA reports)
MALIGNANT MELANOMA ( 29 FDA reports)
MONOCYTE COUNT INCREASED ( 29 FDA reports)
MYELOMA RECURRENCE ( 29 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 29 FDA reports)
POOR DENTAL CONDITION ( 29 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 29 FDA reports)
PURPURA ( 29 FDA reports)
SENSATION OF HEAVINESS ( 29 FDA reports)
SIALOADENITIS ( 29 FDA reports)
SINUS OPERATION ( 29 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 29 FDA reports)
THERMAL BURN ( 29 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 29 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 29 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 28 FDA reports)
SEBORRHOEIC DERMATITIS ( 28 FDA reports)
SINUS POLYP ( 28 FDA reports)
SPLENIC LESION ( 28 FDA reports)
STARING ( 28 FDA reports)
STUPOR ( 28 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 28 FDA reports)
TROPONIN I INCREASED ( 28 FDA reports)
UTERINE HAEMORRHAGE ( 28 FDA reports)
VOCAL CORD PARALYSIS ( 28 FDA reports)
ACUTE PRERENAL FAILURE ( 28 FDA reports)
ANOGENITAL WARTS ( 28 FDA reports)
BLEPHARITIS ( 28 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 28 FDA reports)
BLOOD PRESSURE ABNORMAL ( 28 FDA reports)
BONE TRIMMING ( 28 FDA reports)
DIABETIC COMPLICATION ( 28 FDA reports)
EMBOLIC STROKE ( 28 FDA reports)
EPIGASTRIC DISCOMFORT ( 28 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 28 FDA reports)
FIBROUS HISTIOCYTOMA ( 28 FDA reports)
FLUID INTAKE REDUCED ( 28 FDA reports)
HIP SURGERY ( 28 FDA reports)
HISTOPLASMOSIS ( 28 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 28 FDA reports)
HYPERTROPHY BREAST ( 28 FDA reports)
INCISION SITE COMPLICATION ( 28 FDA reports)
KETOACIDOSIS ( 28 FDA reports)
LYMPHADENECTOMY ( 28 FDA reports)
LYMPHOPENIA ( 28 FDA reports)
METASTASES TO SKIN ( 28 FDA reports)
OESOPHAGEAL DISORDER ( 28 FDA reports)
PAROSMIA ( 28 FDA reports)
PLACENTAL INSUFFICIENCY ( 28 FDA reports)
PRIMARY HYPOGONADISM ( 28 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 28 FDA reports)
ALCOHOL ABUSE ( 27 FDA reports)
APPENDICECTOMY ( 27 FDA reports)
APPLICATION SITE ERYTHEMA ( 27 FDA reports)
ARTHROSCOPY ( 27 FDA reports)
CATARACT NUCLEAR ( 27 FDA reports)
COMMUNICATION DISORDER ( 27 FDA reports)
COMPLEX PARTIAL SEIZURES ( 27 FDA reports)
CUTIS LAXA ( 27 FDA reports)
DECREASED ACTIVITY ( 27 FDA reports)
DROP ATTACKS ( 27 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 27 FDA reports)
GALLBLADDER POLYP ( 27 FDA reports)
GLOBULINS INCREASED ( 27 FDA reports)
GLOSSITIS ( 27 FDA reports)
ILEUS PARALYTIC ( 27 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 27 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 27 FDA reports)
OCULAR HYPERTENSION ( 27 FDA reports)
OESOPHAGITIS ULCERATIVE ( 27 FDA reports)
OSTEOMALACIA ( 27 FDA reports)
PALATAL DISORDER ( 27 FDA reports)
PANCREATIC ATROPHY ( 27 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 27 FDA reports)
PETIT MAL EPILEPSY ( 27 FDA reports)
REFLUX LARYNGITIS ( 27 FDA reports)
RESPIRATORY RATE DECREASED ( 27 FDA reports)
SACROILIITIS ( 27 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 27 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 27 FDA reports)
SYNCOPE VASOVAGAL ( 27 FDA reports)
TACHYARRHYTHMIA ( 27 FDA reports)
TOOTH IMPACTED ( 27 FDA reports)
TRANSFUSION ( 27 FDA reports)
URETERIC OBSTRUCTION ( 27 FDA reports)
URINARY TRACT DISORDER ( 27 FDA reports)
WEIGHT FLUCTUATION ( 27 FDA reports)
SKIN INFECTION ( 26 FDA reports)
SPINAL LAMINECTOMY ( 26 FDA reports)
THYROID CANCER ( 26 FDA reports)
UNDERDOSE ( 26 FDA reports)
ACCIDENT AT HOME ( 26 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 26 FDA reports)
ANURIA ( 26 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 26 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 26 FDA reports)
CARDIAC OPERATION ( 26 FDA reports)
CERVIX CARCINOMA ( 26 FDA reports)
CHORIOAMNIONITIS ( 26 FDA reports)
DIZZINESS POSTURAL ( 26 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 26 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 26 FDA reports)
EXOPHTHALMOS ( 26 FDA reports)
EXTRASKELETAL OSSIFICATION ( 26 FDA reports)
GASTRIC POLYPS ( 26 FDA reports)
GINGIVAL ABSCESS ( 26 FDA reports)
HAEMOLYSIS ( 26 FDA reports)
HEPATIC NEOPLASM ( 26 FDA reports)
HYDROCEPHALUS ( 26 FDA reports)
HYPERACUSIS ( 26 FDA reports)
HYPERCAPNIA ( 26 FDA reports)
INJECTION SITE RASH ( 26 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 26 FDA reports)
MENIERE'S DISEASE ( 26 FDA reports)
METASTASES TO SPLEEN ( 26 FDA reports)
METASTASIS ( 26 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 26 FDA reports)
OESOPHAGEAL PAIN ( 26 FDA reports)
PERIARTHRITIS ( 26 FDA reports)
PNEUMONIA FUNGAL ( 26 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 26 FDA reports)
PULMONARY HAEMORRHAGE ( 26 FDA reports)
RADIUS FRACTURE ( 26 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 26 FDA reports)
RESORPTION BONE INCREASED ( 26 FDA reports)
APLASIA PURE RED CELL ( 25 FDA reports)
BACTERIAL SEPSIS ( 25 FDA reports)
BRAIN SCAN ABNORMAL ( 25 FDA reports)
CAROTID BRUIT ( 25 FDA reports)
CATHETER SEPSIS ( 25 FDA reports)
CEREBELLAR ATROPHY ( 25 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 25 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 25 FDA reports)
CONCUSSION ( 25 FDA reports)
DEVICE OCCLUSION ( 25 FDA reports)
DYSPAREUNIA ( 25 FDA reports)
EXTREMITY CONTRACTURE ( 25 FDA reports)
FEELING DRUNK ( 25 FDA reports)
FEELINGS OF WORTHLESSNESS ( 25 FDA reports)
FLAT AFFECT ( 25 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 25 FDA reports)
HEPATIC ENCEPHALOPATHY ( 25 FDA reports)
HUNGER ( 25 FDA reports)
INCISIONAL HERNIA ( 25 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 25 FDA reports)
INTRACARDIAC THROMBUS ( 25 FDA reports)
ISCHAEMIC HEPATITIS ( 25 FDA reports)
JOINT CONTRACTURE ( 25 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 25 FDA reports)
MENOPAUSE ( 25 FDA reports)
MUSCLE INJURY ( 25 FDA reports)
MYDRIASIS ( 25 FDA reports)
NASAL POLYPS ( 25 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 25 FDA reports)
OEDEMA MUCOSAL ( 25 FDA reports)
ORCHITIS ( 25 FDA reports)
PAROTITIS ( 25 FDA reports)
POOR PERIPHERAL CIRCULATION ( 25 FDA reports)
PREMATURE BABY ( 25 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 25 FDA reports)
RESPIRATORY TRACT INFECTION ( 25 FDA reports)
TORSADE DE POINTES ( 25 FDA reports)
URINE ANALYSIS ABNORMAL ( 25 FDA reports)
VENOUS THROMBOSIS LIMB ( 25 FDA reports)
SHOULDER PAIN ( 24 FDA reports)
SUICIDAL BEHAVIOUR ( 24 FDA reports)
SUPERINFECTION ( 24 FDA reports)
TRANSFUSION REACTION ( 24 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 24 FDA reports)
VEIN DISORDER ( 24 FDA reports)
VOCAL CORD DISORDER ( 24 FDA reports)
BILE DUCT OBSTRUCTION ( 24 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 24 FDA reports)
BLOOD PROLACTIN INCREASED ( 24 FDA reports)
BREAST CYST ( 24 FDA reports)
BUNDLE BRANCH BLOCK ( 24 FDA reports)
EXTREMITY NECROSIS ( 24 FDA reports)
FANCONI SYNDROME ( 24 FDA reports)
HELICOBACTER INFECTION ( 24 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 24 FDA reports)
IMPLANT SITE INFECTION ( 24 FDA reports)
JAUNDICE CHOLESTATIC ( 24 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 24 FDA reports)
KNEE OPERATION ( 24 FDA reports)
MENISCUS REMOVAL ( 24 FDA reports)
MENOPAUSAL SYMPTOMS ( 24 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 24 FDA reports)
MUSCLE SPASTICITY ( 24 FDA reports)
MYOPIA ( 24 FDA reports)
NASAL SEPTUM DEVIATION ( 24 FDA reports)
OESOPHAGEAL SPASM ( 24 FDA reports)
ONYCHALGIA ( 24 FDA reports)
PERIPHERAL EMBOLISM ( 24 FDA reports)
PORTAL HYPERTENSION ( 24 FDA reports)
PREGNANCY ( 24 FDA reports)
RASH PAPULAR ( 24 FDA reports)
RENAL CANCER ( 24 FDA reports)
ABNORMAL FAECES ( 23 FDA reports)
APHTHOUS STOMATITIS ( 23 FDA reports)
ASPERGILLOSIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 23 FDA reports)
BILIARY COLIC ( 23 FDA reports)
BLOOD CHLORIDE INCREASED ( 23 FDA reports)
BONE MARROW OEDEMA ( 23 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 23 FDA reports)
BURNS THIRD DEGREE ( 23 FDA reports)
CAECITIS ( 23 FDA reports)
CHEILITIS ( 23 FDA reports)
CLAVICLE FRACTURE ( 23 FDA reports)
DEMYELINATION ( 23 FDA reports)
DEVICE MALFUNCTION ( 23 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 23 FDA reports)
ECZEMA ASTEATOTIC ( 23 FDA reports)
GINGIVAL ATROPHY ( 23 FDA reports)
GINGIVAL EROSION ( 23 FDA reports)
HERNIA ( 23 FDA reports)
ICHTHYOSIS ( 23 FDA reports)
INTESTINAL HAEMORRHAGE ( 23 FDA reports)
KNEE ARTHROPLASTY ( 23 FDA reports)
LARYNGOSPASM ( 23 FDA reports)
LOW TURNOVER OSTEOPATHY ( 23 FDA reports)
MENSTRUAL DISORDER ( 23 FDA reports)
METABOLIC ALKALOSIS ( 23 FDA reports)
NYSTAGMUS ( 23 FDA reports)
ORAL MUCOSA ATROPHY ( 23 FDA reports)
ORGAN FAILURE ( 23 FDA reports)
PLACENTAL INFARCTION ( 23 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 23 FDA reports)
SELF-MEDICATION ( 23 FDA reports)
TOBACCO ABUSE ( 23 FDA reports)
WOUND SECRETION ( 23 FDA reports)
SCREAMING ( 22 FDA reports)
SEROTONIN SYNDROME ( 22 FDA reports)
SINUSITIS FUNGAL ( 22 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 22 FDA reports)
TINEA INFECTION ( 22 FDA reports)
TONGUE DISCOLOURATION ( 22 FDA reports)
TOOTH DISCOLOURATION ( 22 FDA reports)
TRIGGER FINGER ( 22 FDA reports)
VISUAL FIELD DEFECT ( 22 FDA reports)
ABDOMINAL MASS ( 22 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 22 FDA reports)
ADDISON'S DISEASE ( 22 FDA reports)
AGEUSIA ( 22 FDA reports)
APPLICATION SITE RASH ( 22 FDA reports)
BIOPSY BONE ABNORMAL ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 22 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
CATATONIA ( 22 FDA reports)
CEREBROVASCULAR DISORDER ( 22 FDA reports)
CLOSTRIDIUM COLITIS ( 22 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 22 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 22 FDA reports)
DRUG PRESCRIBING ERROR ( 22 FDA reports)
EATING DISORDER SYMPTOM ( 22 FDA reports)
EPIDIDYMITIS ( 22 FDA reports)
GALACTORRHOEA ( 22 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 22 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 22 FDA reports)
HERNIA REPAIR ( 22 FDA reports)
HYPERMETABOLISM ( 22 FDA reports)
HYSTERECTOMY ( 22 FDA reports)
LICHENOID KERATOSIS ( 22 FDA reports)
MACROCYTOSIS ( 22 FDA reports)
MEDICAL DEVICE COMPLICATION ( 22 FDA reports)
MEDICAL DEVICE REMOVAL ( 22 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 22 FDA reports)
PLASTIC SURGERY TO THE FACE ( 22 FDA reports)
PUPILS UNEQUAL ( 22 FDA reports)
RADIATION ASSOCIATED PAIN ( 22 FDA reports)
AEROMONA INFECTION ( 21 FDA reports)
BK VIRUS INFECTION ( 21 FDA reports)
BLINDNESS TRANSIENT ( 21 FDA reports)
BRONCHOPNEUMONIA ( 21 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 21 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 21 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 21 FDA reports)
CONDUCTION DISORDER ( 21 FDA reports)
CULTURE POSITIVE ( 21 FDA reports)
DYSPHORIA ( 21 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 21 FDA reports)
FIBRIN D DIMER INCREASED ( 21 FDA reports)
FRUSTRATION ( 21 FDA reports)
GASTROINTESTINAL PAIN ( 21 FDA reports)
HANGOVER ( 21 FDA reports)
HYPERTROPHY ( 21 FDA reports)
INAPPROPRIATE AFFECT ( 21 FDA reports)
INDURATION ( 21 FDA reports)
INFECTIOUS PERITONITIS ( 21 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 21 FDA reports)
KELOID SCAR ( 21 FDA reports)
LABYRINTHITIS ( 21 FDA reports)
LACTOSE INTOLERANCE ( 21 FDA reports)
LEG AMPUTATION ( 21 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 21 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 21 FDA reports)
MUCOSAL ULCERATION ( 21 FDA reports)
NAIL DYSTROPHY ( 21 FDA reports)
NERVE INJURY ( 21 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 21 FDA reports)
OESOPHAGEAL STENOSIS ( 21 FDA reports)
ORTHODONTIC APPLIANCE USER ( 21 FDA reports)
PHOBIA ( 21 FDA reports)
PHOTOSENSITIVITY REACTION ( 21 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 21 FDA reports)
PULMONARY GRANULOMA ( 21 FDA reports)
RADIATION OESOPHAGITIS ( 21 FDA reports)
SECRETION DISCHARGE ( 21 FDA reports)
SELF MUTILATION ( 21 FDA reports)
SKIN NECROSIS ( 21 FDA reports)
SPINAL FUSION SURGERY ( 21 FDA reports)
STATUS EPILEPTICUS ( 21 FDA reports)
STRESS SYMPTOMS ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
TESTICULAR PAIN ( 21 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 21 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 21 FDA reports)
VENOUS THROMBOSIS ( 21 FDA reports)
VULVOVAGINAL PRURITUS ( 21 FDA reports)
WEIGHT BEARING DIFFICULTY ( 21 FDA reports)
RIGHT VENTRICULAR FAILURE ( 20 FDA reports)
SCOTOMA ( 20 FDA reports)
SKIN FRAGILITY ( 20 FDA reports)
SKIN REACTION ( 20 FDA reports)
SPLENIC INFARCTION ( 20 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 20 FDA reports)
TONGUE COATED ( 20 FDA reports)
VASCULAR ANOMALY ( 20 FDA reports)
VASCULAR CALCIFICATION ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
WOUND DECOMPOSITION ( 20 FDA reports)
BILIARY DYSKINESIA ( 20 FDA reports)
BLOOD COUNT ABNORMAL ( 20 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 20 FDA reports)
BLOOD SODIUM INCREASED ( 20 FDA reports)
CALCULUS URETERIC ( 20 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 20 FDA reports)
COLLAPSE OF LUNG ( 20 FDA reports)
COLON ADENOMA ( 20 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 20 FDA reports)
DEREALISATION ( 20 FDA reports)
DIABETIC GASTROPARESIS ( 20 FDA reports)
DRY THROAT ( 20 FDA reports)
DYSMENORRHOEA ( 20 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 20 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 20 FDA reports)
FOLLICULITIS ( 20 FDA reports)
FOOD CRAVING ( 20 FDA reports)
FOOD POISONING ( 20 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 20 FDA reports)
GLYCOSURIA ( 20 FDA reports)
HAEMORRHAGIC STROKE ( 20 FDA reports)
HYDROCELE ( 20 FDA reports)
HYPERMETROPIA ( 20 FDA reports)
IMPAIRED SELF-CARE ( 20 FDA reports)
JUDGEMENT IMPAIRED ( 20 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 20 FDA reports)
MAMMOGRAM ABNORMAL ( 20 FDA reports)
MENSTRUATION IRREGULAR ( 20 FDA reports)
METASTASES TO THORAX ( 20 FDA reports)
MITRAL VALVE CALCIFICATION ( 20 FDA reports)
NEPHROTIC SYNDROME ( 20 FDA reports)
NERVE ROOT LESION ( 20 FDA reports)
NEURODERMATITIS ( 20 FDA reports)
NO ADVERSE EVENT ( 20 FDA reports)
NON-SMALL CELL LUNG CANCER ( 20 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 20 FDA reports)
OSTEOCHONDROSIS ( 20 FDA reports)
PANCREATIC DISORDER ( 20 FDA reports)
PARTIAL SEIZURES ( 20 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 20 FDA reports)
PULMONARY TOXICITY ( 20 FDA reports)
RENAL ARTERY STENOSIS ( 20 FDA reports)
RENAL ISCHAEMIA ( 20 FDA reports)
RESPIRATORY ACIDOSIS ( 20 FDA reports)
ABSCESS NECK ( 19 FDA reports)
ALVEOLAR OSTEITIS ( 19 FDA reports)
ANISOCYTOSIS ( 19 FDA reports)
BLOOD URIC ACID INCREASED ( 19 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 19 FDA reports)
BREAST CANCER IN SITU ( 19 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 19 FDA reports)
CARDIAC VALVE ABSCESS ( 19 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 19 FDA reports)
COLON POLYPECTOMY ( 19 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 19 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 19 FDA reports)
DRUG ERUPTION ( 19 FDA reports)
EAR HAEMORRHAGE ( 19 FDA reports)
ENDOMETRIAL CANCER ( 19 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 19 FDA reports)
ENTEROCUTANEOUS FISTULA ( 19 FDA reports)
EYE DISCHARGE ( 19 FDA reports)
FAMILY STRESS ( 19 FDA reports)
GRAFT INFECTION ( 19 FDA reports)
HALLUCINATIONS, MIXED ( 19 FDA reports)
HEPATITIS CHOLESTATIC ( 19 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 19 FDA reports)
INFARCTION ( 19 FDA reports)
LARYNGOCELE ( 19 FDA reports)
LIP ULCERATION ( 19 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 19 FDA reports)
MEDICATION RESIDUE ( 19 FDA reports)
MULTIPLE FRACTURES ( 19 FDA reports)
NEOPLASM RECURRENCE ( 19 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 19 FDA reports)
OOPHORECTOMY ( 19 FDA reports)
OTORRHOEA ( 19 FDA reports)
PANCREATIC CYST ( 19 FDA reports)
PHYSICAL ASSAULT ( 19 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 19 FDA reports)
POSTURE ABNORMAL ( 19 FDA reports)
PULMONARY THROMBOSIS ( 19 FDA reports)
PULPITIS DENTAL ( 19 FDA reports)
PYELOCALIECTASIS ( 19 FDA reports)
REGURGITATION ( 19 FDA reports)
RIGHT ATRIAL DILATATION ( 19 FDA reports)
SALPINGITIS ( 19 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 19 FDA reports)
SEBORRHOEA ( 19 FDA reports)
SKIN WARM ( 19 FDA reports)
SPINAL PAIN ( 19 FDA reports)
TELANGIECTASIA ( 19 FDA reports)
TONGUE OEDEMA ( 19 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 19 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 19 FDA reports)
VITAMIN D DECREASED ( 19 FDA reports)
WOUND DEBRIDEMENT ( 19 FDA reports)
SPONDYLOLYSIS ( 18 FDA reports)
SPUTUM CULTURE POSITIVE ( 18 FDA reports)
STOMATOCYTES PRESENT ( 18 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 18 FDA reports)
TESTICULAR SWELLING ( 18 FDA reports)
TINEA PEDIS ( 18 FDA reports)
TRACHEOSTOMY ( 18 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 18 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 18 FDA reports)
WRONG DRUG ADMINISTERED ( 18 FDA reports)
ABNORMAL SENSATION IN EYE ( 18 FDA reports)
ABSCESS INTESTINAL ( 18 FDA reports)
ANORECTAL DISORDER ( 18 FDA reports)
APLASTIC ANAEMIA ( 18 FDA reports)
ARTERIAL THROMBOSIS ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ASTIGMATISM ( 18 FDA reports)
BILIARY DILATATION ( 18 FDA reports)
BLADDER DILATATION ( 18 FDA reports)
BLADDER OBSTRUCTION ( 18 FDA reports)
BLOOD BICARBONATE DECREASED ( 18 FDA reports)
BLOOD TEST ABNORMAL ( 18 FDA reports)
BREAST LUMP REMOVAL ( 18 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 18 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 18 FDA reports)
CUBITAL TUNNEL SYNDROME ( 18 FDA reports)
DERMATITIS ATOPIC ( 18 FDA reports)
DERMOID CYST ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
EJACULATION DISORDER ( 18 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 18 FDA reports)
EXTERNAL EAR DISORDER ( 18 FDA reports)
EYE INFECTION ( 18 FDA reports)
GALLBLADDER ENLARGEMENT ( 18 FDA reports)
GOUTY ARTHRITIS ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 18 FDA reports)
HEPATOCELLULAR DAMAGE ( 18 FDA reports)
HEPATOTOXICITY ( 18 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 18 FDA reports)
HYPERREFLEXIA ( 18 FDA reports)
HYPOTHERMIA ( 18 FDA reports)
IMMUNE SYSTEM DISORDER ( 18 FDA reports)
INJECTION SITE SWELLING ( 18 FDA reports)
IRREGULAR SLEEP PHASE ( 18 FDA reports)
JUGULAR VEIN DISTENSION ( 18 FDA reports)
LIMB CRUSHING INJURY ( 18 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 18 FDA reports)
MITRAL VALVE SCLEROSIS ( 18 FDA reports)
MORGANELLA INFECTION ( 18 FDA reports)
NASAL DISORDER ( 18 FDA reports)
NEUROFIBROMA ( 18 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 18 FDA reports)
PERIORBITAL OEDEMA ( 18 FDA reports)
POIKILOCYTOSIS ( 18 FDA reports)
POLYPECTOMY ( 18 FDA reports)
POOR VENOUS ACCESS ( 18 FDA reports)
POST PROCEDURAL FISTULA ( 18 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
RASH MORBILLIFORM ( 18 FDA reports)
REFLUX GASTRITIS ( 18 FDA reports)
ABDOMINAL ADHESIONS ( 17 FDA reports)
ALCOHOL POISONING ( 17 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 17 FDA reports)
ANGIOPLASTY ( 17 FDA reports)
AORTIC DISORDER ( 17 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 17 FDA reports)
ASPIRATION PLEURAL CAVITY ( 17 FDA reports)
ATRIAL TACHYCARDIA ( 17 FDA reports)
AXILLARY MASS ( 17 FDA reports)
BLADDER CYST ( 17 FDA reports)
BLADDER PROLAPSE ( 17 FDA reports)
BONE DENSITY INCREASED ( 17 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 17 FDA reports)
BREAST INDURATION ( 17 FDA reports)
BREAST OPERATION ( 17 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 17 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 17 FDA reports)
COLON CANCER METASTATIC ( 17 FDA reports)
CYSTITIS INTERSTITIAL ( 17 FDA reports)
DENTAL TREATMENT ( 17 FDA reports)
DYSPLASIA ( 17 FDA reports)
EOSINOPHIL COUNT DECREASED ( 17 FDA reports)
GINGIVAL OPERATION ( 17 FDA reports)
HAEMOPHILUS INFECTION ( 17 FDA reports)
HAEMOTHORAX ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HIGH FREQUENCY ABLATION ( 17 FDA reports)
INCISION SITE INFECTION ( 17 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 17 FDA reports)
LACTIC ACIDOSIS ( 17 FDA reports)
LARYNGEAL OEDEMA ( 17 FDA reports)
MASS EXCISION ( 17 FDA reports)
MENINGITIS ASEPTIC ( 17 FDA reports)
METAPLASIA ( 17 FDA reports)
METRORRHAGIA ( 17 FDA reports)
MICTURITION DISORDER ( 17 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 17 FDA reports)
NAIL AVULSION ( 17 FDA reports)
NEUROENDOCRINE CARCINOMA ( 17 FDA reports)
NEUROLOGICAL SYMPTOM ( 17 FDA reports)
OCULAR ICTERUS ( 17 FDA reports)
OPTIC NEUROPATHY ( 17 FDA reports)
ORAL DISCHARGE ( 17 FDA reports)
ORAL FUNGAL INFECTION ( 17 FDA reports)
OSTEOSARCOMA METASTATIC ( 17 FDA reports)
OVARIAN FAILURE ( 17 FDA reports)
OVARIAN MASS ( 17 FDA reports)
PANCREATIC NEOPLASM ( 17 FDA reports)
PERIODONTAL DESTRUCTION ( 17 FDA reports)
PERIRECTAL ABSCESS ( 17 FDA reports)
PITTING OEDEMA ( 17 FDA reports)
PNEUMONIA BACTERIAL ( 17 FDA reports)
POSTNASAL DRIP ( 17 FDA reports)
PROSTATITIS ( 17 FDA reports)
QUADRIPLEGIA ( 17 FDA reports)
SKIN ATROPHY ( 17 FDA reports)
SKIN HAEMORRHAGE ( 17 FDA reports)
SMEAR CERVIX ABNORMAL ( 17 FDA reports)
STENT PLACEMENT ( 17 FDA reports)
TOBACCO USER ( 17 FDA reports)
TUMOUR MARKER INCREASED ( 17 FDA reports)
URINE ODOUR ABNORMAL ( 17 FDA reports)
VASCULAR PSEUDOANEURYSM ( 17 FDA reports)
YELLOW SKIN ( 17 FDA reports)
SCLERODERMA ( 16 FDA reports)
SCRATCH ( 16 FDA reports)
SEPSIS SYNDROME ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SICK SINUS SYNDROME ( 16 FDA reports)
SIMPLE PARTIAL SEIZURES ( 16 FDA reports)
SOCIAL PROBLEM ( 16 FDA reports)
SOFT TISSUE INFLAMMATION ( 16 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 16 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 16 FDA reports)
TONGUE PARALYSIS ( 16 FDA reports)
VENTRICULAR ARRHYTHMIA ( 16 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 16 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 16 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 16 FDA reports)
AMMONIA INCREASED ( 16 FDA reports)
ANAEMIA MACROCYTIC ( 16 FDA reports)
ANGIOMYOLIPOMA ( 16 FDA reports)
BACTERIA STOOL IDENTIFIED ( 16 FDA reports)
BASOSQUAMOUS CARCINOMA ( 16 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 16 FDA reports)
BLOOD CREATINE INCREASED ( 16 FDA reports)
BONE CALLUS EXCESSIVE ( 16 FDA reports)
BONE MARROW DISORDER ( 16 FDA reports)
BRAIN MASS ( 16 FDA reports)
BREAST PROSTHESIS USER ( 16 FDA reports)
BUTTOCK PAIN ( 16 FDA reports)
CAROTID ARTERY OCCLUSION ( 16 FDA reports)
CERVICAL MYELOPATHY ( 16 FDA reports)
CHANGE OF BOWEL HABIT ( 16 FDA reports)
COLONIC OBSTRUCTION ( 16 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 16 FDA reports)
CREPITATIONS ( 16 FDA reports)
DEVICE RELATED SEPSIS ( 16 FDA reports)
DIVERTICULAR PERFORATION ( 16 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 16 FDA reports)
ENCEPHALITIS ( 16 FDA reports)
ESCHERICHIA SEPSIS ( 16 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 16 FDA reports)
EXPIRED DRUG ADMINISTERED ( 16 FDA reports)
FACIAL NERVE DISORDER ( 16 FDA reports)
FOAMING AT MOUTH ( 16 FDA reports)
FOOD INTOLERANCE ( 16 FDA reports)
GRANDIOSITY ( 16 FDA reports)
HEPATIC CONGESTION ( 16 FDA reports)
HEPATIC ENZYME ABNORMAL ( 16 FDA reports)
HEPATIC MASS ( 16 FDA reports)
INFUSION SITE ERYTHEMA ( 16 FDA reports)
INTESTINAL POLYP ( 16 FDA reports)
INTRACRANIAL HYPOTENSION ( 16 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
LYMPHADENITIS ( 16 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 16 FDA reports)
MAMMOPLASTY ( 16 FDA reports)
METASTASES TO MENINGES ( 16 FDA reports)
MIOSIS ( 16 FDA reports)
MUCOSAL HAEMORRHAGE ( 16 FDA reports)
MYELOPATHY ( 16 FDA reports)
NEUTROPENIC SEPSIS ( 16 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
OPTIC NERVE DISORDER ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PAPULE ( 16 FDA reports)
PARATHYROID TUMOUR BENIGN ( 16 FDA reports)
PARONYCHIA ( 16 FDA reports)
PELVIC ABSCESS ( 16 FDA reports)
PILONIDAL CYST ( 16 FDA reports)
POSTMENOPAUSE ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
AUTOIMMUNE HEPATITIS ( 15 FDA reports)
BLOOD CORTISOL ABNORMAL ( 15 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 15 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 15 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 15 FDA reports)
BONE MARROW DEPRESSION ( 15 FDA reports)
BRAIN DAMAGE ( 15 FDA reports)
BREAST DISCHARGE ( 15 FDA reports)
CALCINOSIS ( 15 FDA reports)
CARDIAC ENZYMES INCREASED ( 15 FDA reports)
CARDIOPULMONARY FAILURE ( 15 FDA reports)
CARTILAGE ATROPHY ( 15 FDA reports)
CERVICAL CORD COMPRESSION ( 15 FDA reports)
CHONDROMALACIA ( 15 FDA reports)
COR PULMONALE ( 15 FDA reports)
CORNEAL ABRASION ( 15 FDA reports)
DENTAL DISCOMFORT ( 15 FDA reports)
DEVICE LEAKAGE ( 15 FDA reports)
DRUG DISPENSING ERROR ( 15 FDA reports)
FACTOR V LEIDEN MUTATION ( 15 FDA reports)
FAECES HARD ( 15 FDA reports)
GALLBLADDER INJURY ( 15 FDA reports)
GASTROINTESTINAL PERFORATION ( 15 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 15 FDA reports)
HAEMORRHAGIC ANAEMIA ( 15 FDA reports)
HAIR TEXTURE ABNORMAL ( 15 FDA reports)
HEPATOSPLENOMEGALY ( 15 FDA reports)
HYPERPHOSPHATAEMIA ( 15 FDA reports)
HYPERTONIC BLADDER ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
INJECTION SITE INDURATION ( 15 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 15 FDA reports)
LEUKAEMIA RECURRENT ( 15 FDA reports)
LIGHT CHAIN ANALYSIS ( 15 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 15 FDA reports)
LUNG ADENOCARCINOMA ( 15 FDA reports)
MALABSORPTION ( 15 FDA reports)
MONOCYTE COUNT DECREASED ( 15 FDA reports)
MUSCLE CONTRACTURE ( 15 FDA reports)
NODAL OSTEOARTHRITIS ( 15 FDA reports)
OPEN ANGLE GLAUCOMA ( 15 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 15 FDA reports)
PATELLA FRACTURE ( 15 FDA reports)
PCO2 DECREASED ( 15 FDA reports)
PERICARDIAL HAEMORRHAGE ( 15 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 15 FDA reports)
PROTEIN URINE ABSENT ( 15 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 15 FDA reports)
ROSACEA ( 15 FDA reports)
SENSATION OF PRESSURE ( 15 FDA reports)
SLUGGISHNESS ( 15 FDA reports)
SNEEZING ( 15 FDA reports)
SPONDYLITIS ( 15 FDA reports)
STATUS ASTHMATICUS ( 15 FDA reports)
STRESS INCONTINENCE ( 15 FDA reports)
TEMPERATURE INTOLERANCE ( 15 FDA reports)
TUMOUR LYSIS SYNDROME ( 15 FDA reports)
VERBAL ABUSE ( 15 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 15 FDA reports)
SALIVARY GLAND MASS ( 14 FDA reports)
SJOGREN'S SYNDROME ( 14 FDA reports)
SPLENIC ARTERY ANEURYSM ( 14 FDA reports)
TENSION HEADACHE ( 14 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 14 FDA reports)
TONSILLAR DISORDER ( 14 FDA reports)
TRACHEOBRONCHITIS ( 14 FDA reports)
TRIGEMINAL NEURALGIA ( 14 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
VASCULAR DEMENTIA ( 14 FDA reports)
VITAMIN B12 DECREASED ( 14 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 14 FDA reports)
ADNEXA UTERI MASS ( 14 FDA reports)
ALLERGY TO ANIMAL ( 14 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 14 FDA reports)
AORTIC THROMBOSIS ( 14 FDA reports)
APHONIA ( 14 FDA reports)
ATHEROSCLEROSIS ( 14 FDA reports)
BASEDOW'S DISEASE ( 14 FDA reports)
BENIGN BREAST NEOPLASM ( 14 FDA reports)
BILIARY TRACT DISORDER ( 14 FDA reports)
BIOPSY BREAST ABNORMAL ( 14 FDA reports)
BLOOD CREATININE DECREASED ( 14 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 14 FDA reports)
BREAST FIBROSIS ( 14 FDA reports)
BRONCHITIS CHRONIC ( 14 FDA reports)
CARDIAC FAILURE CHRONIC ( 14 FDA reports)
CHOLANGITIS ( 14 FDA reports)
COLECTOMY ( 14 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
EFFUSION ( 14 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 14 FDA reports)
ERYTHEMA OF EYELID ( 14 FDA reports)
EYE MOVEMENT DISORDER ( 14 FDA reports)
FEAR OF DEATH ( 14 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 14 FDA reports)
GENITAL HERPES ( 14 FDA reports)
HAEMANGIOMA OF LIVER ( 14 FDA reports)
HAIR GROWTH ABNORMAL ( 14 FDA reports)
HYPOPNOEA ( 14 FDA reports)
IMPRISONMENT ( 14 FDA reports)
INJURY ASPHYXIATION ( 14 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 14 FDA reports)
LEUKODYSTROPHY ( 14 FDA reports)
LIVEDO RETICULARIS ( 14 FDA reports)
LOSS OF EMPLOYMENT ( 14 FDA reports)
LUPUS-LIKE SYNDROME ( 14 FDA reports)
LYMPH NODE PAIN ( 14 FDA reports)
MEDIASTINAL DISORDER ( 14 FDA reports)
MELANOSIS COLI ( 14 FDA reports)
MENINGEAL NEOPLASM ( 14 FDA reports)
METASTASES TO PELVIS ( 14 FDA reports)
MORTON'S NEUROMA ( 14 FDA reports)
NEGATIVE THOUGHTS ( 14 FDA reports)
NEPHROPATHY TOXIC ( 14 FDA reports)
NEUTROPENIC INFECTION ( 14 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 14 FDA reports)
OBSTRUCTIVE UROPATHY ( 14 FDA reports)
OROPHARYNGEAL SWELLING ( 14 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 14 FDA reports)
PARTNER STRESS ( 14 FDA reports)
PERIOSTITIS ( 14 FDA reports)
POLYCYTHAEMIA ( 14 FDA reports)
POLYP COLORECTAL ( 14 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 14 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 14 FDA reports)
PROCTITIS ULCERATIVE ( 14 FDA reports)
RADICULITIS ( 14 FDA reports)
RASH PUSTULAR ( 14 FDA reports)
RENAL ATROPHY ( 14 FDA reports)
ABDOMINAL SEPSIS ( 13 FDA reports)
ACANTHOMA ( 13 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 13 FDA reports)
ANTISOCIAL BEHAVIOUR ( 13 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 13 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 13 FDA reports)
ASPHYXIA ( 13 FDA reports)
BILE DUCT STENOSIS ( 13 FDA reports)
BINGE EATING ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 13 FDA reports)
BLOOD MAGNESIUM INCREASED ( 13 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 13 FDA reports)
BRAIN HERNIATION ( 13 FDA reports)
BREAST CALCIFICATIONS ( 13 FDA reports)
BREAST ENLARGEMENT ( 13 FDA reports)
BREAST PROSTHESIS REMOVAL ( 13 FDA reports)
CATHETER SITE INFECTION ( 13 FDA reports)
CENTRAL LINE INFECTION ( 13 FDA reports)
CEREBRAL DISORDER ( 13 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 13 FDA reports)
CLUMSINESS ( 13 FDA reports)
COLITIS MICROSCOPIC ( 13 FDA reports)
CORONARY ARTERY THROMBOSIS ( 13 FDA reports)
DEFAECATION URGENCY ( 13 FDA reports)
DEPRESSION SUICIDAL ( 13 FDA reports)
DERMATOMYOSITIS ( 13 FDA reports)
DIABETIC EYE DISEASE ( 13 FDA reports)
DYSGRAPHIA ( 13 FDA reports)
ENCEPHALITIS HERPES ( 13 FDA reports)
ENTEROCOLITIS ( 13 FDA reports)
EXERCISE TOLERANCE DECREASED ( 13 FDA reports)
FACE INJURY ( 13 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 13 FDA reports)
FOREARM FRACTURE ( 13 FDA reports)
GASTROSTOMY TUBE INSERTION ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
HEART INJURY ( 13 FDA reports)
HIV INFECTION ( 13 FDA reports)
HYPERVISCOSITY SYNDROME ( 13 FDA reports)
HYPOTONIA ( 13 FDA reports)
IMMUNOGLOBULINS DECREASED ( 13 FDA reports)
INFUSION SITE SWELLING ( 13 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 13 FDA reports)
LENTIGO ( 13 FDA reports)
LUNG INJURY ( 13 FDA reports)
NERVE ROOT COMPRESSION ( 13 FDA reports)
OBSTRUCTION ( 13 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 13 FDA reports)
ORAL SOFT TISSUE DISORDER ( 13 FDA reports)
ORAL TORUS ( 13 FDA reports)
OROPHARYNGEAL BLISTERING ( 13 FDA reports)
OTITIS MEDIA ACUTE ( 13 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 13 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 13 FDA reports)
POLYSUBSTANCE ABUSE ( 13 FDA reports)
PRODUCT ADHESION ISSUE ( 13 FDA reports)
PROTEIN URINE PRESENT ( 13 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 13 FDA reports)
RASH VESICULAR ( 13 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 13 FDA reports)
RENAL CELL CARCINOMA ( 13 FDA reports)
SKIN INJURY ( 13 FDA reports)
SPINAL HAEMANGIOMA ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 13 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 13 FDA reports)
THYROIDITIS ( 13 FDA reports)
VERTIGO POSITIONAL ( 13 FDA reports)
VITREOUS DETACHMENT ( 13 FDA reports)
WOUND TREATMENT ( 13 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 12 FDA reports)
SKIN MASS ( 12 FDA reports)
SOFT TISSUE INFECTION ( 12 FDA reports)
SOMATOFORM DISORDER ( 12 FDA reports)
STRESS URINARY INCONTINENCE ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 12 FDA reports)
TENDON INJURY ( 12 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 12 FDA reports)
TOE AMPUTATION ( 12 FDA reports)
TOOTH INJURY ( 12 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 12 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 12 FDA reports)
URETHRAL OBSTRUCTION ( 12 FDA reports)
UTERINE PROLAPSE ( 12 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 12 FDA reports)
VITAMIN A DEFICIENCY ( 12 FDA reports)
VITAMIN K DEFICIENCY ( 12 FDA reports)
VOCAL CORD POLYP ( 12 FDA reports)
WEIGHT LOSS POOR ( 12 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 12 FDA reports)
ADRENAL ADENOMA ( 12 FDA reports)
AMBLYOPIA ( 12 FDA reports)
ANGIONEUROTIC OEDEMA ( 12 FDA reports)
APPLICATION SITE IRRITATION ( 12 FDA reports)
ARTHROSCOPIC SURGERY ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
AXONAL NEUROPATHY ( 12 FDA reports)
BARTHOLIN'S ABSCESS ( 12 FDA reports)
BARTHOLIN'S CYST ( 12 FDA reports)
BENCE JONES PROTEINURIA ( 12 FDA reports)
BENIGN COLONIC NEOPLASM ( 12 FDA reports)
BENIGN TUMOUR EXCISION ( 12 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 12 FDA reports)
BIOPSY LYMPH GLAND ( 12 FDA reports)
BLEPHAROSPASM ( 12 FDA reports)
BLOOD DISORDER ( 12 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 12 FDA reports)
BLOOD IRON DECREASED ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 12 FDA reports)
BONE CYST ( 12 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 12 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 12 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 12 FDA reports)
CHOKING SENSATION ( 12 FDA reports)
CHROMATOPSIA ( 12 FDA reports)
CLUSTER HEADACHE ( 12 FDA reports)
CONGENITAL ANOMALY ( 12 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 12 FDA reports)
DRUG CLEARANCE DECREASED ( 12 FDA reports)
DRUG EFFECT INCREASED ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 12 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 12 FDA reports)
EMBOLISM ARTERIAL ( 12 FDA reports)
EXCESSIVE EYE BLINKING ( 12 FDA reports)
EYELID MARGIN CRUSTING ( 12 FDA reports)
FLASHBACK ( 12 FDA reports)
GLIOSIS ( 12 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 12 FDA reports)
HEAD DISCOMFORT ( 12 FDA reports)
HIDRADENITIS ( 12 FDA reports)
HYPERTENSIVE CRISIS ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
INCREASED BRONCHIAL SECRETION ( 12 FDA reports)
INJECTION SITE BRUISING ( 12 FDA reports)
INJECTION SITE MASS ( 12 FDA reports)
INJECTION SITE WARMTH ( 12 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 12 FDA reports)
IRON DEFICIENCY ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
LISTLESS ( 12 FDA reports)
LOSS OF CONTROL OF LEGS ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
LUNG CANCER METASTATIC ( 12 FDA reports)
LYME DISEASE ( 12 FDA reports)
LYMPHOCYTOSIS ( 12 FDA reports)
MALIGNANT HYPERTENSION ( 12 FDA reports)
MASTOCYTOSIS ( 12 FDA reports)
MIDDLE EAR EFFUSION ( 12 FDA reports)
MITRAL VALVE REPLACEMENT ( 12 FDA reports)
MOUTH CYST ( 12 FDA reports)
NASAL SINUS CANCER ( 12 FDA reports)
NASAL ULCER ( 12 FDA reports)
NEUROTOXICITY ( 12 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 12 FDA reports)
OBSESSIVE THOUGHTS ( 12 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 12 FDA reports)
OPTIC NEURITIS ( 12 FDA reports)
OTITIS MEDIA CHRONIC ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PERICARDIAL DRAINAGE ( 12 FDA reports)
PLEURODESIS ( 12 FDA reports)
PNEUMONIA VIRAL ( 12 FDA reports)
POST LAMINECTOMY SYNDROME ( 12 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 12 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 12 FDA reports)
PRESBYOESOPHAGUS ( 12 FDA reports)
RADICULITIS LUMBOSACRAL ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
RENAL MASS ( 12 FDA reports)
RESPIRATION ABNORMAL ( 12 FDA reports)
RETINAL HAEMORRHAGE ( 12 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 11 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
ANAEMIA POSTOPERATIVE ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 11 FDA reports)
ANION GAP INCREASED ( 11 FDA reports)
APPARENT DEATH ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 11 FDA reports)
B-CELL LYMPHOMA ( 11 FDA reports)
BIOPSY BONE MARROW ( 11 FDA reports)
BIOPSY MUSCLE ( 11 FDA reports)
BIOPSY PERIPHERAL NERVE ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD PH INCREASED ( 11 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 11 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 11 FDA reports)
BLOOD URINE ( 11 FDA reports)
BONE GRAFT ( 11 FDA reports)
BREAST HYPERPLASIA ( 11 FDA reports)
BRONCHIAL OBSTRUCTION ( 11 FDA reports)
CARDIAC FAILURE ACUTE ( 11 FDA reports)
CARDIAC SEPTAL DEFECT ( 11 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 11 FDA reports)
CEREBELLAR INFARCTION ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CHEST WALL MASS ( 11 FDA reports)
COLONOSCOPY ABNORMAL ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DIPLEGIA ( 11 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 11 FDA reports)
DYSPHASIA ( 11 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 11 FDA reports)
ENURESIS ( 11 FDA reports)
ESCHERICHIA BACTERAEMIA ( 11 FDA reports)
FAT NECROSIS ( 11 FDA reports)
FEEDING TUBE COMPLICATION ( 11 FDA reports)
FEELING HOT AND COLD ( 11 FDA reports)
FEMORAL ARTERY OCCLUSION ( 11 FDA reports)
FISTULA REPAIR ( 11 FDA reports)
FUNGAL RHINITIS ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
GASTRIC PERFORATION ( 11 FDA reports)
GASTROINTESTINAL NECROSIS ( 11 FDA reports)
GENITOURINARY TRACT INFECTION ( 11 FDA reports)
GLARE ( 11 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 11 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
KLEBSIELLA BACTERAEMIA ( 11 FDA reports)
LABILE BLOOD PRESSURE ( 11 FDA reports)
LAGOPHTHALMOS ( 11 FDA reports)
LEUKAEMIA ( 11 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 11 FDA reports)
LOOSE BODY IN JOINT ( 11 FDA reports)
LUNG ABSCESS ( 11 FDA reports)
LYMPH NODE PALPABLE ( 11 FDA reports)
MACROPHAGES INCREASED ( 11 FDA reports)
MACULE ( 11 FDA reports)
MACULOPATHY ( 11 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 11 FDA reports)
MENINGOMYELOCELE ( 11 FDA reports)
METASTASES TO PLEURA ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
MONARTHRITIS ( 11 FDA reports)
MOUTH INJURY ( 11 FDA reports)
MUCOSAL EROSION ( 11 FDA reports)
MUCOUS MEMBRANE DISORDER ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
MULTIPLE ALLERGIES ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
NASAL DRYNESS ( 11 FDA reports)
NASAL OBSTRUCTION ( 11 FDA reports)
NERVE COMPRESSION ( 11 FDA reports)
NEUROMA ( 11 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 11 FDA reports)
NIGHT BLINDNESS ( 11 FDA reports)
NUMB CHIN SYNDROME ( 11 FDA reports)
ONYCHOCLASIS ( 11 FDA reports)
PARAPARESIS ( 11 FDA reports)
PCO2 INCREASED ( 11 FDA reports)
PELVIC ADHESIONS ( 11 FDA reports)
PINEAL GLAND CYST ( 11 FDA reports)
PNEUMOMEDIASTINUM ( 11 FDA reports)
POST PROCEDURAL INFECTION ( 11 FDA reports)
PRESUMED OCULAR HISTOPLASMOSIS SYNDROME ( 11 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 11 FDA reports)
PULMONARY HILUM MASS ( 11 FDA reports)
PULSE ABNORMAL ( 11 FDA reports)
PUPIL FIXED ( 11 FDA reports)
RECTAL CANCER ( 11 FDA reports)
RENAL OSTEODYSTROPHY ( 11 FDA reports)
RETINOPATHY ( 11 FDA reports)
SEBACEOUS GLAND DISORDER ( 11 FDA reports)
SHOULDER ARTHROPLASTY ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 11 FDA reports)
SPINAL X-RAY ABNORMAL ( 11 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
STRESS AT WORK ( 11 FDA reports)
STRIDOR ( 11 FDA reports)
SUNBURN ( 11 FDA reports)
TENDON PAIN ( 11 FDA reports)
THROMBECTOMY ( 11 FDA reports)
TREATMENT FAILURE ( 11 FDA reports)
TUMOUR HAEMORRHAGE ( 11 FDA reports)
TUMOUR INVASION ( 11 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 10 FDA reports)
SEASONAL ALLERGY ( 10 FDA reports)
SOMATISATION DISORDER ( 10 FDA reports)
SUDDEN CARDIAC DEATH ( 10 FDA reports)
SYNOVIAL RUPTURE ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TRAUMATIC BRAIN INJURY ( 10 FDA reports)
TUBERCULOSIS ( 10 FDA reports)
TURNER'S SYNDROME ( 10 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 10 FDA reports)
URGE INCONTINENCE ( 10 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 10 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 10 FDA reports)
VAGINITIS BACTERIAL ( 10 FDA reports)
VARICELLA ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VENOUS STASIS ( 10 FDA reports)
VERTEBRAL COLUMN MASS ( 10 FDA reports)
ACCIDENTAL EXPOSURE ( 10 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ADRENAL SUPPRESSION ( 10 FDA reports)
ALCOHOL INTERACTION ( 10 FDA reports)
ALVEOLITIS ALLERGIC ( 10 FDA reports)
ANAL CANCER ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANORECTAL DISCOMFORT ( 10 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 10 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 10 FDA reports)
AORTIC DILATATION ( 10 FDA reports)
AORTIC DISSECTION ( 10 FDA reports)
ARTHRITIS INFECTIVE ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BLADDER DYSFUNCTION ( 10 FDA reports)
BLOOD ALCOHOL INCREASED ( 10 FDA reports)
BLOOD UREA DECREASED ( 10 FDA reports)
BONE NEOPLASM ( 10 FDA reports)
BRAIN OPERATION ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
BUNION ( 10 FDA reports)
CARDIAC VALVE SCLEROSIS ( 10 FDA reports)
CATHETER SITE HAEMATOMA ( 10 FDA reports)
CEREBRAL HAEMATOMA ( 10 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 10 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 10 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
CSF TEST ABNORMAL ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DIABETIC ULCER ( 10 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 10 FDA reports)
EMBOLISM VENOUS ( 10 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 10 FDA reports)
ENTEROBACTER INFECTION ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
EXTRADURAL ABSCESS ( 10 FDA reports)
FEMALE STERILISATION ( 10 FDA reports)
FOREIGN BODY REACTION ( 10 FDA reports)
GASTRIC DILATATION ( 10 FDA reports)
GENERALISED ERYTHEMA ( 10 FDA reports)
GINGIVECTOMY ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAEMOGLOBIN INCREASED ( 10 FDA reports)
HEAD BANGING ( 10 FDA reports)
INFECTIVE TENOSYNOVITIS ( 10 FDA reports)
INJECTION SITE DISCOLOURATION ( 10 FDA reports)
INJECTION SITE URTICARIA ( 10 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 10 FDA reports)
INTRA-UTERINE DEATH ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
MASTOIDITIS ( 10 FDA reports)
MEDIASTINUM NEOPLASM ( 10 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 10 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 10 FDA reports)
METATARSALGIA ( 10 FDA reports)
MIGRAINE WITH AURA ( 10 FDA reports)
MYELITIS TRANSVERSE ( 10 FDA reports)
NARCOLEPSY ( 10 FDA reports)
NONSPECIFIC REACTION ( 10 FDA reports)
OVARIAN ADHESION ( 10 FDA reports)
PAINFUL DEFAECATION ( 10 FDA reports)
PALLIATIVE CARE ( 10 FDA reports)
PARANOID PERSONALITY DISORDER ( 10 FDA reports)
PARAPROTEINAEMIA ( 10 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 10 FDA reports)
PELVIC VENOUS THROMBOSIS ( 10 FDA reports)
PERIPHERAL NERVE LESION ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 10 FDA reports)
POLYARTHRITIS ( 10 FDA reports)
POTENTIATING DRUG INTERACTION ( 10 FDA reports)
PREMATURE LABOUR ( 10 FDA reports)
PROCEDURAL NAUSEA ( 10 FDA reports)
PROCEDURAL VOMITING ( 10 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 10 FDA reports)
PSORIATIC ARTHROPATHY ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 10 FDA reports)
PYODERMA GANGRENOSUM ( 10 FDA reports)
RADIATION SKIN INJURY ( 10 FDA reports)
RADICAL HYSTERECTOMY ( 10 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 10 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 10 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ACCELERATED HYPERTENSION ( 9 FDA reports)
ACROCHORDON ( 9 FDA reports)
ACUTE ABDOMEN ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 9 FDA reports)
ANOREXIA NERVOSA ( 9 FDA reports)
AORTIC VALVE DISEASE ( 9 FDA reports)
AORTIC VALVE STENOSIS ( 9 FDA reports)
ARACHNOID CYST ( 9 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 9 FDA reports)
AUTOIMMUNE DISORDER ( 9 FDA reports)
BLOOD OESTROGEN INCREASED ( 9 FDA reports)
BLOOD PH DECREASED ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 9 FDA reports)
BOWEL SOUNDS ABNORMAL ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
BREAST CANCER STAGE I ( 9 FDA reports)
BREAST NECROSIS ( 9 FDA reports)
BREAST SWELLING ( 9 FDA reports)
CARBON DIOXIDE INCREASED ( 9 FDA reports)
CARDIAC OUTPUT DECREASED ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
CAROTID ARTERY ATHEROMA ( 9 FDA reports)
CATARACT CORTICAL ( 9 FDA reports)
CATHETER SITE HAEMORRHAGE ( 9 FDA reports)
CEREBRAL CYST ( 9 FDA reports)
CHEMOTHERAPY ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
COMPULSIVE SHOPPING ( 9 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 9 FDA reports)
DEAFNESS UNILATERAL ( 9 FDA reports)
DEFORMITY THORAX ( 9 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 9 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
DYSPONESIS ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
ELECTROCONVULSIVE THERAPY ( 9 FDA reports)
ELECTROLYTE DEPLETION ( 9 FDA reports)
ENCEPHALITIS VIRAL ( 9 FDA reports)
ENDOCARDIAL FIBROSIS ( 9 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 9 FDA reports)
EYE LASER SURGERY ( 9 FDA reports)
FEMORAL NECK FRACTURE ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 9 FDA reports)
FOETAL DISTRESS SYNDROME ( 9 FDA reports)
FOETAL HEART RATE ABNORMAL ( 9 FDA reports)
FORAMEN MAGNUM STENOSIS ( 9 FDA reports)
GALLBLADDER OPERATION ( 9 FDA reports)
GALLOP RHYTHM PRESENT ( 9 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 9 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 9 FDA reports)
GRIEF REACTION ( 9 FDA reports)
HAEMOGLOBIN ABNORMAL ( 9 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 9 FDA reports)
HIP DEFORMITY ( 9 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPOREFLEXIA ( 9 FDA reports)
INCISION SITE ERYTHEMA ( 9 FDA reports)
INCISION SITE OEDEMA ( 9 FDA reports)
INJECTION SITE CELLULITIS ( 9 FDA reports)
INJECTION SITE NODULE ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 9 FDA reports)
LIGAMENT DISORDER ( 9 FDA reports)
LIP DRY ( 9 FDA reports)
LIVER TRANSPLANT REJECTION ( 9 FDA reports)
LOOSE STOOLS ( 9 FDA reports)
MARITAL PROBLEM ( 9 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 9 FDA reports)
MEASLES ( 9 FDA reports)
MEGAKARYOCYTES DECREASED ( 9 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 9 FDA reports)
METASTASES TO PERITONEUM ( 9 FDA reports)
METASTATIC PAIN ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MUSCLE RUPTURE ( 9 FDA reports)
MYASTHENIA GRAVIS ( 9 FDA reports)
MYOCARDIAL FIBROSIS ( 9 FDA reports)
NASAL MUCOSAL DISORDER ( 9 FDA reports)
NASAL TURBINATE ABNORMALITY ( 9 FDA reports)
ONYCHOLYSIS ( 9 FDA reports)
OROANTRAL FISTULA ( 9 FDA reports)
PARACENTESIS ( 9 FDA reports)
PARATHYROID DISORDER ( 9 FDA reports)
PELVIC DISCOMFORT ( 9 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 9 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 9 FDA reports)
PNEUMONIA KLEBSIELLA ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POLYCYSTIC OVARIES ( 9 FDA reports)
POLYTRAUMATISM ( 9 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 9 FDA reports)
POSTOPERATIVE INFECTION ( 9 FDA reports)
PROCEDURAL HYPOTENSION ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 9 FDA reports)
QUADRIPARESIS ( 9 FDA reports)
RADIATION PNEUMONITIS ( 9 FDA reports)
RESPIRATORY TRACT IRRITATION ( 9 FDA reports)
RESUSCITATION ( 9 FDA reports)
RETINAL DETACHMENT ( 9 FDA reports)
SCAR EXCISION ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SENILE OSTEOPOROSIS ( 9 FDA reports)
SEPTIC EMBOLUS ( 9 FDA reports)
SKIN OEDEMA ( 9 FDA reports)
SLEEP TERROR ( 9 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 9 FDA reports)
STASIS DERMATITIS ( 9 FDA reports)
SUBDURAL HAEMORRHAGE ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 9 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 9 FDA reports)
URETHRAL STENOSIS ( 9 FDA reports)
UTERINE CANCER ( 9 FDA reports)
UTERINE FIBROSIS ( 9 FDA reports)
VENOOCCLUSIVE DISEASE ( 9 FDA reports)
VESTIBULAR NEURONITIS ( 9 FDA reports)
VOMITING PROJECTILE ( 9 FDA reports)
WEIGHT GAIN POOR ( 9 FDA reports)
WEST NILE VIRAL INFECTION ( 9 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 9 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SELF ESTEEM DECREASED ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SKIN HYPOPIGMENTATION ( 8 FDA reports)
SPUTUM PURULENT ( 8 FDA reports)
STENT REMOVAL ( 8 FDA reports)
SYSTEMIC MYCOSIS ( 8 FDA reports)
TETANY ( 8 FDA reports)
THORACOSTOMY ( 8 FDA reports)
THROMBOEMBOLIC STROKE ( 8 FDA reports)
TIC ( 8 FDA reports)
TONGUE DRY ( 8 FDA reports)
TOOTH RESORPTION ( 8 FDA reports)
URETERAL STENT INSERTION ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
VENOUS OCCLUSION ( 8 FDA reports)
VENOUS STENOSIS ( 8 FDA reports)
VERTEBRAL WEDGING ( 8 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 8 FDA reports)
VITAMIN B12 INCREASED ( 8 FDA reports)
VITAMIN C DEFICIENCY ( 8 FDA reports)
VOCAL CORD THICKENING ( 8 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 8 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 8 FDA reports)
WOUND HAEMORRHAGE ( 8 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 8 FDA reports)
ABNORMAL WEIGHT GAIN ( 8 FDA reports)
ACCIDENTAL DEATH ( 8 FDA reports)
ACETABULUM FRACTURE ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
ADNEXA UTERI CYST ( 8 FDA reports)
ALCOHOL DETOXIFICATION ( 8 FDA reports)
ANOXIA ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 8 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 8 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 8 FDA reports)
ASEPTIC NECROSIS BONE ( 8 FDA reports)
BACILLUS INFECTION ( 8 FDA reports)
BACTERIAL DISEASE CARRIER ( 8 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 8 FDA reports)
BIOPSY BONE ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 8 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 8 FDA reports)
BLOOD LACTIC ACID INCREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 8 FDA reports)
BONE INFARCTION ( 8 FDA reports)
BRAIN STEM INFARCTION ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREATH SOUNDS DECREASED ( 8 FDA reports)
CARBON DIOXIDE DECREASED ( 8 FDA reports)
CARDIAC PACEMAKER INSERTION ( 8 FDA reports)
CATHETER SITE ERYTHEMA ( 8 FDA reports)
CATHETER SITE RELATED REACTION ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 8 FDA reports)
CHAPPED LIPS ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CHEYNE-STOKES RESPIRATION ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 8 FDA reports)
CLOSED FRACTURE MANIPULATION ( 8 FDA reports)
COMMINUTED FRACTURE ( 8 FDA reports)
CORONARY ARTERY EMBOLISM ( 8 FDA reports)
CRYOTHERAPY ( 8 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DIABETES INSIPIDUS ( 8 FDA reports)
DIAPHRAGMATIC DISORDER ( 8 FDA reports)
DISINHIBITION ( 8 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 8 FDA reports)
ELEVATED MOOD ( 8 FDA reports)
ENDOCRINE DISORDER ( 8 FDA reports)
EPIDERMAL NECROSIS ( 8 FDA reports)
EXTRADURAL HAEMATOMA ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
EYE OEDEMA ( 8 FDA reports)
EYE ROLLING ( 8 FDA reports)
FEEDING DISORDER ( 8 FDA reports)
FOLATE DEFICIENCY ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
FULL BLOOD COUNT DECREASED ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GRIMACING ( 8 FDA reports)
HAEMOCHROMATOSIS ( 8 FDA reports)
HAEMODILUTION ( 8 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HEART TRANSPLANT ( 8 FDA reports)
HOSPICE CARE ( 8 FDA reports)
HYPERALDOSTERONISM ( 8 FDA reports)
HYPERCORTICOIDISM ( 8 FDA reports)
HYPOMETABOLISM ( 8 FDA reports)
IMPULSE-CONTROL DISORDER ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INSULIN RESISTANCE ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 8 FDA reports)
IRITIS ( 8 FDA reports)
JOINT ARTHROPLASTY ( 8 FDA reports)
KIDNEY MALROTATION ( 8 FDA reports)
LEGAL PROBLEM ( 8 FDA reports)
LESION EXCISION ( 8 FDA reports)
LIGAMENT INJURY ( 8 FDA reports)
LIMB OPERATION ( 8 FDA reports)
LIP BLISTER ( 8 FDA reports)
LOSS OF LIBIDO ( 8 FDA reports)
MACROGLOSSIA ( 8 FDA reports)
MADAROSIS ( 8 FDA reports)
MALLORY-WEISS SYNDROME ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 8 FDA reports)
METASTASES TO OVARY ( 8 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 8 FDA reports)
MOTION SICKNESS ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 8 FDA reports)
MYELOID LEUKAEMIA ( 8 FDA reports)
NARCOTIC INTOXICATION ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 8 FDA reports)
NEURODEGENERATIVE DISORDER ( 8 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 8 FDA reports)
NEUROMYOPATHY ( 8 FDA reports)
NEUTROPENIC COLITIS ( 8 FDA reports)
NIPPLE PAIN ( 8 FDA reports)
NODULE ON EXTREMITY ( 8 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 8 FDA reports)
OCULOGYRIC CRISIS ( 8 FDA reports)
OESOPHAGEAL CARCINOMA ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
ORAL PRURITUS ( 8 FDA reports)
ORTHOPEDIC PROCEDURE ( 8 FDA reports)
OSTECTOMY ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
PAINFUL RESPIRATION ( 8 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 8 FDA reports)
PAPILLOEDEMA ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PENILE OEDEMA ( 8 FDA reports)
PENIS DISORDER ( 8 FDA reports)
PERCUSSION TEST ABNORMAL ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PHLEBITIS SUPERFICIAL ( 8 FDA reports)
PITUITARY TUMOUR ( 8 FDA reports)
PLATELET TRANSFUSION ( 8 FDA reports)
POSITIVE ROMBERGISM ( 8 FDA reports)
POST PROCEDURAL NAUSEA ( 8 FDA reports)
PROCTITIS ( 8 FDA reports)
PROSTATISM ( 8 FDA reports)
PROSTHESIS IMPLANTATION ( 8 FDA reports)
PROTEUS INFECTION ( 8 FDA reports)
PROTRUSION TONGUE ( 8 FDA reports)
PSYCHOLOGICAL TRAUMA ( 8 FDA reports)
RADICULITIS BRACHIAL ( 8 FDA reports)
RECTAL FISSURE ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
RESPIRATORY ALKALOSIS ( 8 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ACUTE PSYCHOSIS ( 7 FDA reports)
ALCOHOLIC PANCREATITIS ( 7 FDA reports)
AMAUROSIS FUGAX ( 7 FDA reports)
AMINO ACID LEVEL INCREASED ( 7 FDA reports)
AMYLOIDOSIS ( 7 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
ANION GAP DECREASED ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
APICAL GRANULOMA ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
APPLICATION SITE PAIN ( 7 FDA reports)
APPLICATION SITE URTICARIA ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ARTERIOVENOUS MALFORMATION ( 7 FDA reports)
ASTERIXIS ( 7 FDA reports)
AUTISM ( 7 FDA reports)
BLADDER MASS ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 7 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 7 FDA reports)
BONE METABOLISM DISORDER ( 7 FDA reports)
BREAKTHROUGH PAIN ( 7 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 7 FDA reports)
BURNOUT SYNDROME ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 7 FDA reports)
CARBON DIOXIDE ABNORMAL ( 7 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 7 FDA reports)
CARDIOVERSION ( 7 FDA reports)
CATHETER SITE PAIN ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CHEST WALL OPERATION ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHONDROCALCINOSIS ( 7 FDA reports)
CHRONIC HEPATIC FAILURE ( 7 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DIET REFUSAL ( 7 FDA reports)
DRUG TOLERANCE INCREASED ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
DYSPNOEA EXACERBATED ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
ENTEROCELE ( 7 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 7 FDA reports)
EPHELIDES ( 7 FDA reports)
ESCHERICHIA TEST POSITIVE ( 7 FDA reports)
EUSTACHIAN TUBE DISORDER ( 7 FDA reports)
EUSTACHIAN TUBE PATULOUS ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
EXPLORATORY OPERATION ( 7 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 7 FDA reports)
EYE INFECTION VIRAL ( 7 FDA reports)
FEELING GUILTY ( 7 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 7 FDA reports)
GASTRIC BYPASS ( 7 FDA reports)
GASTRIC INFECTION ( 7 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 7 FDA reports)
GASTROINTESTINAL TOXICITY ( 7 FDA reports)
GRUNTING ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HELICOBACTER GASTRITIS ( 7 FDA reports)
HEPATIC TRAUMA ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HOMICIDE ( 7 FDA reports)
HORNER'S SYNDROME ( 7 FDA reports)
HYDROPNEUMOTHORAX ( 7 FDA reports)
HYPERMAGNESAEMIA ( 7 FDA reports)
HYPERPROLACTINAEMIA ( 7 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
ILIAC ARTERY OCCLUSION ( 7 FDA reports)
ILIAC ARTERY STENOSIS ( 7 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 7 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 7 FDA reports)
INJECTION SITE ANAESTHESIA ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INJECTION SITE INFLAMMATION ( 7 FDA reports)
INTESTINAL STENOSIS ( 7 FDA reports)
IRIDOCYCLITIS ( 7 FDA reports)
JOINT DESTRUCTION ( 7 FDA reports)
KIDNEY FIBROSIS ( 7 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 7 FDA reports)
LIBIDO INCREASED ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
LIPODYSTROPHY ACQUIRED ( 7 FDA reports)
LITHOTRIPSY ( 7 FDA reports)
LIVER TRANSPLANT ( 7 FDA reports)
MAMMARY DUCT ECTASIA ( 7 FDA reports)
MANDIBULAR PROSTHESIS USER ( 7 FDA reports)
METASTASES TO ADRENALS ( 7 FDA reports)
METASTASES TO MUSCLE ( 7 FDA reports)
MIXED HYPERLIPIDAEMIA ( 7 FDA reports)
MONOPLEGIA ( 7 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
NUCHAL RIGIDITY ( 7 FDA reports)
OPTIC NERVE CUPPING ( 7 FDA reports)
ORAL DYSAESTHESIA ( 7 FDA reports)
ORAL MUCOSAL BLISTERING ( 7 FDA reports)
ORGANISING PNEUMONIA ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
PAIN EXACERBATED ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PARADOXICAL DRUG REACTION ( 7 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 7 FDA reports)
PEAU D'ORANGE ( 7 FDA reports)
PERIODONTAL OPERATION ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 7 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 7 FDA reports)
PLATELET COUNT ABNORMAL ( 7 FDA reports)
PNEUMOPERITONEUM ( 7 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 7 FDA reports)
POST PROCEDURAL DIARRHOEA ( 7 FDA reports)
PRESSURE OF SPEECH ( 7 FDA reports)
PRODUCT TASTE ABNORMAL ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 7 FDA reports)
READING DISORDER ( 7 FDA reports)
RENAL CANCER METASTATIC ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RENAL INFARCT ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 7 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 7 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 7 FDA reports)
SALPINGO-OOPHORECTOMY ( 7 FDA reports)
SECONDARY SEQUESTRUM ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SKIN CHAPPED ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SPINAL CORD INJURY ( 7 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 7 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
TERMINAL STATE ( 7 FDA reports)
THROMBOCYTHAEMIA ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
TRAUMATIC HAEMATOMA ( 7 FDA reports)
TUBERCULIN TEST POSITIVE ( 7 FDA reports)
ULCER HAEMORRHAGE ( 7 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
URINE FLOW DECREASED ( 7 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
XEROSIS ( 7 FDA reports)
RHEUMATIC FEVER ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
SEPTOPLASTY ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SKIN CANDIDA ( 6 FDA reports)
SLEEP WALKING ( 6 FDA reports)
SLOW RESPONSE TO STIMULI ( 6 FDA reports)
SPINAL CLAUDICATION ( 6 FDA reports)
SPIROMETRY ABNORMAL ( 6 FDA reports)
SPLENIC CYST ( 6 FDA reports)
SPLENIC INJURY ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
SPUTUM DECREASED ( 6 FDA reports)
STENT OCCLUSION ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
STRABISMUS ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
THYROIDECTOMY ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRACHEAL OPERATION ( 6 FDA reports)
TRACHEITIS ( 6 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
URINE OUTPUT INCREASED ( 6 FDA reports)
UTERINE DISORDER ( 6 FDA reports)
UTERINE MASS ( 6 FDA reports)
VAGINAL LESION ( 6 FDA reports)
VASCULAR GRAFT OCCLUSION ( 6 FDA reports)
VOCAL CORD ATROPHY ( 6 FDA reports)
WISDOM TEETH REMOVAL ( 6 FDA reports)
YAWNING ( 6 FDA reports)
ABDOMINAL RIGIDITY ( 6 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ABSCESS LIMB ( 6 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANGIOGRAM ABNORMAL ( 6 FDA reports)
AORTIC VALVE CALCIFICATION ( 6 FDA reports)
AORTIC VALVE REPLACEMENT ( 6 FDA reports)
APPLICATION SITE DISCOMFORT ( 6 FDA reports)
APPLICATION SITE VESICLES ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 6 FDA reports)
ARTHROPOD BITE ( 6 FDA reports)
ASPERGER'S DISORDER ( 6 FDA reports)
AUTONOMIC NEUROPATHY ( 6 FDA reports)
AXILLARY VEIN THROMBOSIS ( 6 FDA reports)
BIPOLAR II DISORDER ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD CREATININE ABNORMAL ( 6 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 6 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 6 FDA reports)
BLOOD OESTROGEN DECREASED ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BRAIN STEM SYNDROME ( 6 FDA reports)
BREAST HAEMATOMA ( 6 FDA reports)
BRONCHIAL DISORDER ( 6 FDA reports)
BRONCHIAL NEOPLASM ( 6 FDA reports)
BRONCHIAL SECRETION RETENTION ( 6 FDA reports)
CARDIORENAL SYNDROME ( 6 FDA reports)
CAROTID ARTERY ANEURYSM ( 6 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 6 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
CIRRHOSIS ALCOHOLIC ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
COMPULSIONS ( 6 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 6 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 6 FDA reports)
CORNEAL OPACITY ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CULTURE STOOL POSITIVE ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 6 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DEATH OF RELATIVE ( 6 FDA reports)
DELUSIONAL PERCEPTION ( 6 FDA reports)
DERMATILLOMANIA ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 6 FDA reports)
EJACULATION FAILURE ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 6 FDA reports)
EYE BURNS ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 6 FDA reports)
FAT TISSUE INCREASED ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FEELING OF RELAXATION ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
FUNGAEMIA ( 6 FDA reports)
GASTROINTESTINAL ULCER ( 6 FDA reports)
GIANT CELL EPULIS ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
GRANULOCYTES MATURATION ARREST ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HAEMOGLOBINURIA ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HAEMORRHAGIC DIATHESIS ( 6 FDA reports)
HAND DEFORMITY ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 6 FDA reports)
HOARSENESS ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 6 FDA reports)
INTESTINAL FISTULA ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
KETONURIA ( 6 FDA reports)
LATEX ALLERGY ( 6 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEUKAEMIA PLASMACYTIC ( 6 FDA reports)
LEUKOSTASIS ( 6 FDA reports)
LIPIDS INCREASED ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 6 FDA reports)
MEAN CELL VOLUME DECREASED ( 6 FDA reports)
MEAN CELL VOLUME INCREASED ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
MEGACOLON ( 6 FDA reports)
MENINGIOMA BENIGN ( 6 FDA reports)
MITRAL VALVE STENOSIS ( 6 FDA reports)
MONOCLONAL GAMMOPATHY ( 6 FDA reports)
NAIL DISCOLOURATION ( 6 FDA reports)
NEONATAL DISORDER ( 6 FDA reports)
NERVE BLOCK ( 6 FDA reports)
NEUROPATHIC ARTHROPATHY ( 6 FDA reports)
OBSTRUCTION GASTRIC ( 6 FDA reports)
OESOPHAGEAL INFECTION ( 6 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 6 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 6 FDA reports)
PANCREATITIS RELAPSING ( 6 FDA reports)
PARAKERATOSIS ( 6 FDA reports)
PEDAL PULSE DECREASED ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PENILE PAIN ( 6 FDA reports)
PERITONEAL LESION ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PLATELET DISORDER ( 6 FDA reports)
PLATELET PRODUCTION DECREASED ( 6 FDA reports)
PLEURAL DISORDER ( 6 FDA reports)
PNEUMATOSIS INTESTINALIS ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
POISONING ( 6 FDA reports)
POLYMYALGIA RHEUMATICA ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
POST POLIO SYNDROME ( 6 FDA reports)
POST PROCEDURAL VOMITING ( 6 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 6 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 6 FDA reports)
POSTURING ( 6 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 6 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
PSYCHOSOMATIC DISEASE ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 6 FDA reports)
REBOUND EFFECT ( 6 FDA reports)
RECTAL ABSCESS ( 6 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 6 FDA reports)
RENAL HAEMORRHAGE ( 6 FDA reports)
REPETITIVE SPEECH ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 6 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 5 FDA reports)
ACETONAEMIA ( 5 FDA reports)
ADHESION ( 5 FDA reports)
AGITATION NEONATAL ( 5 FDA reports)
ANAL SPHINCTER ATONY ( 5 FDA reports)
ANDROGEN DEFICIENCY ( 5 FDA reports)
ANORGASMIA ( 5 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 5 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 5 FDA reports)
AORTIC BYPASS ( 5 FDA reports)
APPLICATION SITE BLEEDING ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ARTERIAL STENT INSERTION ( 5 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 5 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 5 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 5 FDA reports)
AURICULAR SWELLING ( 5 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 5 FDA reports)
AXILLARY PAIN ( 5 FDA reports)
BELLIGERENCE ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD CALCIUM ABNORMAL ( 5 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 5 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 5 FDA reports)
BLOOD GASES ABNORMAL ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BODY TINEA ( 5 FDA reports)
BONE CANCER METASTATIC ( 5 FDA reports)
BRADYKINESIA ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BULBAR PALSY ( 5 FDA reports)
BURN DRESSING ( 5 FDA reports)
CALCULUS BLADDER ( 5 FDA reports)
CANDIDA SEPSIS ( 5 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 5 FDA reports)
CARTILAGE INJURY ( 5 FDA reports)
CATARACT SUBCAPSULAR ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHEST TUBE INSERTION ( 5 FDA reports)
CHONDROPATHY ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
COAGULATION TIME PROLONGED ( 5 FDA reports)
COCCYDYNIA ( 5 FDA reports)
COLON CANCER STAGE III ( 5 FDA reports)
COLONIC FISTULA ( 5 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
COR PULMONALE CHRONIC ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DEMENTIA WITH LEWY BODIES ( 5 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 5 FDA reports)
DIABETIC VASCULAR DISORDER ( 5 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 5 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DRY GANGRENE ( 5 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 5 FDA reports)
DYSPLASTIC NAEVUS ( 5 FDA reports)
EARLY SATIETY ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 5 FDA reports)
FAILURE OF IMPLANT ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FOOD AVERSION ( 5 FDA reports)
FOOT OPERATION ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
GANGLION ( 5 FDA reports)
GASTRIC CANCER ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GLIOBLASTOMA MULTIFORME ( 5 FDA reports)
HAEMANGIOMA OF SKIN ( 5 FDA reports)
HEPATITIS ALCOHOLIC ( 5 FDA reports)
HORMONE LEVEL ABNORMAL ( 5 FDA reports)
HYPERCHLORHYDRIA ( 5 FDA reports)
HYPERKINETIC HEART SYNDROME ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 5 FDA reports)
HYPERTONIA ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
ILEAL STENOSIS ( 5 FDA reports)
ILIAC ARTERY THROMBOSIS ( 5 FDA reports)
ILIUM FRACTURE ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INGUINAL MASS ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTESTINAL MASS ( 5 FDA reports)
INTUSSUSCEPTION ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JEJUNAL ULCER ( 5 FDA reports)
JOINT HYPEREXTENSION ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
LIGAMENT PAIN ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
LIP INJURY ( 5 FDA reports)
LYMPH NODE CALCIFICATION ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MEDIASTINAL HAEMATOMA ( 5 FDA reports)
METASTASES TO NECK ( 5 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
MOLE EXCISION ( 5 FDA reports)
MURDER ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
NASAL FLARING ( 5 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 5 FDA reports)
NEUROGENIC BOWEL ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 5 FDA reports)
ORTHOSTATIC INTOLERANCE ( 5 FDA reports)
OVARIAN CANCER METASTATIC ( 5 FDA reports)
OVARIAN DISORDER ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PERINEAL ABSCESS ( 5 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 5 FDA reports)
PERITONEAL DIALYSIS ( 5 FDA reports)
PEYRONIE'S DISEASE ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 5 FDA reports)
PHARYNGEAL MASS ( 5 FDA reports)
PIRIFORMIS SYNDROME ( 5 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 5 FDA reports)
PNEUMOCONIOSIS ( 5 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PROLONGED PREGNANCY ( 5 FDA reports)
PROSTATE CANCER METASTATIC ( 5 FDA reports)
PROSTATIC CALCIFICATION ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
PULMONARY CALCIFICATION ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PYODERMA ( 5 FDA reports)
RADIATION NECROSIS ( 5 FDA reports)
RADIATION NEUROPATHY ( 5 FDA reports)
RECALL PHENOMENON ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
RED BLOOD CELLS URINE ( 5 FDA reports)
RED MAN SYNDROME ( 5 FDA reports)
RETINAL ARTERY OCCLUSION ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
SARCOMA ( 5 FDA reports)
SENILE DEMENTIA ( 5 FDA reports)
SENSATION OF BLOOD FLOW ( 5 FDA reports)
SEROSITIS ( 5 FDA reports)
SHOPLIFTING ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SKIN LESION EXCISION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SMOKER ( 5 FDA reports)
SOCIAL PHOBIA ( 5 FDA reports)
SOLILOQUY ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
SUBACUTE ENDOCARDITIS ( 5 FDA reports)
SUPERINFECTION BACTERIAL ( 5 FDA reports)
SUPRAPUBIC PAIN ( 5 FDA reports)
SYNOVIAL DISORDER ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
TACHYCARDIA PAROXYSMAL ( 5 FDA reports)
THEFT ( 5 FDA reports)
TINEL'S SIGN ( 5 FDA reports)
TORTICOLLIS ( 5 FDA reports)
TOXIC OPTIC NEUROPATHY ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 5 FDA reports)
TRICHORRHEXIS ( 5 FDA reports)
TROPONIN T INCREASED ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
UMBILICAL HERNIA REPAIR ( 5 FDA reports)
URETHRAL PAIN ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
UVULECTOMY ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VESTIBULOPLASTY ( 5 FDA reports)
VIRAL RASH ( 5 FDA reports)
VULVAL DISORDER ( 5 FDA reports)
WHITE BLOOD CELL COUNT ( 5 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SARCOMA OF SKIN ( 4 FDA reports)
SCAN BONE MARROW ABNORMAL ( 4 FDA reports)
SCIATIC NERVE INJURY ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SERUM SEROTONIN INCREASED ( 4 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 4 FDA reports)
SINUS ANTROSTOMY ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SLEEP TALKING ( 4 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 4 FDA reports)
SMALL INTESTINAL STENOSIS ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPIDER VEIN ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
SPONTANEOUS PENILE ERECTION ( 4 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 4 FDA reports)
SUBRETINAL FIBROSIS ( 4 FDA reports)
SUSPICIOUSNESS ( 4 FDA reports)
SYMBOLIC DYSFUNCTION ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 4 FDA reports)
THERAPY CESSATION ( 4 FDA reports)
THROMBOANGIITIS OBLITERANS ( 4 FDA reports)
THYROID CANCER METASTATIC ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TOOTH MALFORMATION ( 4 FDA reports)
TOXIC NEUROPATHY ( 4 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 4 FDA reports)
TRACHEOMALACIA ( 4 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
UTERINE ATROPHY ( 4 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 4 FDA reports)
VAGINAL MYCOSIS ( 4 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VICTIM OF CRIME ( 4 FDA reports)
VITREOUS DEGENERATION ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WEANING FAILURE ( 4 FDA reports)
WHITE BLOOD CELL DISORDER ( 4 FDA reports)
WOUND CLOSURE ( 4 FDA reports)
WOUND NECROSIS ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACCOMMODATION DISORDER ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 4 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 4 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 4 FDA reports)
ACUTE STRESS DISORDER ( 4 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 4 FDA reports)
ADRENAL CARCINOMA ( 4 FDA reports)
ADRENAL NEOPLASM ( 4 FDA reports)
ADVERSE REACTION ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
ANORECTAL OPERATION ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 4 FDA reports)
AORTIC EMBOLUS ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
APHAKIA ( 4 FDA reports)
APNOEIC ATTACK ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTERIOVENOUS FISTULA ( 4 FDA reports)
ARTHRODESIS ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATRIAL THROMBOSIS ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BASOPHIL COUNT INCREASED ( 4 FDA reports)
BENIGN BONE NEOPLASM ( 4 FDA reports)
BIOPSY LUNG ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLADDER NEOPLASM ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLEEDING TIME ABNORMAL ( 4 FDA reports)
BLINDNESS CORTICAL ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 4 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
BLUE TOE SYNDROME ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BORDERLINE GLAUCOMA ( 4 FDA reports)
BREAST CELLULITIS ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
CARBON MONOXIDE POISONING ( 4 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 4 FDA reports)
CARDIAC ABLATION ( 4 FDA reports)
CARDIAC PACEMAKER REVISION ( 4 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CERVICITIS ( 4 FDA reports)
CERVIX INFLAMMATION ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHONDROPLASTY ( 4 FDA reports)
CLEFT LIP ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 4 FDA reports)
COGWHEEL RIGIDITY ( 4 FDA reports)
COLD AGGLUTININS ( 4 FDA reports)
CONFUSION POSTOPERATIVE ( 4 FDA reports)
CONJUNCTIVAL ABRASION ( 4 FDA reports)
CONJUNCTIVAL CYST ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
CORONARY ANGIOPLASTY ( 4 FDA reports)
CRANIAL NEUROPATHY ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DELAYED ENGRAFTMENT ( 4 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DENTAL PROSTHESIS USER ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DEVICE INEFFECTIVE ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 4 FDA reports)
DRUG DETOXIFICATION ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
EAR PRURITUS ( 4 FDA reports)
ECTOPIC PREGNANCY ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EPISCLERITIS ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ETHMOID SINUS SURGERY ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EYE INJURY ( 4 FDA reports)
EYES SUNKEN ( 4 FDA reports)
FACTOR XI DEFICIENCY ( 4 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FRACTURED COCCYX ( 4 FDA reports)
GALLBLADDER PAIN ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GASTROENTERITIS SALMONELLA ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 4 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 4 FDA reports)
GENERAL NUTRITION DISORDER ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GENITAL RASH ( 4 FDA reports)
GERSTMANN'S SYNDROME ( 4 FDA reports)
GLOMERULONEPHRITIS ( 4 FDA reports)
GLOMERULOSCLEROSIS ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
GROIN ABSCESS ( 4 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAIR COLOUR CHANGES ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEART VALVE REPLACEMENT ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HY'S LAW CASE ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERCREATININAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 4 FDA reports)
HYPOCOMPLEMENTAEMIA ( 4 FDA reports)
HYPOGLYCAEMIC COMA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOMENORRHOEA ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
ILEITIS ( 4 FDA reports)
IMPAIRED FASTING GLUCOSE ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFUSION SITE INFECTION ( 4 FDA reports)
INFUSION SITE WARMTH ( 4 FDA reports)
INGUINAL HERNIA REPAIR ( 4 FDA reports)
INJECTION SITE BURNING ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE PAPULE ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
INTRAPERICARDIAL THROMBOSIS ( 4 FDA reports)
JAW CYST ( 4 FDA reports)
KNEE DEFORMITY ( 4 FDA reports)
LAZINESS ( 4 FDA reports)
LDL/HDL RATIO ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LIMB ASYMMETRY ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LIVIDITY ( 4 FDA reports)
LOCKED-IN SYNDROME ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MENINGEAL DISORDER ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
MENTAL DISABILITY ( 4 FDA reports)
METASTASES TO BONE MARROW ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
MICROALBUMINURIA ( 4 FDA reports)
MILIA ( 4 FDA reports)
MINERAL METABOLISM DISORDER ( 4 FDA reports)
MOANING ( 4 FDA reports)
MONOPARESIS ( 4 FDA reports)
MORBID THOUGHTS ( 4 FDA reports)
MUCOUS STOOLS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
NASAL SEPTAL OPERATION ( 4 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 4 FDA reports)
NEUTROPHIL COUNT ( 4 FDA reports)
OCULAR NEOPLASM ( 4 FDA reports)
OESOPHAGEAL DILATATION ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
PANCREATIC MASS ( 4 FDA reports)
PANNICULITIS ( 4 FDA reports)
PARACENTESIS ABDOMEN ( 4 FDA reports)
PARANASAL CYST ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PARKINSONIAN REST TREMOR ( 4 FDA reports)
PAROTID DUCT OBSTRUCTION ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PERICARDIAL CYST ( 4 FDA reports)
PERIODONTAL INFECTION ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 4 FDA reports)
PLEURAL NEOPLASM ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 4 FDA reports)
POLYCHROMASIA ( 4 FDA reports)
POLYCYTHAEMIA VERA ( 4 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 4 FDA reports)
PROSTATIC DISORDER ( 4 FDA reports)
PROTEIN URINE ( 4 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PSEUDOCYST ( 4 FDA reports)
PSEUDODEMENTIA ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
RENAL ARTERIOSCLEROSIS ( 4 FDA reports)
RETINAL DISORDER ( 4 FDA reports)
ABSCESS OF EYELID ( 3 FDA reports)
ACANTHOSIS ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ALLERGY TEST POSITIVE ( 3 FDA reports)
ALLODYNIA ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
ALOPECIA UNIVERSALIS ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 3 FDA reports)
ANDROGENS DECREASED ( 3 FDA reports)
ANGIOFIBROMA ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT TOXICITY ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
AORTIC BRUIT ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 3 FDA reports)
ASTROCYTOMA ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BACTERIAL TEST NEGATIVE ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILE DUCT STENT INSERTION ( 3 FDA reports)
BILOMA ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIOPSY LIVER ABNORMAL ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BONE ABSCESS ( 3 FDA reports)
BOTULISM ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
BREAST CANCER STAGE IV ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CALCIPHYLAXIS ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CHALAZION ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHEST WALL CYST ( 3 FDA reports)
CHEST WALL NECROSIS ( 3 FDA reports)
CHOLANGITIS SCLEROSING ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 3 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONGENITAL BLADDER ANOMALY ( 3 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 3 FDA reports)
CONVULSION NEONATAL ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
CYCLIC NEUTROPENIA ( 3 FDA reports)
CYCLIC VOMITING SYNDROME ( 3 FDA reports)
CYST REMOVAL ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
CYTOKINE RELEASE SYNDROME ( 3 FDA reports)
DEJA VU ( 3 FDA reports)
DELUSION OF REFERENCE ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE MIGRATION ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 3 FDA reports)
DIABETIC ENTEROPATHY ( 3 FDA reports)
DIABETIC GASTROENTEROPATHY ( 3 FDA reports)
DIABETIC GASTROPATHY ( 3 FDA reports)
DIARRHOEA NEONATAL ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DIZZINESS EXERTIONAL ( 3 FDA reports)
DRUG ADDICT ( 3 FDA reports)
DRUG DIVERSION ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
ECHOCARDIOGRAM ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
ELECTRIC SHOCK ( 3 FDA reports)
ENDARTERECTOMY ( 3 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 3 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 3 FDA reports)
ENTERITIS INFECTIOUS ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
EX-TOBACCO USER ( 3 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
EYELID PAIN ( 3 FDA reports)
FACTITIOUS DISORDER ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FEMORAL HERNIA ( 3 FDA reports)
FIBRIN INCREASED ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FOREIGN BODY ASPIRATION ( 3 FDA reports)
FRACTURE TREATMENT ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GASTRECTOMY ( 3 FDA reports)
GASTRIC PH DECREASED ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 3 FDA reports)
GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
GASTROOESOPHAGITIS ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENERAL SYMPTOM ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
GROIN INFECTION ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HAEMOSIDEROSIS ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATIC CANCER METASTATIC ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC PAIN ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATOBILIARY DISEASE ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
ICHTHYOSIS ACQUIRED ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 3 FDA reports)
INBORN ERROR OF METABOLISM ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCISIONAL HERNIA REPAIR ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 3 FDA reports)
INJECTION SITE PUSTULE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
JOINT LOCK ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LACRIMAL DISORDER ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LARYNGEAL STENOSIS ( 3 FDA reports)
LASER THERAPY ( 3 FDA reports)
LDL/HDL RATIO INCREASED ( 3 FDA reports)
LENTICULAR OPACITIES ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LIVER SCAN ABNORMAL ( 3 FDA reports)
LOCAL REACTION ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOSS OF PROPRIOCEPTION ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
MACULAR HOLE ( 3 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 3 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 3 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 3 FDA reports)
MALIGNANT TUMOUR EXCISION ( 3 FDA reports)
MANDIBULECTOMY ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MARCHIAFAVA-BIGNAMI DISEASE ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 3 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MEIBOMIANITIS ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENINGOCELE ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
MESOTHELIOMA MALIGNANT ( 3 FDA reports)
METASTASES TO BLADDER ( 3 FDA reports)
METASTASES TO CHEST WALL ( 3 FDA reports)
METASTASES TO PANCREAS ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MICTURITION FREQUENCY DECREASED ( 3 FDA reports)
MITRAL VALVE DISEASE MIXED ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYELOMALACIA ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NECROTISING FASCIITIS ( 3 FDA reports)
NEONATAL TACHYPNOEA ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OEDEMA GENITAL ( 3 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL POLYP ( 3 FDA reports)
OMENTUM NEOPLASM ( 3 FDA reports)
OOPHORECTOMY BILATERAL ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
OROMANDIBULAR DYSTONIA ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
ORTHOSTATIC HYPERTENSION ( 3 FDA reports)
OSTEOMYELITIS DRAINAGE ( 3 FDA reports)
OSTEOPETROSIS ( 3 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OTOTOXICITY ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
PANCOAST'S TUMOUR ( 3 FDA reports)
PANCREATIC DUCT DILATATION ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PARADOXICAL EMBOLISM ( 3 FDA reports)
PELVIC MASS ( 3 FDA reports)
PERINEURIAL CYST ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONEAL INFECTION ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PHYSIOTHERAPY ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PINGUECULA ( 3 FDA reports)
PLAGUE ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA ESCHERICHIA ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POSTOPERATIVE ABSCESS ( 3 FDA reports)
POSTPARTUM DISORDER ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRECANCEROUS CELLS PRESENT ( 3 FDA reports)
PRESBYACUSIS ( 3 FDA reports)
PRESENILE DEMENTIA ( 3 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PRODUCT SIZE ISSUE ( 3 FDA reports)
PRODUCT TAMPERING ( 3 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 3 FDA reports)
PSEUDARTHROSIS ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOTIC BEHAVIOUR ( 3 FDA reports)
PUBIC RAMI FRACTURE ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RADIAL NERVE PALSY ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 3 FDA reports)
RASH FOLLICULAR ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
REGURGITATION OF FOOD ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
REPETITIVE STRAIN INJURY ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RETROGRADE EJACULATION ( 3 FDA reports)
RHINITIS PERENNIAL ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SALPINGECTOMY ( 3 FDA reports)
SCAN LYMPH NODES ( 3 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 3 FDA reports)
SCROTAL SWELLING ( 3 FDA reports)
SEBACEOUS ADENOMA ( 3 FDA reports)
SEMEN VOLUME DECREASED ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SKIN GRAFT ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLEEP-RELATED EATING DISORDER ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SOMNOLENCE NEONATAL ( 3 FDA reports)
SPINAL CORD DISORDER ( 3 FDA reports)
SPINAL DECOMPRESSION ( 3 FDA reports)
SPONDYLOARTHROPATHY ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STOOL ANALYSIS ABNORMAL ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TENDINOUS CONTRACTURE ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOLYSIS ( 3 FDA reports)
TINEA CRURIS ( 3 FDA reports)
TOE OPERATION ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TONSILLAR INFLAMMATION ( 3 FDA reports)
TRAUMATIC LIVER INJURY ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TREMOR NEONATAL ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
URETERIC OPERATION ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINE ANALYSIS ( 3 FDA reports)
UTERINE DILATION AND CURETTAGE ( 3 FDA reports)
VASCULAR INJURY ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULAR SHUNT ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VIRAL SINUSITIS ( 3 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
VULVOVAGINAL ERYTHEMA ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WEIGHT ABNORMAL ( 3 FDA reports)
WHIPLASH INJURY ( 3 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RICKETS ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALMONELLA BACTERAEMIA ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCHOOL REFUSAL ( 2 FDA reports)
SCLERAL OEDEMA ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SEIZURE ANOXIC ( 2 FDA reports)
SERRATIA BACTERAEMIA ( 2 FDA reports)
SEXUAL ACTIVITY INCREASED ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN ULCER HAEMORRHAGE ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOCIAL FEAR ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPERM CONCENTRATION ZERO ( 2 FDA reports)
SPINAL CORD INJURY CERVICAL ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPINAL OPERATION ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC INFECTION ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLITIC MYELOPATHY ( 2 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 2 FDA reports)
SPOUSAL ABUSE ( 2 FDA reports)
STAB WOUND ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SUTURE REMOVAL ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TACHYCARDIA FOETAL ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THYROIDITIS CHRONIC ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 2 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
TUMOUR LOCAL INVASION ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TYPHOID FEVER ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
URINARY BLADDER RUPTURE ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
URINE CYTOLOGY ABNORMAL ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE ENLARGEMENT ( 2 FDA reports)
UTERINE MALPOSITION ( 2 FDA reports)
UTERINE OPERATION ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR GRAFT ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VENOUS LAKE ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR DRAINAGE ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VICTIM OF HOMICIDE ( 2 FDA reports)
VICTIM OF SEXUAL ABUSE ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WALLENBERG SYNDROME ( 2 FDA reports)
WHITE BLOOD CELL AGGLUTINATION PRESENT ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND EVISCERATION ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALLERGIC OEDEMA ( 2 FDA reports)
ALLERGIC SINUSITIS ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKLE RECONSTRUCTION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
ARCUS LIPOIDES ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 2 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BILE OUTPUT ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 2 FDA reports)
BIOPSY PROSTATE ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLAST CELLS ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BLOOD URIC ACID ABNORMAL ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRANCHIAL CYST ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BROW PRESENTATION ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL CALCIFICATION ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CERVICAL CONISATION ( 2 FDA reports)
CERVIX CARCINOMA RECURRENT ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CHONDROMATOSIS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
CONDUCT DISORDER ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL PNEUMONIA ( 2 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 2 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
CRANIOSYNOSTOSIS ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CYP2D6 POLYMORPHISM ( 2 FDA reports)
CYSTOPEXY ( 2 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DEAFNESS TRAUMATIC ( 2 FDA reports)
DEATH OF PET ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DIVERTICULUM DUODENAL ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG NAME CONFUSION ( 2 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 2 FDA reports)
DUODENAL STENOSIS ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
EBSTEIN'S ANOMALY ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC KIDNEY ( 2 FDA reports)
ELDER ABUSE ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
ENDOCARDITIS CANDIDA ( 2 FDA reports)
ENDOLYMPHATIC HYDROPS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROBACTER SEPSIS ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHAR ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FALLOPIAN TUBE DISORDER ( 2 FDA reports)
FALLOPIAN TUBE PERFORATION ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING PROBLEM IN CHILD ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
FLUOROSIS ( 2 FDA reports)
FOETAL CYSTIC HYGROMA ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER CONGENITAL ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 2 FDA reports)
GASTROSTOMY ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC ARTERY OCCLUSION ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HIP SWELLING ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HOUSE DUST ALLERGY ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERINSULINISM ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOTHERMIA NEONATAL ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
ILEOCOLECTOMY ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 2 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INJECTION SITE DERMATITIS ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 2 FDA reports)
INTESTINAL STOMA COMPLICATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRAOCULAR MELANOMA ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
JOINT SURGERY ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KYPHOSIS CONGENITAL ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARGE INTESTINAL STRICTURE ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LICHEN MYXOEDEMATOSUS ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOMA OF BREAST ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER CARCINOMA RUPTURED ( 2 FDA reports)
LIVER FUNCTION TEST ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LOSS OF DREAMING ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LYMPHATIC OBSTRUCTION ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 2 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MICROCYTOSIS ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE ENZYME INCREASED ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
MYOSITIS OSSIFICANS ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOVASCULARISATION ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 2 FDA reports)
NUCLEATED RED CELLS ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OCULAR CANCER METASTATIC ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 2 FDA reports)
OESOPHAGEAL OEDEMA ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
ONYCHOPHAGIA ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC DISC DRUSEN ( 2 FDA reports)
ORBITAL INFECTION ( 2 FDA reports)
OSTEOCHONDRITIS ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OSTEOTOMY ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OVARIAN RUPTURE ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PASSIVE SMOKING ( 2 FDA reports)
PCO2 ABNORMAL ( 2 FDA reports)
PELVIC HAEMATOMA ( 2 FDA reports)
PELVIC INFECTION ( 2 FDA reports)
PELVIC NEOPLASM ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PH URINE INCREASED ( 2 FDA reports)
PHARYNGEAL CANDIDIASIS ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHLEBOSCLEROSIS ( 2 FDA reports)
PHONOLOGICAL DISORDER ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL DECORTICATION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
POOR SUCKING REFLEX ( 2 FDA reports)
POST CONCUSSION SYNDROME ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POSTPARTUM DEPRESSION ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRECOCIOUS PUBERTY ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATIC ABSCESS ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PSYCHOPATHIC PERSONALITY ( 2 FDA reports)
PTERYGIUM ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
RASH SCALY ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
RECTAL ADENOMA ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL BURR CELLS PRESENT ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RENAL ANEURYSM ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RETINAL ISCHAEMIA ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 2 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 2 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGY TO VACCINE ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN ABNORMAL ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMAUROTIC FAMILIAL IDIOCY ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANALGESIC DRUG LEVEL ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANEURYSMAL BONE CYST ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANORECTAL AGENESIS ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE DISCHARGE ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOGRAM CORONARY NORMAL ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASBESTOSIS ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASTROCYTOMA MALIGNANT ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AUTOPHOBIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY FIBROSIS ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY TONGUE ABNORMAL ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER INJURY ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ( 1 FDA reports)
BLOOD ETHANOL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD SODIUM ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THROMBIN ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER, WITH POSTPARTUM ONSET ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURKHOLDERIA TEST POSITIVE ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURN OF INTERNAL ORGANS ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOCARCINOMA ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 4 ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER RECURRENT ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL MEGACOLON ( 1 FDA reports)
CONGENITAL PANCREATIC ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
COWS MILK FREE DIET ( 1 FDA reports)
CRANIAL NERVE INJURY ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTIC LYMPHANGIOMA ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DESMOID TUMOUR ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC DERMOPATHY ( 1 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIET NONCOMPLIANCE ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELASTOSIS PERFORANS ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
EMOTIONAL POVERTY ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPENDYMOMA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FALSE POSITIVE TUBERCULOSIS TEST ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAIR DYE USER ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CALCIFICATION ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HOFFMANN'S SIGN ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HUMAN ANTICHIMERIC ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 1 FDA reports)
HYDROCELE OPERATION ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE EROSION ( 1 FDA reports)
IMPLANT SITE RASH ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW OSTEITIS ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KARNOFSKY SCALE WORSENED ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARYNGEAL OPERATION ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPASE URINE INCREASED ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALE ORGASMIC DISORDER ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 1 FDA reports)
MALOCCLUSION ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM INCREASED ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGIOMA SURGERY ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA MALIGNANT RECURRENT ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO MOUTH ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METHAEMOGLOBINURIA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUCOSAL NECROSIS ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL BED DISORDER ( 1 FDA reports)
NAIL BED TENDERNESS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NERVE ROOT INJURY LUMBAR ( 1 FDA reports)
NEURILEMMOMA MALIGNANT ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NIPPLE EXUDATE BLOODY ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOSOPHOBIA ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSTRUCTED LABOUR ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC TRACT GLIOMA ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OTOSALPINGITIS ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVERWORK ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PAIN TRAUMA ACTIVATED ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS DIVISUM ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC INJURY ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATOGENOUS DIABETES ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PAPILLARY SEROUS ENDOMETRIAL CARCINOMA ( 1 FDA reports)
PARACENTESIS EYE ABNORMAL ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOLOGY TEST ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE DISCHARGE ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PEPTIC ULCER PERFORATION, OBSTRUCTIVE ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICA ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATYBASIA ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CONSTIPATION ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC EPILEPSY ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIATION DYSPHAGIA ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIATION PERICARDITIS ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RASH PSORIAFORM ( 1 FDA reports)
RECTAL CANCER STAGE II ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFSUM'S DISEASE ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY DISSECTION ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TUMOUR EXCISION ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHITIS ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL CYST ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOPHRENIA SIMPLE ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN GRAFT FAILURE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, MIXED TYPE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPECIFIC GRAVITY BODY FLUID ABNORMAL ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPIGELIAN HERNIA ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL FRACTURE ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TAENIASIS ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THORACOTOMY ( 1 FDA reports)
THOUGHT INSERTION ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYMUS ENLARGEMENT ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
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TINEA VERSICOLOUR ( 1 FDA reports)
TONGUE GEOGRAPHIC ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLITIS BACTERIAL ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC DILATATION OF COLON ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC ARTHROPATHY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
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TRISOMY 21 ( 1 FDA reports)
TROPONIN ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TYMPANIC MEMBRANE SCARRING ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD COMPRESSION ( 1 FDA reports)
UMBILICAL CORD SHORT ( 1 FDA reports)
UMBILICAL ERYTHEMA ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERAL POLYP ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL CARBUNCLE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URETHRITIS NONINFECTIVE ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE OUTPUT ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
URTICARIA AQUAGENIC ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VAGINITIS ( 1 FDA reports)
VANILLYL MANDELIC ACID URINE INCREASED ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VEIN WALL HYPERTROPHY ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOUS ANEURYSM ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIBRATORY SENSE INCREASED ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVECTOMY ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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