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

NAUSEA ( 3310 FDA reports)
ANXIETY ( 3247 FDA reports)
DEPRESSION ( 3199 FDA reports)
PAIN ( 2963 FDA reports)
FATIGUE ( 2551 FDA reports)
HEADACHE ( 2228 FDA reports)
DIZZINESS ( 2189 FDA reports)
DYSPNOEA ( 2115 FDA reports)
VOMITING ( 1985 FDA reports)
DIARRHOEA ( 1911 FDA reports)
FALL ( 1843 FDA reports)
INSOMNIA ( 1821 FDA reports)
DRUG INEFFECTIVE ( 1712 FDA reports)
ASTHENIA ( 1596 FDA reports)
SUICIDAL IDEATION ( 1565 FDA reports)
CHEST PAIN ( 1436 FDA reports)
BACK PAIN ( 1417 FDA reports)
WEIGHT DECREASED ( 1367 FDA reports)
WEIGHT INCREASED ( 1347 FDA reports)
ARTHRALGIA ( 1344 FDA reports)
PAIN IN EXTREMITY ( 1316 FDA reports)
CONVULSION ( 1276 FDA reports)
ABDOMINAL PAIN ( 1227 FDA reports)
DIABETES MELLITUS ( 1224 FDA reports)
ANAEMIA ( 1208 FDA reports)
OEDEMA PERIPHERAL ( 1202 FDA reports)
TREMOR ( 1185 FDA reports)
INJURY ( 1145 FDA reports)
HYPERTENSION ( 1130 FDA reports)
FEELING ABNORMAL ( 1098 FDA reports)
CONFUSIONAL STATE ( 1085 FDA reports)
RASH ( 1061 FDA reports)
CONSTIPATION ( 1052 FDA reports)
PYREXIA ( 1047 FDA reports)
SOMNOLENCE ( 997 FDA reports)
PNEUMONIA ( 987 FDA reports)
DEHYDRATION ( 973 FDA reports)
TYPE 2 DIABETES MELLITUS ( 963 FDA reports)
PARAESTHESIA ( 922 FDA reports)
PULMONARY EMBOLISM ( 915 FDA reports)
HYPERHIDROSIS ( 904 FDA reports)
LOSS OF CONSCIOUSNESS ( 899 FDA reports)
CONDITION AGGRAVATED ( 894 FDA reports)
HYPOAESTHESIA ( 854 FDA reports)
URINARY TRACT INFECTION ( 834 FDA reports)
MALAISE ( 825 FDA reports)
SUICIDE ATTEMPT ( 804 FDA reports)
AMNESIA ( 787 FDA reports)
EMOTIONAL DISTRESS ( 780 FDA reports)
DEEP VEIN THROMBOSIS ( 762 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 755 FDA reports)
MUSCLE SPASMS ( 755 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 750 FDA reports)
COUGH ( 738 FDA reports)
DECREASED APPETITE ( 738 FDA reports)
AGITATION ( 728 FDA reports)
HYPOTENSION ( 727 FDA reports)
ABDOMINAL PAIN UPPER ( 716 FDA reports)
CEREBROVASCULAR ACCIDENT ( 714 FDA reports)
GAIT DISTURBANCE ( 707 FDA reports)
NEUROPATHY PERIPHERAL ( 696 FDA reports)
VISION BLURRED ( 692 FDA reports)
PRURITUS ( 674 FDA reports)
DRUG INTERACTION ( 673 FDA reports)
PALPITATIONS ( 649 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 647 FDA reports)
OSTEONECROSIS OF JAW ( 641 FDA reports)
MYOCARDIAL INFARCTION ( 634 FDA reports)
SYNCOPE ( 633 FDA reports)
OSTEOARTHRITIS ( 629 FDA reports)
COMPLETED SUICIDE ( 619 FDA reports)
ANHEDONIA ( 614 FDA reports)
MEMORY IMPAIRMENT ( 613 FDA reports)
MYALGIA ( 613 FDA reports)
BLOOD GLUCOSE INCREASED ( 610 FDA reports)
OVERDOSE ( 602 FDA reports)
CHOLELITHIASIS ( 590 FDA reports)
BRONCHITIS ( 586 FDA reports)
MUSCULAR WEAKNESS ( 574 FDA reports)
DYSPHAGIA ( 571 FDA reports)
DEATH ( 558 FDA reports)
BONE DISORDER ( 557 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 556 FDA reports)
BLOOD PRESSURE INCREASED ( 548 FDA reports)
CONTUSION ( 542 FDA reports)
PANCREATITIS ( 538 FDA reports)
RENAL FAILURE ( 537 FDA reports)
ERYTHEMA ( 533 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 515 FDA reports)
DYSPEPSIA ( 515 FDA reports)
AGGRESSION ( 509 FDA reports)
SPINAL OSTEOARTHRITIS ( 509 FDA reports)
SINUSITIS ( 503 FDA reports)
HALLUCINATION ( 496 FDA reports)
PANIC ATTACK ( 485 FDA reports)
NECK PAIN ( 484 FDA reports)
PLEURAL EFFUSION ( 479 FDA reports)
ROAD TRAFFIC ACCIDENT ( 478 FDA reports)
ATRIAL FIBRILLATION ( 477 FDA reports)
CHEST DISCOMFORT ( 474 FDA reports)
IRRITABILITY ( 474 FDA reports)
ABNORMAL BEHAVIOUR ( 464 FDA reports)
LETHARGY ( 461 FDA reports)
NERVOUSNESS ( 457 FDA reports)
HYPERLIPIDAEMIA ( 453 FDA reports)
BALANCE DISORDER ( 452 FDA reports)
RENAL FAILURE ACUTE ( 450 FDA reports)
INFECTION ( 444 FDA reports)
DRY MOUTH ( 439 FDA reports)
MENTAL STATUS CHANGES ( 439 FDA reports)
CHILLS ( 429 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 424 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 420 FDA reports)
CELLULITIS ( 416 FDA reports)
HEART RATE INCREASED ( 416 FDA reports)
METASTASES TO BONE ( 416 FDA reports)
ANGER ( 413 FDA reports)
CHOLECYSTITIS CHRONIC ( 413 FDA reports)
HYPERSENSITIVITY ( 413 FDA reports)
STRESS ( 413 FDA reports)
DISTURBANCE IN ATTENTION ( 409 FDA reports)
HYPOKALAEMIA ( 409 FDA reports)
OBESITY ( 407 FDA reports)
ARTHRITIS ( 406 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 401 FDA reports)
SLEEP APNOEA SYNDROME ( 401 FDA reports)
MIGRAINE ( 394 FDA reports)
MENTAL DISORDER ( 385 FDA reports)
OSTEOMYELITIS ( 385 FDA reports)
DYSKINESIA ( 384 FDA reports)
SWELLING ( 383 FDA reports)
HAEMOGLOBIN DECREASED ( 382 FDA reports)
INFLUENZA LIKE ILLNESS ( 382 FDA reports)
ATELECTASIS ( 380 FDA reports)
BONE PAIN ( 376 FDA reports)
PAIN IN JAW ( 374 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 373 FDA reports)
OSTEONECROSIS ( 373 FDA reports)
URTICARIA ( 368 FDA reports)
TACHYCARDIA ( 367 FDA reports)
ABDOMINAL DISTENSION ( 363 FDA reports)
THROMBOCYTOPENIA ( 361 FDA reports)
ALOPECIA ( 352 FDA reports)
CARDIOMEGALY ( 348 FDA reports)
CRYING ( 347 FDA reports)
ABNORMAL DREAMS ( 343 FDA reports)
THROMBOSIS ( 342 FDA reports)
CARDIAC DISORDER ( 341 FDA reports)
FLUSHING ( 341 FDA reports)
MUSCULOSKELETAL PAIN ( 340 FDA reports)
GALLBLADDER DISORDER ( 336 FDA reports)
IMPAIRED HEALING ( 335 FDA reports)
HYPERGLYCAEMIA ( 328 FDA reports)
SLEEP DISORDER ( 328 FDA reports)
DRUG DOSE OMISSION ( 325 FDA reports)
BIPOLAR DISORDER ( 324 FDA reports)
PARANOIA ( 324 FDA reports)
DYSGEUSIA ( 323 FDA reports)
ASTHMA ( 322 FDA reports)
HOT FLUSH ( 320 FDA reports)
RESPIRATORY FAILURE ( 319 FDA reports)
DISORIENTATION ( 318 FDA reports)
HYPONATRAEMIA ( 317 FDA reports)
JOINT SWELLING ( 316 FDA reports)
SEPSIS ( 314 FDA reports)
RESTLESSNESS ( 313 FDA reports)
CORONARY ARTERY DISEASE ( 312 FDA reports)
NIGHTMARE ( 311 FDA reports)
TOOTH EXTRACTION ( 308 FDA reports)
TARDIVE DYSKINESIA ( 305 FDA reports)
SPEECH DISORDER ( 304 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 303 FDA reports)
PLATELET COUNT DECREASED ( 303 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 300 FDA reports)
OEDEMA ( 297 FDA reports)
HAEMORRHOIDS ( 294 FDA reports)
MANIA ( 294 FDA reports)
DENTAL CARIES ( 293 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 292 FDA reports)
TINNITUS ( 291 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 290 FDA reports)
PSYCHOTIC DISORDER ( 289 FDA reports)
NEPHROLITHIASIS ( 288 FDA reports)
INJECTION SITE PAIN ( 283 FDA reports)
NIGHT SWEATS ( 283 FDA reports)
FEAR ( 282 FDA reports)
TREATMENT NONCOMPLIANCE ( 282 FDA reports)
URINARY INCONTINENCE ( 282 FDA reports)
HEAD INJURY ( 280 FDA reports)
ABDOMINAL DISCOMFORT ( 279 FDA reports)
EPISTAXIS ( 278 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 277 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 277 FDA reports)
MITRAL VALVE INCOMPETENCE ( 273 FDA reports)
PANCYTOPENIA ( 273 FDA reports)
VERTIGO ( 270 FDA reports)
ANOREXIA ( 268 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 267 FDA reports)
OSTEOPENIA ( 267 FDA reports)
MOOD SWINGS ( 265 FDA reports)
DYSURIA ( 262 FDA reports)
DYSARTHRIA ( 261 FDA reports)
GASTRITIS ( 260 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 260 FDA reports)
FLATULENCE ( 259 FDA reports)
HEPATIC STEATOSIS ( 256 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 251 FDA reports)
ECONOMIC PROBLEM ( 248 FDA reports)
CARDIAC ARREST ( 246 FDA reports)
DRUG EFFECT DECREASED ( 246 FDA reports)
HIATUS HERNIA ( 246 FDA reports)
OSTEOPOROSIS ( 245 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 245 FDA reports)
UNEVALUABLE EVENT ( 243 FDA reports)
RECTAL HAEMORRHAGE ( 242 FDA reports)
HYPOTHYROIDISM ( 242 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 241 FDA reports)
DYSPNOEA EXERTIONAL ( 240 FDA reports)
INTENTIONAL OVERDOSE ( 240 FDA reports)
MUSCLE TWITCHING ( 239 FDA reports)
DEFORMITY ( 238 FDA reports)
THINKING ABNORMAL ( 238 FDA reports)
TOOTHACHE ( 236 FDA reports)
BLOOD PRESSURE DECREASED ( 235 FDA reports)
GRAND MAL CONVULSION ( 234 FDA reports)
HYPOGLYCAEMIA ( 234 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 233 FDA reports)
VISUAL IMPAIRMENT ( 233 FDA reports)
DIABETIC NEUROPATHY ( 232 FDA reports)
FEELING HOT ( 230 FDA reports)
POLLAKIURIA ( 229 FDA reports)
URINARY RETENTION ( 229 FDA reports)
SWELLING FACE ( 225 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 225 FDA reports)
ABASIA ( 225 FDA reports)
LUNG NEOPLASM ( 224 FDA reports)
DIPLOPIA ( 223 FDA reports)
DIABETIC KETOACIDOSIS ( 222 FDA reports)
OFF LABEL USE ( 222 FDA reports)
MAJOR DEPRESSION ( 221 FDA reports)
ARRHYTHMIA ( 220 FDA reports)
CATARACT ( 220 FDA reports)
DEPRESSED MOOD ( 217 FDA reports)
LYMPHADENOPATHY ( 217 FDA reports)
STAPHYLOCOCCAL INFECTION ( 217 FDA reports)
TOOTH DISORDER ( 216 FDA reports)
COMA ( 216 FDA reports)
BURNING SENSATION ( 215 FDA reports)
DIVERTICULUM ( 215 FDA reports)
RESTLESS LEGS SYNDROME ( 215 FDA reports)
APHASIA ( 213 FDA reports)
DRUG DEPENDENCE ( 213 FDA reports)
MEDICATION ERROR ( 210 FDA reports)
RENAL FAILURE CHRONIC ( 210 FDA reports)
INCORRECT DOSE ADMINISTERED ( 206 FDA reports)
PULMONARY OEDEMA ( 206 FDA reports)
WITHDRAWAL SYNDROME ( 205 FDA reports)
BLOOD CREATININE INCREASED ( 204 FDA reports)
DISABILITY ( 204 FDA reports)
DECREASED INTEREST ( 203 FDA reports)
EAR PAIN ( 202 FDA reports)
TOOTH LOSS ( 202 FDA reports)
HYPERSOMNIA ( 201 FDA reports)
PREGNANCY ( 201 FDA reports)
CANDIDIASIS ( 200 FDA reports)
HAEMORRHAGE ( 200 FDA reports)
NEUTROPENIA ( 200 FDA reports)
SCAR ( 200 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 200 FDA reports)
MOBILITY DECREASED ( 198 FDA reports)
CARDIAC MURMUR ( 197 FDA reports)
NASOPHARYNGITIS ( 197 FDA reports)
RENAL CYST ( 197 FDA reports)
OROPHARYNGEAL PAIN ( 196 FDA reports)
PRODUCT QUALITY ISSUE ( 196 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 194 FDA reports)
RIB FRACTURE ( 194 FDA reports)
ARTHROPATHY ( 193 FDA reports)
PERICARDIAL EFFUSION ( 193 FDA reports)
EMOTIONAL DISORDER ( 191 FDA reports)
HYPOXIA ( 191 FDA reports)
COGNITIVE DISORDER ( 189 FDA reports)
FEMUR FRACTURE ( 189 FDA reports)
HAEMATOCHEZIA ( 188 FDA reports)
BLOOD GLUCOSE DECREASED ( 187 FDA reports)
EXOSTOSIS ( 187 FDA reports)
FOOT FRACTURE ( 187 FDA reports)
PULMONARY HYPERTENSION ( 187 FDA reports)
FIBROMYALGIA ( 186 FDA reports)
HALLUCINATION, AUDITORY ( 186 FDA reports)
INJECTION SITE ERYTHEMA ( 186 FDA reports)
ERECTILE DYSFUNCTION ( 185 FDA reports)
HAEMATOCRIT DECREASED ( 185 FDA reports)
HERPES ZOSTER ( 185 FDA reports)
LUNG INFILTRATION ( 185 FDA reports)
DRY SKIN ( 183 FDA reports)
LEUKOPENIA ( 183 FDA reports)
TOOTH FRACTURE ( 183 FDA reports)
UNRESPONSIVE TO STIMULI ( 182 FDA reports)
DYSPHONIA ( 182 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 182 FDA reports)
NEURALGIA ( 182 FDA reports)
IRRITABLE BOWEL SYNDROME ( 181 FDA reports)
TYPE 1 DIABETES MELLITUS ( 181 FDA reports)
SEDATION ( 179 FDA reports)
DRUG HYPERSENSITIVITY ( 179 FDA reports)
NEOPLASM MALIGNANT ( 178 FDA reports)
ANGINA PECTORIS ( 177 FDA reports)
INTENTIONAL SELF-INJURY ( 177 FDA reports)
BLOOD POTASSIUM DECREASED ( 176 FDA reports)
MOUTH ULCERATION ( 176 FDA reports)
BRADYCARDIA ( 175 FDA reports)
DRUG TOXICITY ( 175 FDA reports)
WHEEZING ( 175 FDA reports)
GUN SHOT WOUND ( 173 FDA reports)
MULTIPLE SCLEROSIS ( 173 FDA reports)
GASTROINTESTINAL DISORDER ( 171 FDA reports)
CHOLECYSTITIS ( 169 FDA reports)
SKIN LESION ( 169 FDA reports)
HEPATIC ENZYME INCREASED ( 168 FDA reports)
HIP FRACTURE ( 168 FDA reports)
IMPAIRED DRIVING ABILITY ( 168 FDA reports)
LUNG DISORDER ( 168 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 168 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 168 FDA reports)
ORAL PAIN ( 168 FDA reports)
EYE PAIN ( 167 FDA reports)
SURGERY ( 166 FDA reports)
SEROTONIN SYNDROME ( 165 FDA reports)
CARDIO-RESPIRATORY ARREST ( 165 FDA reports)
EATING DISORDER ( 165 FDA reports)
BONE LESION ( 164 FDA reports)
SCOLIOSIS ( 163 FDA reports)
RESPIRATORY DISTRESS ( 162 FDA reports)
ILL-DEFINED DISORDER ( 162 FDA reports)
TOOTH ABSCESS ( 161 FDA reports)
METASTASES TO LIVER ( 160 FDA reports)
NASAL CONGESTION ( 160 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 159 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 159 FDA reports)
COLITIS ( 158 FDA reports)
STOMATITIS ( 158 FDA reports)
CROHN'S DISEASE ( 157 FDA reports)
NERVOUS SYSTEM DISORDER ( 157 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 155 FDA reports)
HYPOPHAGIA ( 155 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 155 FDA reports)
DISEASE PROGRESSION ( 154 FDA reports)
INFLAMMATION ( 154 FDA reports)
INTENTIONAL DRUG MISUSE ( 154 FDA reports)
FAECAL INCONTINENCE ( 153 FDA reports)
HAEMATURIA ( 152 FDA reports)
LIBIDO DECREASED ( 152 FDA reports)
MULTIPLE MYELOMA ( 152 FDA reports)
FUNGAL INFECTION ( 151 FDA reports)
RHINORRHOEA ( 151 FDA reports)
SPINAL COLUMN STENOSIS ( 150 FDA reports)
MULTIPLE INJURIES ( 150 FDA reports)
BREAST CANCER ( 149 FDA reports)
IMPAIRED WORK ABILITY ( 149 FDA reports)
BLOOD UREA INCREASED ( 147 FDA reports)
PANCREATITIS ACUTE ( 147 FDA reports)
SINUS TACHYCARDIA ( 147 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 146 FDA reports)
INFLUENZA ( 146 FDA reports)
CHOLECYSTECTOMY ( 144 FDA reports)
DELIRIUM ( 144 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 144 FDA reports)
MENTAL IMPAIRMENT ( 144 FDA reports)
RETCHING ( 144 FDA reports)
THYROID DISORDER ( 144 FDA reports)
GINGIVAL PAIN ( 142 FDA reports)
DRY EYE ( 141 FDA reports)
EMPHYSEMA ( 141 FDA reports)
BURSITIS ( 140 FDA reports)
CARPAL TUNNEL SYNDROME ( 140 FDA reports)
HEART RATE IRREGULAR ( 138 FDA reports)
DEAFNESS ( 137 FDA reports)
OXYGEN SATURATION DECREASED ( 137 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 137 FDA reports)
SKIN DISORDER ( 137 FDA reports)
CARDIOMYOPATHY ( 136 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 136 FDA reports)
FLUID RETENTION ( 135 FDA reports)
PULMONARY CONGESTION ( 135 FDA reports)
VISUAL ACUITY REDUCED ( 135 FDA reports)
RENAL DISORDER ( 134 FDA reports)
SWOLLEN TONGUE ( 134 FDA reports)
ACCIDENTAL OVERDOSE ( 132 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 132 FDA reports)
HYPERCHOLESTEROLAEMIA ( 131 FDA reports)
MENISCUS LESION ( 131 FDA reports)
AKATHISIA ( 130 FDA reports)
ARTERIOSCLEROSIS ( 130 FDA reports)
DISCOMFORT ( 130 FDA reports)
RHEUMATOID ARTHRITIS ( 130 FDA reports)
RENAL IMPAIRMENT ( 129 FDA reports)
BLOOD SODIUM DECREASED ( 129 FDA reports)
PALLOR ( 129 FDA reports)
COMPRESSION FRACTURE ( 128 FDA reports)
CYSTITIS ( 128 FDA reports)
FEBRILE NEUTROPENIA ( 126 FDA reports)
GASTRIC DISORDER ( 126 FDA reports)
GROIN PAIN ( 126 FDA reports)
HAEMOPTYSIS ( 126 FDA reports)
LUMBAR SPINAL STENOSIS ( 126 FDA reports)
MALNUTRITION ( 126 FDA reports)
MOOD ALTERED ( 126 FDA reports)
PHARYNGEAL OEDEMA ( 125 FDA reports)
BLINDNESS ( 124 FDA reports)
COORDINATION ABNORMAL ( 124 FDA reports)
DELUSION ( 124 FDA reports)
PERSONALITY CHANGE ( 124 FDA reports)
VIRAL INFECTION ( 124 FDA reports)
TENDONITIS ( 123 FDA reports)
FEELING JITTERY ( 123 FDA reports)
JOINT INJURY ( 123 FDA reports)
LACERATION ( 123 FDA reports)
PATHOLOGICAL FRACTURE ( 122 FDA reports)
APATHY ( 120 FDA reports)
HEART RATE DECREASED ( 120 FDA reports)
JAW DISORDER ( 120 FDA reports)
ROTATOR CUFF SYNDROME ( 120 FDA reports)
SKIN DISCOLOURATION ( 120 FDA reports)
SOMNAMBULISM ( 120 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 120 FDA reports)
RASH PRURITIC ( 119 FDA reports)
DYSTONIA ( 119 FDA reports)
ORTHOSTATIC HYPOTENSION ( 119 FDA reports)
GLAUCOMA ( 118 FDA reports)
PSORIASIS ( 118 FDA reports)
SINUS BRADYCARDIA ( 118 FDA reports)
EYE DISORDER ( 117 FDA reports)
GASTROENTERITIS ( 117 FDA reports)
ABSCESS ( 116 FDA reports)
CHRONIC SINUSITIS ( 116 FDA reports)
HALLUCINATION, VISUAL ( 116 FDA reports)
HEMIPARESIS ( 116 FDA reports)
JOINT EFFUSION ( 116 FDA reports)
MASTICATION DISORDER ( 116 FDA reports)
PNEUMONIA ASPIRATION ( 115 FDA reports)
RHABDOMYOLYSIS ( 115 FDA reports)
ENCEPHALOPATHY ( 114 FDA reports)
FLUID OVERLOAD ( 113 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 113 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 113 FDA reports)
SELF-INJURIOUS IDEATION ( 113 FDA reports)
BLISTER ( 112 FDA reports)
DECUBITUS ULCER ( 112 FDA reports)
ENDODONTIC PROCEDURE ( 112 FDA reports)
HEPATOMEGALY ( 112 FDA reports)
JAW OPERATION ( 112 FDA reports)
INJECTION SITE HAEMORRHAGE ( 111 FDA reports)
JAUNDICE ( 111 FDA reports)
RASH GENERALISED ( 111 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 110 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 110 FDA reports)
BILIARY DYSKINESIA ( 110 FDA reports)
BRUXISM ( 110 FDA reports)
HAEMATEMESIS ( 110 FDA reports)
OSTEOLYSIS ( 110 FDA reports)
HEPATIC CYST ( 109 FDA reports)
CYST ( 108 FDA reports)
INCONTINENCE ( 108 FDA reports)
TEARFULNESS ( 108 FDA reports)
VAGINAL HAEMORRHAGE ( 108 FDA reports)
SKIN EXFOLIATION ( 107 FDA reports)
ADVERSE DRUG REACTION ( 107 FDA reports)
DIABETIC COMA ( 107 FDA reports)
MULTI-ORGAN FAILURE ( 107 FDA reports)
BLOOD CALCIUM DECREASED ( 106 FDA reports)
METASTASES TO LUNG ( 106 FDA reports)
MOVEMENT DISORDER ( 106 FDA reports)
PRESYNCOPE ( 106 FDA reports)
INCREASED APPETITE ( 105 FDA reports)
MASS ( 105 FDA reports)
VENTRICULAR TACHYCARDIA ( 105 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 104 FDA reports)
SKIN ULCER ( 104 FDA reports)
AFFECTIVE DISORDER ( 104 FDA reports)
DRUG ABUSE ( 104 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 104 FDA reports)
HOMICIDAL IDEATION ( 104 FDA reports)
INJECTION SITE HAEMATOMA ( 104 FDA reports)
OESOPHAGITIS ( 104 FDA reports)
ORAL DISORDER ( 104 FDA reports)
ALCOHOL USE ( 103 FDA reports)
CAESAREAN SECTION ( 103 FDA reports)
CEREBRAL ATROPHY ( 103 FDA reports)
DYSSTASIA ( 103 FDA reports)
GINGIVAL DISORDER ( 103 FDA reports)
BLOOD BILIRUBIN INCREASED ( 102 FDA reports)
COLD SWEAT ( 102 FDA reports)
HYPOVOLAEMIA ( 102 FDA reports)
POST PROCEDURAL COMPLICATION ( 102 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 102 FDA reports)
ORAL INFECTION ( 101 FDA reports)
PRURITUS GENERALISED ( 101 FDA reports)
ADVERSE EVENT ( 100 FDA reports)
ASCITES ( 100 FDA reports)
DEMENTIA ( 100 FDA reports)
FLANK PAIN ( 100 FDA reports)
RESPIRATORY ARREST ( 100 FDA reports)
HYPERKALAEMIA ( 99 FDA reports)
HYPOAESTHESIA ORAL ( 99 FDA reports)
MENORRHAGIA ( 99 FDA reports)
MIDDLE INSOMNIA ( 99 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 98 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 98 FDA reports)
DIVERTICULITIS ( 98 FDA reports)
EYE SWELLING ( 98 FDA reports)
HEPATITIS ( 98 FDA reports)
PELVIC PAIN ( 98 FDA reports)
PLEURITIC PAIN ( 98 FDA reports)
PURULENT DISCHARGE ( 98 FDA reports)
SKIN LACERATION ( 98 FDA reports)
VISUAL DISTURBANCE ( 97 FDA reports)
ANKLE FRACTURE ( 97 FDA reports)
BACTERIAL INFECTION ( 97 FDA reports)
DEBRIDEMENT ( 97 FDA reports)
DISEASE RECURRENCE ( 97 FDA reports)
GASTRIC ULCER ( 97 FDA reports)
HAEMATOMA ( 97 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 97 FDA reports)
ABORTION SPONTANEOUS ( 96 FDA reports)
MYOCARDIAL ISCHAEMIA ( 96 FDA reports)
PATHOLOGICAL GAMBLING ( 96 FDA reports)
FISTULA ( 95 FDA reports)
LEUKOCYTOSIS ( 95 FDA reports)
OVARIAN CYST ( 95 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 95 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 95 FDA reports)
TOOTH INFECTION ( 95 FDA reports)
EJECTION FRACTION DECREASED ( 94 FDA reports)
HEPATITIS C ( 94 FDA reports)
MULTIPLE DRUG OVERDOSE ( 94 FDA reports)
ATAXIA ( 93 FDA reports)
BREAST MASS ( 93 FDA reports)
JOINT STIFFNESS ( 93 FDA reports)
DIVERTICULUM INTESTINAL ( 92 FDA reports)
MUSCLE TIGHTNESS ( 92 FDA reports)
OSTEITIS ( 92 FDA reports)
SEXUAL DYSFUNCTION ( 92 FDA reports)
UPPER LIMB FRACTURE ( 91 FDA reports)
UTERINE LEIOMYOMA ( 91 FDA reports)
AORTIC ANEURYSM ( 91 FDA reports)
BODY TEMPERATURE INCREASED ( 91 FDA reports)
CHOLECYSTITIS ACUTE ( 91 FDA reports)
DRUG SCREEN POSITIVE ( 90 FDA reports)
HEPATIC FAILURE ( 90 FDA reports)
LIMB INJURY ( 90 FDA reports)
MITRAL VALVE PROLAPSE ( 90 FDA reports)
ORAL CANDIDIASIS ( 90 FDA reports)
CARDIAC FAILURE ( 89 FDA reports)
COLONIC POLYP ( 89 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 89 FDA reports)
GOITRE ( 89 FDA reports)
LIVER DISORDER ( 89 FDA reports)
LUNG NEOPLASM MALIGNANT ( 89 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 89 FDA reports)
SEPTIC SHOCK ( 89 FDA reports)
TENDERNESS ( 89 FDA reports)
STEVENS-JOHNSON SYNDROME ( 88 FDA reports)
BREAST PAIN ( 88 FDA reports)
FEELING COLD ( 88 FDA reports)
PNEUMOTHORAX ( 88 FDA reports)
DRUG INTOLERANCE ( 87 FDA reports)
EXPOSED BONE IN JAW ( 87 FDA reports)
JAW FRACTURE ( 87 FDA reports)
PHARYNGITIS ( 86 FDA reports)
PROCEDURAL PAIN ( 86 FDA reports)
HOSTILITY ( 85 FDA reports)
HYPERCALCAEMIA ( 85 FDA reports)
RESPIRATORY DISORDER ( 85 FDA reports)
RHINITIS ALLERGIC ( 85 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 85 FDA reports)
RASH ERYTHEMATOUS ( 84 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 84 FDA reports)
ATRIAL SEPTAL DEFECT ( 84 FDA reports)
BONE DENSITY DECREASED ( 84 FDA reports)
FAECES DISCOLOURED ( 84 FDA reports)
LUMBAR RADICULOPATHY ( 84 FDA reports)
MUSCLE STRAIN ( 84 FDA reports)
ORAL INTAKE REDUCED ( 84 FDA reports)
PREMATURE BABY ( 84 FDA reports)
ANAPHYLACTIC REACTION ( 83 FDA reports)
DYSLIPIDAEMIA ( 83 FDA reports)
LACRIMATION INCREASED ( 83 FDA reports)
PANIC REACTION ( 83 FDA reports)
PRODUCTIVE COUGH ( 83 FDA reports)
SENSORY DISTURBANCE ( 83 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 83 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 83 FDA reports)
SENSATION OF HEAVINESS ( 82 FDA reports)
SPONDYLOLISTHESIS ( 82 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 82 FDA reports)
COAGULOPATHY ( 82 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 82 FDA reports)
INTENTIONAL MISUSE ( 82 FDA reports)
CORONARY ARTERY OCCLUSION ( 81 FDA reports)
CYANOSIS ( 81 FDA reports)
EXCORIATION ( 81 FDA reports)
HYPERKERATOSIS ( 81 FDA reports)
POOR QUALITY SLEEP ( 81 FDA reports)
PROTEINURIA ( 81 FDA reports)
PULMONARY FIBROSIS ( 81 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 81 FDA reports)
RENAL INJURY ( 80 FDA reports)
SPLENOMEGALY ( 80 FDA reports)
AGEUSIA ( 80 FDA reports)
MUCOSAL INFLAMMATION ( 80 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 80 FDA reports)
BASAL CELL CARCINOMA ( 79 FDA reports)
BLOOD POTASSIUM INCREASED ( 79 FDA reports)
DRUG ADMINISTRATION ERROR ( 79 FDA reports)
ODYNOPHAGIA ( 79 FDA reports)
RHINITIS ( 79 FDA reports)
SKIN INDURATION ( 79 FDA reports)
THROAT TIGHTNESS ( 79 FDA reports)
SPINAL FRACTURE ( 78 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 78 FDA reports)
BACK INJURY ( 78 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 78 FDA reports)
DEVICE RELATED INFECTION ( 78 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 78 FDA reports)
FACET JOINT SYNDROME ( 78 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 78 FDA reports)
MELAENA ( 78 FDA reports)
METRORRHAGIA ( 78 FDA reports)
PRIMARY SEQUESTRUM ( 78 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 77 FDA reports)
GINGIVAL SWELLING ( 77 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 77 FDA reports)
MICTURITION URGENCY ( 77 FDA reports)
NEOPLASM PROGRESSION ( 77 FDA reports)
OSTEOSCLEROSIS ( 77 FDA reports)
THROAT IRRITATION ( 77 FDA reports)
RASH MACULAR ( 76 FDA reports)
AFFECT LABILITY ( 76 FDA reports)
ELECTROLYTE IMBALANCE ( 76 FDA reports)
FACIAL PAIN ( 76 FDA reports)
FIBROSIS ( 76 FDA reports)
ILEUS ( 76 FDA reports)
INCOHERENT ( 76 FDA reports)
INFUSION RELATED REACTION ( 76 FDA reports)
INTERSTITIAL LUNG DISEASE ( 76 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 76 FDA reports)
POLYURIA ( 76 FDA reports)
AZOTAEMIA ( 75 FDA reports)
BLOOD URINE PRESENT ( 75 FDA reports)
DIABETIC RETINOPATHY ( 75 FDA reports)
ECZEMA ( 75 FDA reports)
GLOSSODYNIA ( 75 FDA reports)
SCREAMING ( 75 FDA reports)
SYNOVIAL CYST ( 75 FDA reports)
VITAMIN D DEFICIENCY ( 74 FDA reports)
BACK DISORDER ( 74 FDA reports)
CEREBRAL HAEMORRHAGE ( 74 FDA reports)
HAND FRACTURE ( 74 FDA reports)
ABDOMINAL PAIN LOWER ( 73 FDA reports)
DIALYSIS ( 73 FDA reports)
GINGIVITIS ( 73 FDA reports)
PLATELET COUNT INCREASED ( 73 FDA reports)
APNOEA ( 72 FDA reports)
MUSCLE INJURY ( 72 FDA reports)
SKIN TIGHTNESS ( 72 FDA reports)
SINUS CONGESTION ( 71 FDA reports)
ACUTE SINUSITIS ( 71 FDA reports)
BLADDER DISORDER ( 71 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 71 FDA reports)
EAR INFECTION ( 71 FDA reports)
FAILURE TO THRIVE ( 71 FDA reports)
FRACTURED SACRUM ( 71 FDA reports)
ACUTE RESPIRATORY FAILURE ( 70 FDA reports)
DIFFICULTY IN WALKING ( 70 FDA reports)
INJECTION SITE REACTION ( 70 FDA reports)
SEBORRHOEIC KERATOSIS ( 70 FDA reports)
ULCER ( 70 FDA reports)
ACNE ( 69 FDA reports)
DILATATION VENTRICULAR ( 69 FDA reports)
EUPHORIC MOOD ( 69 FDA reports)
FOOT DEFORMITY ( 69 FDA reports)
HEPATIC CIRRHOSIS ( 69 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 69 FDA reports)
ORAL CAVITY FISTULA ( 69 FDA reports)
PHOTOPHOBIA ( 69 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 68 FDA reports)
AMENORRHOEA ( 68 FDA reports)
ANGINA UNSTABLE ( 68 FDA reports)
CHOKING ( 68 FDA reports)
DEVICE FAILURE ( 68 FDA reports)
BACTERAEMIA ( 67 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 67 FDA reports)
DRUG ABUSER ( 67 FDA reports)
EYE IRRITATION ( 67 FDA reports)
IRON DEFICIENCY ANAEMIA ( 67 FDA reports)
ALCOHOLISM ( 66 FDA reports)
AORTIC VALVE INCOMPETENCE ( 66 FDA reports)
CONVERSION DISORDER ( 66 FDA reports)
INITIAL INSOMNIA ( 66 FDA reports)
INJECTION SITE PRURITUS ( 66 FDA reports)
KYPHOSIS ( 66 FDA reports)
LOBAR PNEUMONIA ( 66 FDA reports)
LYMPHOEDEMA ( 66 FDA reports)
METASTASES TO SPINE ( 66 FDA reports)
STOMACH DISCOMFORT ( 66 FDA reports)
SKIN BURNING SENSATION ( 65 FDA reports)
SKIN HYPERTROPHY ( 65 FDA reports)
ASPIRATION ( 65 FDA reports)
BILIARY COLIC ( 65 FDA reports)
BLINDNESS UNILATERAL ( 65 FDA reports)
CEREBRAL INFARCTION ( 65 FDA reports)
DERMATITIS ( 65 FDA reports)
PEPTIC ULCER ( 65 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 65 FDA reports)
BREAST CANCER METASTATIC ( 64 FDA reports)
DEVICE MALFUNCTION ( 64 FDA reports)
DIABETIC COMPLICATION ( 64 FDA reports)
ECCHYMOSIS ( 64 FDA reports)
LOOSE TOOTH ( 64 FDA reports)
LUNG INFECTION ( 64 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 64 FDA reports)
METABOLIC ACIDOSIS ( 64 FDA reports)
RENAL PAIN ( 64 FDA reports)
VITAMIN D DECREASED ( 64 FDA reports)
SINUS HEADACHE ( 63 FDA reports)
VENTRICULAR FIBRILLATION ( 63 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 63 FDA reports)
BONE DEBRIDEMENT ( 63 FDA reports)
FAMILY STRESS ( 63 FDA reports)
KIDNEY INFECTION ( 63 FDA reports)
CARDIAC VALVE DISEASE ( 62 FDA reports)
IMPULSIVE BEHAVIOUR ( 62 FDA reports)
INJURY ASPHYXIATION ( 62 FDA reports)
LOW TURNOVER OSTEOPATHY ( 62 FDA reports)
MYDRIASIS ( 62 FDA reports)
NON-CARDIAC CHEST PAIN ( 62 FDA reports)
OPEN WOUND ( 62 FDA reports)
PLANTAR FASCIITIS ( 62 FDA reports)
FACIAL BONES FRACTURE ( 61 FDA reports)
GENERALISED OEDEMA ( 61 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 61 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 61 FDA reports)
MUSCLE RIGIDITY ( 61 FDA reports)
NERVE INJURY ( 61 FDA reports)
PERIODONTAL DISEASE ( 61 FDA reports)
PERIODONTITIS ( 61 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 61 FDA reports)
SPINAL DISORDER ( 61 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 61 FDA reports)
WRIST FRACTURE ( 61 FDA reports)
SINUS DISORDER ( 60 FDA reports)
VITAMIN B12 DEFICIENCY ( 60 FDA reports)
BRONCHOSPASM ( 60 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 60 FDA reports)
CEREBRAL ISCHAEMIA ( 60 FDA reports)
HERPES SIMPLEX ( 60 FDA reports)
INTESTINAL OBSTRUCTION ( 60 FDA reports)
JOINT SPRAIN ( 60 FDA reports)
NOCTURIA ( 60 FDA reports)
PANIC DISORDER ( 60 FDA reports)
PARKINSON'S DISEASE ( 60 FDA reports)
PETECHIAE ( 60 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 59 FDA reports)
BIPOLAR I DISORDER ( 59 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 59 FDA reports)
INJECTION SITE SWELLING ( 59 FDA reports)
ONYCHOMYCOSIS ( 59 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 59 FDA reports)
THERAPY NON-RESPONDER ( 59 FDA reports)
RESPIRATORY TRACT INFECTION ( 58 FDA reports)
SUICIDAL BEHAVIOUR ( 58 FDA reports)
THIRST ( 58 FDA reports)
CERVICOBRACHIAL SYNDROME ( 58 FDA reports)
FACIAL PALSY ( 58 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 58 FDA reports)
HYPOCALCAEMIA ( 58 FDA reports)
OSTEORADIONECROSIS ( 58 FDA reports)
BONE LOSS ( 57 FDA reports)
BREAST TENDERNESS ( 57 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 57 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 57 FDA reports)
HYPERAESTHESIA ( 57 FDA reports)
HYPOMAGNESAEMIA ( 57 FDA reports)
INCREASED TENDENCY TO BRUISE ( 57 FDA reports)
LIMB DISCOMFORT ( 57 FDA reports)
NO ADVERSE EVENT ( 57 FDA reports)
PARALYSIS ( 57 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 57 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 57 FDA reports)
TENDON RUPTURE ( 57 FDA reports)
SELF-MEDICATION ( 56 FDA reports)
VITREOUS FLOATERS ( 56 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 56 FDA reports)
BONE FRAGMENTATION ( 56 FDA reports)
BRAIN OEDEMA ( 56 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 56 FDA reports)
CAROTID ARTERY STENOSIS ( 56 FDA reports)
FRUSTRATION ( 56 FDA reports)
NEUTROPHIL COUNT DECREASED ( 56 FDA reports)
PNEUMONITIS ( 56 FDA reports)
ABSCESS DRAINAGE ( 55 FDA reports)
ANGIOEDEMA ( 55 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 55 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 55 FDA reports)
FIBULA FRACTURE ( 55 FDA reports)
GALLBLADDER INJURY ( 55 FDA reports)
KNEE ARTHROPLASTY ( 55 FDA reports)
LIP SWELLING ( 55 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 55 FDA reports)
PROTHROMBIN TIME PROLONGED ( 55 FDA reports)
RALES ( 55 FDA reports)
RESPIRATORY TRACT CONGESTION ( 55 FDA reports)
SPINAL COMPRESSION FRACTURE ( 55 FDA reports)
VENTRICULAR HYPERTROPHY ( 55 FDA reports)
SCIATICA ( 54 FDA reports)
SPINAL LAMINECTOMY ( 54 FDA reports)
UMBILICAL HERNIA ( 54 FDA reports)
BLOOD IRON DECREASED ( 54 FDA reports)
EYE HAEMORRHAGE ( 54 FDA reports)
GASTROENTERITIS VIRAL ( 54 FDA reports)
HAEMANGIOMA ( 54 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 54 FDA reports)
LOSS OF EMPLOYMENT ( 54 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 54 FDA reports)
MYOCLONUS ( 54 FDA reports)
NECK INJURY ( 54 FDA reports)
NO THERAPEUTIC RESPONSE ( 54 FDA reports)
PERICARDITIS ( 54 FDA reports)
BLOOD ALBUMIN DECREASED ( 53 FDA reports)
DIASTOLIC DYSFUNCTION ( 53 FDA reports)
DRUG DISPENSING ERROR ( 53 FDA reports)
ERUCTATION ( 53 FDA reports)
FEELING OF DESPAIR ( 53 FDA reports)
HYPOMANIA ( 53 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 53 FDA reports)
LOCALISED INFECTION ( 53 FDA reports)
METASTASES TO LYMPH NODES ( 53 FDA reports)
OCULAR HYPERAEMIA ( 53 FDA reports)
ATRIAL FLUTTER ( 52 FDA reports)
CERVICAL SPINAL STENOSIS ( 52 FDA reports)
EPILEPSY ( 52 FDA reports)
FURUNCLE ( 52 FDA reports)
MENOPAUSE ( 52 FDA reports)
OEDEMA MOUTH ( 52 FDA reports)
STRESS FRACTURE ( 52 FDA reports)
THYROID NEOPLASM ( 52 FDA reports)
TIBIA FRACTURE ( 52 FDA reports)
RESPIRATORY RATE INCREASED ( 51 FDA reports)
SEROMA ( 51 FDA reports)
SLEEP WALKING ( 51 FDA reports)
TRISMUS ( 51 FDA reports)
ASPHYXIA ( 51 FDA reports)
BONE OPERATION ( 51 FDA reports)
BREAST CANCER RECURRENT ( 51 FDA reports)
CONCUSSION ( 51 FDA reports)
CONGENITAL ANOMALY ( 51 FDA reports)
GINGIVAL BLEEDING ( 51 FDA reports)
GINGIVAL INFECTION ( 51 FDA reports)
NEURITIS ( 51 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 51 FDA reports)
OBSESSIVE THOUGHTS ( 51 FDA reports)
PANCREATITIS CHRONIC ( 51 FDA reports)
PHYSICAL ASSAULT ( 51 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 50 FDA reports)
COMPLEX PARTIAL SEIZURES ( 50 FDA reports)
EDENTULOUS ( 50 FDA reports)
EXPIRED DRUG ADMINISTERED ( 50 FDA reports)
GENERALISED ANXIETY DISORDER ( 50 FDA reports)
GINGIVAL ULCERATION ( 50 FDA reports)
GLOSSITIS ( 50 FDA reports)
LYMPHOMA ( 50 FDA reports)
VENOUS INSUFFICIENCY ( 50 FDA reports)
TIC ( 49 FDA reports)
WOUND ( 49 FDA reports)
ANEURYSM ( 49 FDA reports)
CHONDROMALACIA ( 49 FDA reports)
EYE PRURITUS ( 49 FDA reports)
GOUT ( 49 FDA reports)
HYPOACUSIS ( 49 FDA reports)
JOINT DISLOCATION ( 49 FDA reports)
LABORATORY TEST ABNORMAL ( 49 FDA reports)
LARYNGITIS ( 49 FDA reports)
BREATH ODOUR ( 48 FDA reports)
COLITIS ULCERATIVE ( 48 FDA reports)
DENTURE WEARER ( 48 FDA reports)
DERMAL CYST ( 48 FDA reports)
GENITAL HERPES ( 48 FDA reports)
LOSS OF LIBIDO ( 48 FDA reports)
MYELODYSPLASTIC SYNDROME ( 48 FDA reports)
SUDDEN DEATH ( 48 FDA reports)
UTERINE HAEMORRHAGE ( 48 FDA reports)
VAGINAL INFECTION ( 48 FDA reports)
WOUND DRAINAGE ( 48 FDA reports)
SNEEZING ( 47 FDA reports)
SPINAL CORD COMPRESSION ( 47 FDA reports)
TONGUE DISORDER ( 47 FDA reports)
VARICOSE VEIN ( 47 FDA reports)
APPLICATION SITE ERYTHEMA ( 47 FDA reports)
BODY HEIGHT DECREASED ( 47 FDA reports)
BREAST CANCER FEMALE ( 47 FDA reports)
CLOSTRIDIAL INFECTION ( 47 FDA reports)
DENTAL CARE ( 47 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 47 FDA reports)
GESTATIONAL DIABETES ( 47 FDA reports)
HERNIA ( 47 FDA reports)
HYDRONEPHROSIS ( 47 FDA reports)
HYSTERECTOMY ( 47 FDA reports)
LOCAL SWELLING ( 47 FDA reports)
NODULE ( 47 FDA reports)
PHYSICAL DISABILITY ( 47 FDA reports)
ACUTE CORONARY SYNDROME ( 46 FDA reports)
APPLICATION SITE PRURITUS ( 46 FDA reports)
BLOOD CALCIUM INCREASED ( 46 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 46 FDA reports)
CERVICAL DYSPLASIA ( 46 FDA reports)
DROOLING ( 46 FDA reports)
DRUG PRESCRIBING ERROR ( 46 FDA reports)
EPICONDYLITIS ( 46 FDA reports)
HYPERVENTILATION ( 46 FDA reports)
JAUNDICE NEONATAL ( 46 FDA reports)
MUSCLE ATROPHY ( 46 FDA reports)
PERIPHERAL COLDNESS ( 46 FDA reports)
PULMONARY INFARCTION ( 46 FDA reports)
RASH PAPULAR ( 46 FDA reports)
RETINAL HAEMORRHAGE ( 46 FDA reports)
SENSORY LOSS ( 46 FDA reports)
URINE OUTPUT DECREASED ( 46 FDA reports)
VULVOVAGINAL DRYNESS ( 46 FDA reports)
RECTAL POLYP ( 45 FDA reports)
SENSITIVITY OF TEETH ( 45 FDA reports)
SKELETAL INJURY ( 45 FDA reports)
SOCIAL PROBLEM ( 45 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 45 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 45 FDA reports)
AORTIC STENOSIS ( 45 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 45 FDA reports)
CACHEXIA ( 45 FDA reports)
FLAT AFFECT ( 45 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 45 FDA reports)
INGROWING NAIL ( 45 FDA reports)
LOWER LIMB FRACTURE ( 45 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 45 FDA reports)
NEONATAL DISORDER ( 45 FDA reports)
PLASMACYTOSIS ( 45 FDA reports)
QUALITY OF LIFE DECREASED ( 45 FDA reports)
ABDOMINAL HERNIA ( 44 FDA reports)
APHTHOUS STOMATITIS ( 44 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 44 FDA reports)
CATARACT OPERATION ( 44 FDA reports)
CEREBROVASCULAR DISORDER ( 44 FDA reports)
HOSPITALISATION ( 44 FDA reports)
LEFT ATRIAL DILATATION ( 44 FDA reports)
MUSCLE SPASTICITY ( 44 FDA reports)
PNEUMONIA BACTERIAL ( 44 FDA reports)
PRESCRIBED OVERDOSE ( 44 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 44 FDA reports)
RASH MACULO-PAPULAR ( 44 FDA reports)
SEQUESTRECTOMY ( 44 FDA reports)
TENDON INJURY ( 44 FDA reports)
TOBACCO ABUSE ( 44 FDA reports)
TONGUE ULCERATION ( 44 FDA reports)
VASCULITIS ( 44 FDA reports)
SKIN CANCER ( 43 FDA reports)
SKIN INFECTION ( 43 FDA reports)
SUBCUTANEOUS ABSCESS ( 43 FDA reports)
ANOSMIA ( 43 FDA reports)
DENTAL FISTULA ( 43 FDA reports)
FOOD CRAVING ( 43 FDA reports)
HAEMOLYTIC ANAEMIA ( 43 FDA reports)
HUMERUS FRACTURE ( 43 FDA reports)
HYPOKINESIA ( 43 FDA reports)
MENSTRUATION IRREGULAR ( 43 FDA reports)
METABOLIC SYNDROME ( 43 FDA reports)
NEUROPATHY ( 43 FDA reports)
PETIT MAL EPILEPSY ( 43 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 42 FDA reports)
AORTIC CALCIFICATION ( 42 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 42 FDA reports)
DIABETIC NEPHROPATHY ( 42 FDA reports)
DYSPHEMIA ( 42 FDA reports)
ENERGY INCREASED ( 42 FDA reports)
FEMORAL NECK FRACTURE ( 42 FDA reports)
ORAL SURGERY ( 42 FDA reports)
OTITIS MEDIA ( 42 FDA reports)
SOFT TISSUE DISORDER ( 42 FDA reports)
STRESS URINARY INCONTINENCE ( 42 FDA reports)
WOUND DEHISCENCE ( 42 FDA reports)
SQUAMOUS CELL CARCINOMA ( 41 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 41 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 41 FDA reports)
ADJUSTMENT DISORDER ( 41 FDA reports)
BEDRIDDEN ( 41 FDA reports)
BLOOD MAGNESIUM DECREASED ( 41 FDA reports)
BONE NEOPLASM MALIGNANT ( 41 FDA reports)
CARDIOVASCULAR DISORDER ( 41 FDA reports)
COSTOCHONDRITIS ( 41 FDA reports)
DEPENDENCE ( 41 FDA reports)
DERMATITIS CONTACT ( 41 FDA reports)
DRUG LEVEL INCREASED ( 41 FDA reports)
EAR CONGESTION ( 41 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 41 FDA reports)
EYE INFECTION ( 41 FDA reports)
FACE INJURY ( 41 FDA reports)
HYPERPHAGIA ( 41 FDA reports)
HYPOAESTHESIA FACIAL ( 41 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 41 FDA reports)
LACUNAR INFARCTION ( 41 FDA reports)
MACULAR DEGENERATION ( 41 FDA reports)
NAIL DISORDER ( 41 FDA reports)
NEPHRITIS INTERSTITIAL ( 41 FDA reports)
PLEURISY ( 41 FDA reports)
PREMATURE LABOUR ( 41 FDA reports)
PROSTATE CANCER ( 41 FDA reports)
RADICULOPATHY ( 41 FDA reports)
ANAEMIA POSTOPERATIVE ( 40 FDA reports)
CATHETERISATION CARDIAC ( 40 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 40 FDA reports)
DILATATION ATRIAL ( 40 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 40 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 40 FDA reports)
LABYRINTHITIS ( 40 FDA reports)
LIGAMENT SPRAIN ( 40 FDA reports)
MITRAL VALVE CALCIFICATION ( 40 FDA reports)
MOTOR DYSFUNCTION ( 40 FDA reports)
MYOPATHY ( 40 FDA reports)
PLEURAL FIBROSIS ( 40 FDA reports)
PYELONEPHRITIS ( 40 FDA reports)
SCRATCH ( 40 FDA reports)
UROSEPSIS ( 40 FDA reports)
VAGINAL DISCHARGE ( 40 FDA reports)
SCHIZOPHRENIA ( 39 FDA reports)
TACHYPNOEA ( 39 FDA reports)
TEMPORAL ARTERITIS ( 39 FDA reports)
TOBACCO USER ( 39 FDA reports)
ACCIDENT ( 39 FDA reports)
ACTINOMYCOSIS ( 39 FDA reports)
ADRENAL NEOPLASM ( 39 FDA reports)
ANXIETY DISORDER ( 39 FDA reports)
ASBESTOSIS ( 39 FDA reports)
BARRETT'S OESOPHAGUS ( 39 FDA reports)
CHEILITIS ( 39 FDA reports)
COLITIS ISCHAEMIC ( 39 FDA reports)
DENTAL OPERATION ( 39 FDA reports)
GASTROINTESTINAL PAIN ( 39 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 39 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 39 FDA reports)
MUSCULOSKELETAL DISORDER ( 39 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 39 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 38 FDA reports)
CYSTITIS INTERSTITIAL ( 38 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 38 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 38 FDA reports)
HEART DISEASE CONGENITAL ( 38 FDA reports)
HOMICIDE ( 38 FDA reports)
HYPERTONIC BLADDER ( 38 FDA reports)
INJECTION SITE IRRITATION ( 38 FDA reports)
ISCHAEMIC STROKE ( 38 FDA reports)
KETOACIDOSIS ( 38 FDA reports)
MEDICATION RESIDUE ( 38 FDA reports)
PERSONALITY DISORDER ( 38 FDA reports)
TENSION ( 38 FDA reports)
RADIOTHERAPY ( 37 FDA reports)
STARING ( 37 FDA reports)
TRANSAMINASES INCREASED ( 37 FDA reports)
BILE DUCT STONE ( 37 FDA reports)
BLOOD CHLORIDE DECREASED ( 37 FDA reports)
BODY TEMPERATURE DECREASED ( 37 FDA reports)
COELIAC DISEASE ( 37 FDA reports)
GINGIVAL RECESSION ( 37 FDA reports)
GLYCOSURIA ( 37 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 37 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 37 FDA reports)
HUNGER ( 37 FDA reports)
INJECTION SITE RASH ( 37 FDA reports)
LIVER INJURY ( 37 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 37 FDA reports)
NASAL SEPTUM DEVIATION ( 37 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 37 FDA reports)
PARKINSONISM ( 37 FDA reports)
PELVIC FRACTURE ( 37 FDA reports)
POSTURE ABNORMAL ( 37 FDA reports)
AGORAPHOBIA ( 36 FDA reports)
BASEDOW'S DISEASE ( 36 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 36 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 36 FDA reports)
DYSPHORIA ( 36 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 36 FDA reports)
ERYTHEMA MULTIFORME ( 36 FDA reports)
FEELING DRUNK ( 36 FDA reports)
GALACTORRHOEA ( 36 FDA reports)
HIP ARTHROPLASTY ( 36 FDA reports)
HYPERTHYROIDISM ( 36 FDA reports)
HYPOALBUMINAEMIA ( 36 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 36 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 36 FDA reports)
MARROW HYPERPLASIA ( 36 FDA reports)
NICOTINE DEPENDENCE ( 36 FDA reports)
OPTIC NEURITIS ( 36 FDA reports)
POLYDIPSIA ( 36 FDA reports)
PROSTATE CANCER METASTATIC ( 36 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 36 FDA reports)
SUBDURAL HAEMATOMA ( 35 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 35 FDA reports)
TROPONIN INCREASED ( 35 FDA reports)
ACTINIC KERATOSIS ( 35 FDA reports)
APPENDICITIS ( 35 FDA reports)
BREAST CYST ( 35 FDA reports)
EAR DISCOMFORT ( 35 FDA reports)
EXTREMITY CONTRACTURE ( 35 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 35 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 35 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 35 FDA reports)
MOUTH HAEMORRHAGE ( 35 FDA reports)
MUSCLE DISORDER ( 35 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 35 FDA reports)
OESOPHAGEAL DISORDER ( 35 FDA reports)
ORAL HERPES ( 35 FDA reports)
PAIN OF SKIN ( 35 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 35 FDA reports)
PHOTOPSIA ( 35 FDA reports)
PROCTALGIA ( 35 FDA reports)
AREFLEXIA ( 34 FDA reports)
BLINDNESS TRANSIENT ( 34 FDA reports)
BLOOD CULTURE POSITIVE ( 34 FDA reports)
BONE NEOPLASM ( 34 FDA reports)
CAROTID ARTERY DISEASE ( 34 FDA reports)
CHROMATURIA ( 34 FDA reports)
CIRCULATORY COLLAPSE ( 34 FDA reports)
COLON CANCER ( 34 FDA reports)
DISSOCIATION ( 34 FDA reports)
EYE DISCHARGE ( 34 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 34 FDA reports)
IMPRISONMENT ( 34 FDA reports)
INGUINAL HERNIA ( 34 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 34 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 34 FDA reports)
LIPOMA ( 34 FDA reports)
MENINGIOMA ( 34 FDA reports)
METABOLIC ALKALOSIS ( 34 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 34 FDA reports)
RHONCHI ( 34 FDA reports)
THORACOTOMY ( 34 FDA reports)
URETHRAL DISORDER ( 34 FDA reports)
VIITH NERVE PARALYSIS ( 34 FDA reports)
SHOCK ( 33 FDA reports)
STENT PLACEMENT ( 33 FDA reports)
TONGUE COATED ( 33 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 33 FDA reports)
WALKING AID USER ( 33 FDA reports)
WEIGHT FLUCTUATION ( 33 FDA reports)
AGRANULOCYTOSIS ( 33 FDA reports)
ANAPHYLACTIC SHOCK ( 33 FDA reports)
ANORGASMIA ( 33 FDA reports)
BREAST RECONSTRUCTION ( 33 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 33 FDA reports)
EXTRASYSTOLES ( 33 FDA reports)
GASTROENTERITIS RADIATION ( 33 FDA reports)
GRANULOCYTOPENIA ( 33 FDA reports)
GYNAECOMASTIA ( 33 FDA reports)
HEPATOTOXICITY ( 33 FDA reports)
INTRAOCULAR LENS IMPLANT ( 33 FDA reports)
LEGAL PROBLEM ( 33 FDA reports)
MYOSITIS ( 33 FDA reports)
NEUTROPHIL COUNT INCREASED ( 33 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 33 FDA reports)
PARAESTHESIA ORAL ( 33 FDA reports)
PERONEAL NERVE PALSY ( 33 FDA reports)
PHOTOSENSITIVITY REACTION ( 33 FDA reports)
POLYP ( 33 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 33 FDA reports)
ABNORMAL FAECES ( 32 FDA reports)
AORTIC VALVE SCLEROSIS ( 32 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 32 FDA reports)
BRONCHITIS CHRONIC ( 32 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 32 FDA reports)
CATHETER PLACEMENT ( 32 FDA reports)
CHAPPED LIPS ( 32 FDA reports)
DENTAL PLAQUE ( 32 FDA reports)
DIZZINESS POSTURAL ( 32 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 32 FDA reports)
EMBOLISM ( 32 FDA reports)
EOSINOPHIL COUNT INCREASED ( 32 FDA reports)
HAEMATOCRIT INCREASED ( 32 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 32 FDA reports)
OESOPHAGEAL SPASM ( 32 FDA reports)
PAPILLOEDEMA ( 32 FDA reports)
PAROSMIA ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 32 FDA reports)
RECTOCELE ( 32 FDA reports)
RENAL TUBULAR NECROSIS ( 32 FDA reports)
SNORING ( 32 FDA reports)
TENDON DISORDER ( 32 FDA reports)
TENSION HEADACHE ( 32 FDA reports)
VENOUS THROMBOSIS ( 32 FDA reports)
VERTIGO POSITIONAL ( 32 FDA reports)
SARCOIDOSIS ( 31 FDA reports)
SYNOVITIS ( 31 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 31 FDA reports)
TREATMENT FAILURE ( 31 FDA reports)
UNDERDOSE ( 31 FDA reports)
ABSCESS ORAL ( 31 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 31 FDA reports)
BLADDER OPERATION ( 31 FDA reports)
BONE MARROW FAILURE ( 31 FDA reports)
BREATH SOUNDS ABNORMAL ( 31 FDA reports)
CARDIAC FLUTTER ( 31 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 31 FDA reports)
DYSMENORRHOEA ( 31 FDA reports)
EARLY SATIETY ( 31 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 31 FDA reports)
FORMICATION ( 31 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 31 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 31 FDA reports)
LIPASE INCREASED ( 31 FDA reports)
MEDICAL DEVICE COMPLICATION ( 31 FDA reports)
MELANOCYTIC NAEVUS ( 31 FDA reports)
PRIAPISM ( 31 FDA reports)
PULSE ABSENT ( 31 FDA reports)
ABDOMINAL TENDERNESS ( 30 FDA reports)
ANGIOPATHY ( 30 FDA reports)
BLOOD PRESSURE ABNORMAL ( 30 FDA reports)
BONE GRAFT ( 30 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 30 FDA reports)
CRANIOSYNOSTOSIS ( 30 FDA reports)
CYSTOCELE ( 30 FDA reports)
GRANULOMA ( 30 FDA reports)
HAEMORRHAGIC ANAEMIA ( 30 FDA reports)
MUSCLE CRAMP ( 30 FDA reports)
OCCULT BLOOD POSITIVE ( 30 FDA reports)
OTITIS EXTERNA ( 30 FDA reports)
PERFORMANCE STATUS DECREASED ( 30 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 30 FDA reports)
SKIN FIBROSIS ( 30 FDA reports)
SKIN HYPERPIGMENTATION ( 30 FDA reports)
THERMAL BURN ( 30 FDA reports)
TRIGEMINAL NEURALGIA ( 30 FDA reports)
WALKING DISABILITY ( 30 FDA reports)
WOUND INFECTION ( 30 FDA reports)
TEMPERATURE INTOLERANCE ( 29 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 29 FDA reports)
URGE INCONTINENCE ( 29 FDA reports)
VITH NERVE PARALYSIS ( 29 FDA reports)
ACUTE PRERENAL FAILURE ( 29 FDA reports)
ANOXIC ENCEPHALOPATHY ( 29 FDA reports)
APHAGIA ( 29 FDA reports)
ASTHENOPIA ( 29 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 29 FDA reports)
BRAIN HERNIATION ( 29 FDA reports)
BREAST DISCHARGE ( 29 FDA reports)
CREPITATIONS ( 29 FDA reports)
DEVELOPMENTAL DELAY ( 29 FDA reports)
DRUG ERUPTION ( 29 FDA reports)
HYPOPHOSPHATAEMIA ( 29 FDA reports)
IMPULSE-CONTROL DISORDER ( 29 FDA reports)
INADEQUATE ANALGESIA ( 29 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 29 FDA reports)
INJECTION SITE MASS ( 29 FDA reports)
NEOPLASM ( 29 FDA reports)
ORTHOPNOEA ( 29 FDA reports)
PERITONITIS ( 29 FDA reports)
POST HERPETIC NEURALGIA ( 29 FDA reports)
PROCEDURAL COMPLICATION ( 29 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 28 FDA reports)
ANAL FISSURE ( 28 FDA reports)
BACTERIAL DISEASE CARRIER ( 28 FDA reports)
BONE SWELLING ( 28 FDA reports)
CALCULUS URETERIC ( 28 FDA reports)
CAROTID BRUIT ( 28 FDA reports)
CERUMEN IMPACTION ( 28 FDA reports)
CHEST X-RAY ABNORMAL ( 28 FDA reports)
DEPERSONALISATION ( 28 FDA reports)
DEVICE BREAKAGE ( 28 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 28 FDA reports)
EYE OPERATION ( 28 FDA reports)
FIBRIN D DIMER INCREASED ( 28 FDA reports)
GANGRENE ( 28 FDA reports)
GINGIVAL ERYTHEMA ( 28 FDA reports)
HEARING IMPAIRED ( 28 FDA reports)
HYPOTONIA ( 28 FDA reports)
HYPOVENTILATION ( 28 FDA reports)
IMMUNE SYSTEM DISORDER ( 28 FDA reports)
INJECTION SITE BRUISING ( 28 FDA reports)
INJECTION SITE URTICARIA ( 28 FDA reports)
INTERMITTENT CLAUDICATION ( 28 FDA reports)
LIGAMENT INJURY ( 28 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 28 FDA reports)
PERIPHERAL ISCHAEMIA ( 28 FDA reports)
SEXUAL ABUSE ( 28 FDA reports)
SLUGGISHNESS ( 28 FDA reports)
STREPTOCOCCAL INFECTION ( 28 FDA reports)
SUBSTANCE ABUSE ( 28 FDA reports)
SEASONAL ALLERGY ( 27 FDA reports)
SENSATION OF FOREIGN BODY ( 27 FDA reports)
TONGUE INJURY ( 27 FDA reports)
TOOTH REPAIR ( 27 FDA reports)
VENOUS THROMBOSIS LIMB ( 27 FDA reports)
VISUAL FIELD DEFECT ( 27 FDA reports)
WHEELCHAIR USER ( 27 FDA reports)
ALCOHOL POISONING ( 27 FDA reports)
AUTOIMMUNE THYROIDITIS ( 27 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 27 FDA reports)
CANCER PAIN ( 27 FDA reports)
CARDIOGENIC SHOCK ( 27 FDA reports)
DROP ATTACKS ( 27 FDA reports)
ESCHERICHIA INFECTION ( 27 FDA reports)
ESSENTIAL TREMOR ( 27 FDA reports)
EYELID PTOSIS ( 27 FDA reports)
FISTULA DISCHARGE ( 27 FDA reports)
GASTRITIS EROSIVE ( 27 FDA reports)
HEMIPLEGIA ( 27 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 27 FDA reports)
HYPERNATRAEMIA ( 27 FDA reports)
LIP DRY ( 27 FDA reports)
MALIGNANT MELANOMA ( 27 FDA reports)
PARTNER STRESS ( 27 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 27 FDA reports)
POSTICTAL STATE ( 27 FDA reports)
ABORTION INDUCED ( 26 FDA reports)
ABSCESS JAW ( 26 FDA reports)
BIPOLAR II DISORDER ( 26 FDA reports)
COMMUNICATION DISORDER ( 26 FDA reports)
CORONARY ARTERY STENOSIS ( 26 FDA reports)
DEAFNESS NEUROSENSORY ( 26 FDA reports)
DEPRESSION SUICIDAL ( 26 FDA reports)
DIABETIC GASTROPARESIS ( 26 FDA reports)
DUODENITIS ( 26 FDA reports)
DYSTHYMIC DISORDER ( 26 FDA reports)
FRACTURE NONUNION ( 26 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 26 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 26 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 26 FDA reports)
HEPATIC LESION ( 26 FDA reports)
HILAR LYMPHADENOPATHY ( 26 FDA reports)
HYPERCOAGULATION ( 26 FDA reports)
HYPERMETABOLISM ( 26 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 26 FDA reports)
INJECTION SITE DISCOLOURATION ( 26 FDA reports)
INTRACRANIAL ANEURYSM ( 26 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 26 FDA reports)
METABOLIC DISORDER ( 26 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 26 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 26 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 26 FDA reports)
PULMONARY THROMBOSIS ( 26 FDA reports)
SACROILIITIS ( 26 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 26 FDA reports)
SINUS OPERATION ( 26 FDA reports)
THYROID CANCER ( 26 FDA reports)
TORTICOLLIS ( 26 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 26 FDA reports)
RADIUS FRACTURE ( 25 FDA reports)
REFLUX GASTRITIS ( 25 FDA reports)
RENAL ARTERY STENOSIS ( 25 FDA reports)
RETINAL TEAR ( 25 FDA reports)
SCAB ( 25 FDA reports)
SLEEP TALKING ( 25 FDA reports)
VAGINITIS BACTERIAL ( 25 FDA reports)
VULVOVAGINAL PRURITUS ( 25 FDA reports)
ALCOHOL ABUSE ( 25 FDA reports)
AORTIC VALVE DISEASE ( 25 FDA reports)
BLOOD DISORDER ( 25 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 25 FDA reports)
CLEFT PALATE ( 25 FDA reports)
DECREASED ACTIVITY ( 25 FDA reports)
DEMYELINATION ( 25 FDA reports)
FACE OEDEMA ( 25 FDA reports)
FLUID INTAKE REDUCED ( 25 FDA reports)
GINGIVAL OPERATION ( 25 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HALLUCINATIONS, MIXED ( 25 FDA reports)
HERNIA REPAIR ( 25 FDA reports)
LIBIDO INCREASED ( 25 FDA reports)
LIFE EXPECTANCY SHORTENED ( 25 FDA reports)
LIGAMENT RUPTURE ( 25 FDA reports)
LIP DISCOLOURATION ( 25 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 25 FDA reports)
METABOLIC ENCEPHALOPATHY ( 25 FDA reports)
ORAL DISCOMFORT ( 25 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 25 FDA reports)
RADIATION INJURY ( 25 FDA reports)
ACCIDENTAL DEATH ( 24 FDA reports)
APHONIA ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK ( 24 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 24 FDA reports)
BRAIN DEATH ( 24 FDA reports)
CALCINOSIS ( 24 FDA reports)
CEREBRAL DISORDER ( 24 FDA reports)
CLUMSINESS ( 24 FDA reports)
CONDUCTION DISORDER ( 24 FDA reports)
CORONARY ARTERY BYPASS ( 24 FDA reports)
DEVICE OCCLUSION ( 24 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 24 FDA reports)
EYE MOVEMENT DISORDER ( 24 FDA reports)
FOLLICULITIS ( 24 FDA reports)
FRACTURE ( 24 FDA reports)
HYPERTENSIVE HEART DISEASE ( 24 FDA reports)
LARGE INTESTINAL ULCER ( 24 FDA reports)
MASTECTOMY ( 24 FDA reports)
MUCOSAL ULCERATION ( 24 FDA reports)
MUSCLE CONTRACTURE ( 24 FDA reports)
NASAL DISORDER ( 24 FDA reports)
NEURODERMATITIS ( 24 FDA reports)
OCULAR ICTERUS ( 24 FDA reports)
OROANTRAL FISTULA ( 24 FDA reports)
PERIORBITAL OEDEMA ( 24 FDA reports)
POLYMYALGIA RHEUMATICA ( 24 FDA reports)
PSYCHIATRIC SYMPTOM ( 24 FDA reports)
PYELOCALIECTASIS ( 24 FDA reports)
RASH PUSTULAR ( 24 FDA reports)
RECTAL ABSCESS ( 24 FDA reports)
RETINAL DETACHMENT ( 24 FDA reports)
RETINOPATHY ( 24 FDA reports)
SALIVARY HYPERSECRETION ( 24 FDA reports)
SKIN IRRITATION ( 24 FDA reports)
SPINAL OPERATION ( 24 FDA reports)
STRESS SYMPTOMS ( 24 FDA reports)
STUPOR ( 24 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 24 FDA reports)
TACHYPHRENIA ( 24 FDA reports)
TERMINAL INSOMNIA ( 24 FDA reports)
THROMBOSIS IN DEVICE ( 24 FDA reports)
URINARY HESITATION ( 24 FDA reports)
WOUND SECRETION ( 24 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 23 FDA reports)
SCOTOMA ( 23 FDA reports)
SKIN REACTION ( 23 FDA reports)
SLEEP TERROR ( 23 FDA reports)
SPINAL FUSION SURGERY ( 23 FDA reports)
STATUS EPILEPTICUS ( 23 FDA reports)
TENOSYNOVITIS STENOSANS ( 23 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 23 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 23 FDA reports)
WEIGHT BEARING DIFFICULTY ( 23 FDA reports)
ABDOMINAL ADHESIONS ( 23 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 23 FDA reports)
ANIMAL BITE ( 23 FDA reports)
BLADDER CANCER ( 23 FDA reports)
CAROTID ARTERY OCCLUSION ( 23 FDA reports)
CARTILAGE INJURY ( 23 FDA reports)
CATHETER RELATED INFECTION ( 23 FDA reports)
COLLAPSE OF LUNG ( 23 FDA reports)
DUODENAL ULCER ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 23 FDA reports)
ENDOCARDITIS ( 23 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 23 FDA reports)
FRACTURE DELAYED UNION ( 23 FDA reports)
HEART INJURY ( 23 FDA reports)
HEPATIC ENCEPHALOPATHY ( 23 FDA reports)
HYDROCEPHALUS ( 23 FDA reports)
HYDROPNEUMOTHORAX ( 23 FDA reports)
HYPERACUSIS ( 23 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 23 FDA reports)
JOINT CONTRACTURE ( 23 FDA reports)
KNEE OPERATION ( 23 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 23 FDA reports)
PERIARTHRITIS ( 23 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 23 FDA reports)
PRODUCT ADHESION ISSUE ( 23 FDA reports)
ABNORMAL SENSATION IN EYE ( 22 FDA reports)
ACIDOSIS ( 22 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 22 FDA reports)
AORTIC VALVE STENOSIS ( 22 FDA reports)
APGAR SCORE LOW ( 22 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 22 FDA reports)
BENIGN BREAST NEOPLASM ( 22 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 22 FDA reports)
BRAIN INJURY ( 22 FDA reports)
CARDIAC PACEMAKER INSERTION ( 22 FDA reports)
ENCEPHALOMALACIA ( 22 FDA reports)
IMMUNOSUPPRESSION ( 22 FDA reports)
ISCHAEMIA ( 22 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 22 FDA reports)
MONOCLONAL GAMMOPATHY ( 22 FDA reports)
MONOCYTE COUNT INCREASED ( 22 FDA reports)
NEUROLOGICAL SYMPTOM ( 22 FDA reports)
OVARIAN CANCER ( 22 FDA reports)
PERIORBITAL HAEMATOMA ( 22 FDA reports)
PITTING OEDEMA ( 22 FDA reports)
PULMONARY HAEMORRHAGE ( 22 FDA reports)
SCARLET FEVER ( 22 FDA reports)
STEM CELL TRANSPLANT ( 22 FDA reports)
TELANGIECTASIA ( 22 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 22 FDA reports)
THROMBOCYTOSIS ( 22 FDA reports)
VASCULAR ANOMALY ( 22 FDA reports)
RECTAL FISSURE ( 21 FDA reports)
SELF ESTEEM DECREASED ( 21 FDA reports)
SKIN WARM ( 21 FDA reports)
STREPTOCOCCAL SEPSIS ( 21 FDA reports)
TALIPES ( 21 FDA reports)
TINEA PEDIS ( 21 FDA reports)
TRAUMATIC BRAIN INJURY ( 21 FDA reports)
UTERINE POLYP ( 21 FDA reports)
VASCULAR PSEUDOANEURYSM ( 21 FDA reports)
VENTRICULAR DYSFUNCTION ( 21 FDA reports)
VOCAL CORD PARALYSIS ( 21 FDA reports)
ACETABULUM FRACTURE ( 21 FDA reports)
ACUTE PSYCHOSIS ( 21 FDA reports)
APPLICATION SITE IRRITATION ( 21 FDA reports)
ARTHROPOD BITE ( 21 FDA reports)
BELLIGERENCE ( 21 FDA reports)
BLEPHAROSPASM ( 21 FDA reports)
BONE CYST ( 21 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 21 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 21 FDA reports)
COLON ADENOMA ( 21 FDA reports)
CORONARY ANGIOPLASTY ( 21 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 21 FDA reports)
DRUG LEVEL DECREASED ( 21 FDA reports)
DYSGRAPHIA ( 21 FDA reports)
EFFUSION ( 21 FDA reports)
EYE ROLLING ( 21 FDA reports)
EYELID OEDEMA ( 21 FDA reports)
FAECALOMA ( 21 FDA reports)
FEELING GUILTY ( 21 FDA reports)
FOAMING AT MOUTH ( 21 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 21 FDA reports)
HYPERREFLEXIA ( 21 FDA reports)
INCISIONAL DRAINAGE ( 21 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 21 FDA reports)
JUGULAR VEIN THROMBOSIS ( 21 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 21 FDA reports)
LUNG CONSOLIDATION ( 21 FDA reports)
LYMPHADENITIS ( 21 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 21 FDA reports)
METASTASES TO ADRENALS ( 21 FDA reports)
METASTASES TO THORAX ( 21 FDA reports)
METASTATIC NEOPLASM ( 21 FDA reports)
MUMPS ( 21 FDA reports)
NONSPECIFIC REACTION ( 21 FDA reports)
OVERWEIGHT ( 21 FDA reports)
PANCREATIC CARCINOMA ( 21 FDA reports)
PANCREATIC DISORDER ( 21 FDA reports)
PATELLA FRACTURE ( 21 FDA reports)
PERIRECTAL ABSCESS ( 21 FDA reports)
PERITONEAL DISORDER ( 21 FDA reports)
PROSTATIC DISORDER ( 21 FDA reports)
PSORIATIC ARTHROPATHY ( 21 FDA reports)
PURPURA ( 21 FDA reports)
ABDOMINAL SEPSIS ( 20 FDA reports)
ADRENAL DISORDER ( 20 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 20 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 20 FDA reports)
BLOOD BICARBONATE DECREASED ( 20 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 20 FDA reports)
BRONCHOPLEURAL FISTULA ( 20 FDA reports)
CEREBRAL THROMBOSIS ( 20 FDA reports)
CHOKING SENSATION ( 20 FDA reports)
CHOREA ( 20 FDA reports)
CONJUNCTIVITIS ( 20 FDA reports)
DIABETIC FOOT ( 20 FDA reports)
DIVORCED ( 20 FDA reports)
EARLY MORNING AWAKENING ( 20 FDA reports)
ENTEROCOCCAL INFECTION ( 20 FDA reports)
FEAR OF DEATH ( 20 FDA reports)
FOOD INTOLERANCE ( 20 FDA reports)
GALLBLADDER OPERATION ( 20 FDA reports)
GINGIVAL EROSION ( 20 FDA reports)
HANGOVER ( 20 FDA reports)
INDIFFERENCE ( 20 FDA reports)
INJECTION SITE NODULE ( 20 FDA reports)
INTRACARDIAC THROMBUS ( 20 FDA reports)
LOSS OF CONTROL OF LEGS ( 20 FDA reports)
MENOPAUSAL SYMPTOMS ( 20 FDA reports)
METASTATIC PAIN ( 20 FDA reports)
MIOSIS ( 20 FDA reports)
MITRAL VALVE SCLEROSIS ( 20 FDA reports)
NARCOLEPSY ( 20 FDA reports)
NARCOTIC INTOXICATION ( 20 FDA reports)
NEGATIVE THOUGHTS ( 20 FDA reports)
NERVE COMPRESSION ( 20 FDA reports)
ONYCHOCLASIS ( 20 FDA reports)
ORAL NEOPLASM ( 20 FDA reports)
PCO2 DECREASED ( 20 FDA reports)
PSEUDOMONAS INFECTION ( 20 FDA reports)
PSYCHOLOGICAL TRAUMA ( 20 FDA reports)
SMALL INTESTINE OPERATION ( 20 FDA reports)
TONGUE BITING ( 20 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 20 FDA reports)
URETHRAL STENOSIS ( 20 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 20 FDA reports)
WEIGHT LOSS POOR ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
WRONG DRUG ADMINISTERED ( 20 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 19 FDA reports)
RETINAL DISORDER ( 19 FDA reports)
RUBELLA ( 19 FDA reports)
SIMPLE PARTIAL SEIZURES ( 19 FDA reports)
SKIN PLAQUE ( 19 FDA reports)
SPINAL DECOMPRESSION ( 19 FDA reports)
SPONDYLOLYSIS ( 19 FDA reports)
THERAPY CESSATION ( 19 FDA reports)
URETERAL DISORDER ( 19 FDA reports)
VARICES OESOPHAGEAL ( 19 FDA reports)
VASCULAR INSUFFICIENCY ( 19 FDA reports)
VENTRICULAR HYPOKINESIA ( 19 FDA reports)
VIRAL LOAD INCREASED ( 19 FDA reports)
ALVEOLOPLASTY ( 19 FDA reports)
AMBLYOPIA ( 19 FDA reports)
ANAL FISTULA ( 19 FDA reports)
ASTERIXIS ( 19 FDA reports)
ATROPHIC VULVOVAGINITIS ( 19 FDA reports)
BILIARY DILATATION ( 19 FDA reports)
BIOPSY ( 19 FDA reports)
BLADDER NEOPLASM ( 19 FDA reports)
BLOOD COUNT ABNORMAL ( 19 FDA reports)
BREAST ENLARGEMENT ( 19 FDA reports)
BREAST SWELLING ( 19 FDA reports)
CARDIAC ENZYMES INCREASED ( 19 FDA reports)
CHEMICAL POISONING ( 19 FDA reports)
CHRONIC FATIGUE SYNDROME ( 19 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 19 FDA reports)
CLOSTRIDIUM COLITIS ( 19 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 19 FDA reports)
DRUG TOLERANCE ( 19 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 19 FDA reports)
ENTERITIS ( 19 FDA reports)
FULL BLOOD COUNT DECREASED ( 19 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 19 FDA reports)
HAEMOLYSIS ( 19 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 19 FDA reports)
HEPATIC CONGESTION ( 19 FDA reports)
HYPOPNOEA ( 19 FDA reports)
ILEAL STENOSIS ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
JUDGEMENT IMPAIRED ( 19 FDA reports)
LICHENOID KERATOSIS ( 19 FDA reports)
LIP PAIN ( 19 FDA reports)
LUPUS-LIKE SYNDROME ( 19 FDA reports)
MICROCYTIC ANAEMIA ( 19 FDA reports)
MICTURITION DISORDER ( 19 FDA reports)
MONOPLEGIA ( 19 FDA reports)
NASAL DISCOMFORT ( 19 FDA reports)
PAINFUL ERECTION ( 19 FDA reports)
PAINFUL RESPIRATION ( 19 FDA reports)
PULMONARY RADIATION INJURY ( 19 FDA reports)
PUPIL FIXED ( 19 FDA reports)
PYURIA ( 19 FDA reports)
ABDOMINAL ABSCESS ( 18 FDA reports)
ACCOMMODATION DISORDER ( 18 FDA reports)
ACUTE HEPATIC FAILURE ( 18 FDA reports)
ADHESION ( 18 FDA reports)
ASPIRATION JOINT ( 18 FDA reports)
BLOOD ALCOHOL INCREASED ( 18 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 18 FDA reports)
BLOOD UREA DECREASED ( 18 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 18 FDA reports)
BREAST HYPERPLASIA ( 18 FDA reports)
BRONCHOPNEUMONIA ( 18 FDA reports)
BUNION ( 18 FDA reports)
CATATONIA ( 18 FDA reports)
COLONOSCOPY ( 18 FDA reports)
CONVULSION NEONATAL ( 18 FDA reports)
DISSOCIATIVE DISORDER ( 18 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 18 FDA reports)
EDUCATIONAL PROBLEM ( 18 FDA reports)
EYE INJURY ( 18 FDA reports)
EYE LASER SURGERY ( 18 FDA reports)
FOOT OPERATION ( 18 FDA reports)
GALLBLADDER PAIN ( 18 FDA reports)
GASTRIC HAEMORRHAGE ( 18 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 18 FDA reports)
HEART RATE ABNORMAL ( 18 FDA reports)
HEAT STROKE ( 18 FDA reports)
HEPATITIS B ( 18 FDA reports)
HERPES VIRUS INFECTION ( 18 FDA reports)
HYDROCELE ( 18 FDA reports)
HYPERPROLACTINAEMIA ( 18 FDA reports)
IMPAIRED FASTING GLUCOSE ( 18 FDA reports)
INFARCTION ( 18 FDA reports)
INJURY CORNEAL ( 18 FDA reports)
JOINT ARTHROPLASTY ( 18 FDA reports)
JOINT LOCK ( 18 FDA reports)
KERATITIS ( 18 FDA reports)
KLEBSIELLA INFECTION ( 18 FDA reports)
LACTOSE INTOLERANCE ( 18 FDA reports)
MASTITIS ( 18 FDA reports)
METASTASES TO SKIN ( 18 FDA reports)
MORTON'S NEUROMA ( 18 FDA reports)
NASAL DRYNESS ( 18 FDA reports)
NEPHROPATHY ( 18 FDA reports)
NERVE ROOT LESION ( 18 FDA reports)
PARONYCHIA ( 18 FDA reports)
PENIS DEVIATION ( 18 FDA reports)
PERIODONTAL DESTRUCTION ( 18 FDA reports)
PRESBYOPIA ( 18 FDA reports)
PROSTATITIS ( 18 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 18 FDA reports)
RENAL ATROPHY ( 18 FDA reports)
RENAL MASS ( 18 FDA reports)
ROTATOR CUFF REPAIR ( 18 FDA reports)
SELF MUTILATION ( 18 FDA reports)
SKIN SWELLING ( 18 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 18 FDA reports)
TOOTH DEPOSIT ( 18 FDA reports)
TRANSFUSION ( 18 FDA reports)
UMBILICAL CORD AROUND NECK ( 18 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 18 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 17 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 17 FDA reports)
SEBORRHOEIC DERMATITIS ( 17 FDA reports)
SICK SINUS SYNDROME ( 17 FDA reports)
SPUTUM DISCOLOURED ( 17 FDA reports)
SUBDURAL HAEMORRHAGE ( 17 FDA reports)
SYNCOPE VASOVAGAL ( 17 FDA reports)
THROMBOPHLEBITIS ( 17 FDA reports)
TONGUE DISCOLOURATION ( 17 FDA reports)
TONIC CLONIC MOVEMENTS ( 17 FDA reports)
UMBILICAL CORD ABNORMALITY ( 17 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 17 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
APPLICATION SITE VESICLES ( 17 FDA reports)
BIOPSY BREAST ( 17 FDA reports)
BLOOD CHLORIDE INCREASED ( 17 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 17 FDA reports)
BONE MARROW DISORDER ( 17 FDA reports)
BRAIN NEOPLASM ( 17 FDA reports)
BREAKTHROUGH PAIN ( 17 FDA reports)
CATARACT NUCLEAR ( 17 FDA reports)
CHEST WALL MASS ( 17 FDA reports)
CHEST WALL PAIN ( 17 FDA reports)
COCCYDYNIA ( 17 FDA reports)
CULTURE URINE POSITIVE ( 17 FDA reports)
DEVICE LEAKAGE ( 17 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 17 FDA reports)
DYSPAREUNIA ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 17 FDA reports)
EMBOLIC STROKE ( 17 FDA reports)
EMPYEMA ( 17 FDA reports)
ENURESIS ( 17 FDA reports)
FEEDING DISORDER NEONATAL ( 17 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
IMPATIENCE ( 17 FDA reports)
INCISIONAL HERNIA ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
MACROCYTOSIS ( 17 FDA reports)
MALOCCLUSION ( 17 FDA reports)
MAMMOPLASTY ( 17 FDA reports)
MENINGITIS ( 17 FDA reports)
MENISCUS REMOVAL ( 17 FDA reports)
NECK MASS ( 17 FDA reports)
NEUROGENIC BLADDER ( 17 FDA reports)
NON-SMALL CELL LUNG CANCER ( 17 FDA reports)
ORAL MUCOSA ATROPHY ( 17 FDA reports)
ORGAN FAILURE ( 17 FDA reports)
PELVIC HAEMATOMA ( 17 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 17 FDA reports)
PERINEURIAL CYST ( 17 FDA reports)
PHLEBITIS ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 16 FDA reports)
ACROCHORDON ( 16 FDA reports)
ADENOCARCINOMA ( 16 FDA reports)
ADENOMYOSIS ( 16 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 16 FDA reports)
ANGIOFIBROMA ( 16 FDA reports)
ANGIONEUROTIC OEDEMA ( 16 FDA reports)
ANORECTAL DISCOMFORT ( 16 FDA reports)
APLASTIC ANAEMIA ( 16 FDA reports)
APPLICATION SITE RASH ( 16 FDA reports)
ARTERIAL INSUFFICIENCY ( 16 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 16 FDA reports)
ASPIRATION PLEURAL CAVITY ( 16 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 16 FDA reports)
BACTERIAL SEPSIS ( 16 FDA reports)
BLEPHARITIS ( 16 FDA reports)
BLOOD PH INCREASED ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 16 FDA reports)
CAECITIS ( 16 FDA reports)
CATHETER REMOVAL ( 16 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 16 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 16 FDA reports)
CLUSTER HEADACHE ( 16 FDA reports)
COMPULSIONS ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
CYANOSIS NEONATAL ( 16 FDA reports)
DERMATITIS ACNEIFORM ( 16 FDA reports)
DISTRACTIBILITY ( 16 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
DYSTROPHIC CALCIFICATION ( 16 FDA reports)
ENCEPHALITIS ( 16 FDA reports)
FACIAL PARESIS ( 16 FDA reports)
FEELINGS OF WORTHLESSNESS ( 16 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 16 FDA reports)
HAEMOGLOBIN INCREASED ( 16 FDA reports)
HELICOBACTER GASTRITIS ( 16 FDA reports)
HEPATIC MASS ( 16 FDA reports)
HORNER'S SYNDROME ( 16 FDA reports)
HYPERTENSIVE CRISIS ( 16 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 16 FDA reports)
INTESTINAL POLYP ( 16 FDA reports)
LENTIGO ( 16 FDA reports)
LEUKAEMIA ( 16 FDA reports)
LYME DISEASE ( 16 FDA reports)
MACULOPATHY ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 16 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 16 FDA reports)
NODAL OSTEOARTHRITIS ( 16 FDA reports)
OESOPHAGEAL STENOSIS ( 16 FDA reports)
ORTHOSIS USER ( 16 FDA reports)
PALATAL DISORDER ( 16 FDA reports)
PANCREATITIS RELAPSING ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
PHOTODERMATOSIS ( 16 FDA reports)
POSTNASAL DRIP ( 16 FDA reports)
POSTPARTUM DEPRESSION ( 16 FDA reports)
PRE-ECLAMPSIA ( 16 FDA reports)
PROTEIN TOTAL DECREASED ( 16 FDA reports)
PROTEIN TOTAL INCREASED ( 16 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 16 FDA reports)
RADICULITIS ( 16 FDA reports)
READING DISORDER ( 16 FDA reports)
REGURGITATION ( 16 FDA reports)
RESPIRATORY DEPRESSION ( 16 FDA reports)
SHOULDER PAIN ( 16 FDA reports)
SIGMOIDITIS ( 16 FDA reports)
SINUS POLYP ( 16 FDA reports)
SPINA BIFIDA ( 16 FDA reports)
TORSADE DE POINTES ( 16 FDA reports)
TRIGGER FINGER ( 16 FDA reports)
TUNNEL VISION ( 16 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 16 FDA reports)
RESORPTION BONE INCREASED ( 15 FDA reports)
SJOGREN'S SYNDROME ( 15 FDA reports)
STRABISMUS ( 15 FDA reports)
SUTURE RELATED COMPLICATION ( 15 FDA reports)
THROAT LESION ( 15 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
TOE AMPUTATION ( 15 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 15 FDA reports)
TRACHEOBRONCHITIS ( 15 FDA reports)
UTERINE ENLARGEMENT ( 15 FDA reports)
VASCULAR CALCIFICATION ( 15 FDA reports)
VERTEBRAL WEDGING ( 15 FDA reports)
YELLOW SKIN ( 15 FDA reports)
ABDOMINAL MASS ( 15 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 15 FDA reports)
ACCIDENTAL EXPOSURE ( 15 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
ADRENAL INSUFFICIENCY ( 15 FDA reports)
AUTONOMIC NEUROPATHY ( 15 FDA reports)
BLOOD CORTISOL ABNORMAL ( 15 FDA reports)
BLOOD URIC ACID INCREASED ( 15 FDA reports)
BLOODY DISCHARGE ( 15 FDA reports)
BONE EROSION ( 15 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 15 FDA reports)
BREAST CALCIFICATIONS ( 15 FDA reports)
BREAST CANCER IN SITU ( 15 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 15 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 15 FDA reports)
CEREBELLAR HAEMORRHAGE ( 15 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 15 FDA reports)
CHEST WALL OPERATION ( 15 FDA reports)
COLONIC OBSTRUCTION ( 15 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 15 FDA reports)
CONNECTIVE TISSUE DISORDER ( 15 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 15 FDA reports)
DEAFNESS UNILATERAL ( 15 FDA reports)
ECZEMA ASTEATOTIC ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 15 FDA reports)
ENDOTRACHEAL INTUBATION ( 15 FDA reports)
GASTRIC BYPASS ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
HAIR COLOUR CHANGES ( 15 FDA reports)
HEAD DISCOMFORT ( 15 FDA reports)
HEPATIC ENZYME ABNORMAL ( 15 FDA reports)
HORMONE LEVEL ABNORMAL ( 15 FDA reports)
HYPERCAPNIA ( 15 FDA reports)
HYPOREFLEXIA ( 15 FDA reports)
HYPOTRICHOSIS ( 15 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
INJECTION SITE WARMTH ( 15 FDA reports)
INTRA-UTERINE DEATH ( 15 FDA reports)
MENSTRUAL DISORDER ( 15 FDA reports)
OBSTRUCTION ( 15 FDA reports)
ORAL FUNGAL INFECTION ( 15 FDA reports)
OTITIS MEDIA CHRONIC ( 15 FDA reports)
OVARIAN MASS ( 15 FDA reports)
PANCREATIC INSUFFICIENCY ( 15 FDA reports)
PARTIAL SEIZURES ( 15 FDA reports)
PHARYNGEAL ERYTHEMA ( 15 FDA reports)
PLASMINOGEN ACTIVATOR INHIBITOR ( 15 FDA reports)
PLASTIC SURGERY ( 15 FDA reports)
PNEUMATOSIS INTESTINALIS ( 15 FDA reports)
POISONING ( 15 FDA reports)
POLYCYSTIC OVARIES ( 15 FDA reports)
POLYMEDICATION ( 15 FDA reports)
POOR VENOUS ACCESS ( 15 FDA reports)
PRIMARY HYPOGONADISM ( 15 FDA reports)
PROSTATE CANCER RECURRENT ( 15 FDA reports)
PROTEIN URINE PRESENT ( 15 FDA reports)
ACTIVATION SYNDROME ( 14 FDA reports)
AMMONIA INCREASED ( 14 FDA reports)
ANAL HAEMORRHAGE ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 14 FDA reports)
AORTIC VALVE CALCIFICATION ( 14 FDA reports)
APPLICATION SITE PAIN ( 14 FDA reports)
APPLICATION SITE REACTION ( 14 FDA reports)
BURNS THIRD DEGREE ( 14 FDA reports)
CARDIAC ASTHMA ( 14 FDA reports)
CEREBRAL ARTERY STENOSIS ( 14 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 14 FDA reports)
COARCTATION OF THE AORTA ( 14 FDA reports)
EAR HAEMORRHAGE ( 14 FDA reports)
EJACULATION FAILURE ( 14 FDA reports)
ENDOMETRIOSIS ( 14 FDA reports)
ERECTION INCREASED ( 14 FDA reports)
ESSENTIAL HYPERTENSION ( 14 FDA reports)
FACIAL SPASM ( 14 FDA reports)
FALLOT'S TETRALOGY ( 14 FDA reports)
FIBROUS HISTIOCYTOMA ( 14 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 14 FDA reports)
FUNGAEMIA ( 14 FDA reports)
GRIMACING ( 14 FDA reports)
HAIR TEXTURE ABNORMAL ( 14 FDA reports)
HEPATIC FIBROSIS ( 14 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 14 FDA reports)
ICHTHYOSIS ( 14 FDA reports)
INFUSION SITE ERYTHEMA ( 14 FDA reports)
INJECTION SITE BURNING ( 14 FDA reports)
INJECTION SITE INDURATION ( 14 FDA reports)
INSULIN RESISTANCE ( 14 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 14 FDA reports)
IRITIS ( 14 FDA reports)
IRON DEFICIENCY ( 14 FDA reports)
IUCD COMPLICATION ( 14 FDA reports)
LABILE HYPERTENSION ( 14 FDA reports)
LOGORRHOEA ( 14 FDA reports)
MACULAR OEDEMA ( 14 FDA reports)
MALABSORPTION ( 14 FDA reports)
METASTASIS ( 14 FDA reports)
MITRAL VALVE DISEASE ( 14 FDA reports)
MYELITIS TRANSVERSE ( 14 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
NYSTAGMUS ( 14 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 14 FDA reports)
OESOPHAGEAL PAIN ( 14 FDA reports)
OESOPHAGEAL ULCER ( 14 FDA reports)
OLIGURIA ( 14 FDA reports)
OOPHORECTOMY ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
ORTHODONTIC APPLIANCE USER ( 14 FDA reports)
OSTEOCHONDROSIS ( 14 FDA reports)
PERICARDIAL DISEASE ( 14 FDA reports)
PHARYNGEAL DISORDER ( 14 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 14 FDA reports)
POST THROMBOTIC SYNDROME ( 14 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
PULMONARY GRANULOMA ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 14 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 14 FDA reports)
SERRATIA BACTERAEMIA ( 14 FDA reports)
SKIN EROSION ( 14 FDA reports)
SPONTANEOUS PENILE ERECTION ( 14 FDA reports)
TINEA CRURIS ( 14 FDA reports)
TONSILLITIS ( 14 FDA reports)
TUBERCULOSIS ( 14 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 14 FDA reports)
ULCER HAEMORRHAGE ( 14 FDA reports)
UNINTENDED PREGNANCY ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
URINE ODOUR ABNORMAL ( 14 FDA reports)
UTERINE DISORDER ( 14 FDA reports)
UVEITIS ( 14 FDA reports)
VASODILATATION ( 14 FDA reports)
WOUND HAEMORRHAGE ( 14 FDA reports)
YAWNING ( 14 FDA reports)
RECURRENT CANCER ( 13 FDA reports)
REFLUX LARYNGITIS ( 13 FDA reports)
RETROPERITONEAL HAEMATOMA ( 13 FDA reports)
RIGHT ATRIAL DILATATION ( 13 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 13 FDA reports)
SENSATION OF PRESSURE ( 13 FDA reports)
SERUM SICKNESS ( 13 FDA reports)
SKIN GRAFT ( 13 FDA reports)
SKIN NODULE ( 13 FDA reports)
SOFT TISSUE INJURY ( 13 FDA reports)
SPINAL CORD DISORDER ( 13 FDA reports)
SUDDEN ONSET OF SLEEP ( 13 FDA reports)
TRAUMATIC HAEMATOMA ( 13 FDA reports)
TUMOUR INVASION ( 13 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 13 FDA reports)
URINE OUTPUT INCREASED ( 13 FDA reports)
VENOUS STENOSIS ( 13 FDA reports)
VITAMIN B12 INCREASED ( 13 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
ALVEOLITIS ALLERGIC ( 13 FDA reports)
AORTIC DISORDER ( 13 FDA reports)
APPENDICITIS PERFORATED ( 13 FDA reports)
ARTERIAL DISORDER ( 13 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 13 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 13 FDA reports)
BLOOD PH DECREASED ( 13 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 13 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
BRADYPHRENIA ( 13 FDA reports)
BRAIN MASS ( 13 FDA reports)
CARBON DIOXIDE DECREASED ( 13 FDA reports)
CARDIAC OUTPUT DECREASED ( 13 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 13 FDA reports)
CATHETER RELATED COMPLICATION ( 13 FDA reports)
CEREBELLAR INFARCTION ( 13 FDA reports)
CERVICAL SPINE FLATTENING ( 13 FDA reports)
CHOLESTEROSIS ( 13 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 13 FDA reports)
COMMINUTED FRACTURE ( 13 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 13 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 13 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 13 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 13 FDA reports)
DRY THROAT ( 13 FDA reports)
DYSAESTHESIA ( 13 FDA reports)
ENTEROCUTANEOUS FISTULA ( 13 FDA reports)
EOSINOPHILIA ( 13 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 13 FDA reports)
FOETAL GROWTH RETARDATION ( 13 FDA reports)
GAMBLING ( 13 FDA reports)
GINGIVAL OEDEMA ( 13 FDA reports)
HAEMOTHORAX ( 13 FDA reports)
HEPATIC PAIN ( 13 FDA reports)
HEPATITIS CHOLESTATIC ( 13 FDA reports)
HYPERTONIA ( 13 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 13 FDA reports)
INCORRECT STORAGE OF DRUG ( 13 FDA reports)
INFANTILE APNOEIC ATTACK ( 13 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 13 FDA reports)
INJECTION SITE EXTRAVASATION ( 13 FDA reports)
KERATOMILEUSIS ( 13 FDA reports)
LISTLESS ( 13 FDA reports)
LIVER TRANSPLANT ( 13 FDA reports)
LOCALISED OEDEMA ( 13 FDA reports)
MEDICAL DEVICE REMOVAL ( 13 FDA reports)
MYELOPATHY ( 13 FDA reports)
MYOPIA ( 13 FDA reports)
NECROSIS ( 13 FDA reports)
NEPHROSCLEROSIS ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
OBSTRUCTIVE UROPATHY ( 13 FDA reports)
OTITIS MEDIA ACUTE ( 13 FDA reports)
PARAPLEGIA ( 13 FDA reports)
PAROTITIS ( 13 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 13 FDA reports)
PELVIC FLUID COLLECTION ( 13 FDA reports)
PELVIC MUSCLES INADEQUATE ( 13 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 13 FDA reports)
PIGMENTATION DISORDER ( 13 FDA reports)
PLASMACYTOMA ( 13 FDA reports)
POOR DENTAL CONDITION ( 13 FDA reports)
POSTOPERATIVE ILEUS ( 13 FDA reports)
PROCTITIS ( 13 FDA reports)
ABSCESS NECK ( 12 FDA reports)
ACCIDENT AT WORK ( 12 FDA reports)
ADNEXA UTERI CYST ( 12 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 12 FDA reports)
ANAL ATRESIA ( 12 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
AORTIC DILATATION ( 12 FDA reports)
APPARENT DEATH ( 12 FDA reports)
AXILLARY MASS ( 12 FDA reports)
BARTHOLIN'S ABSCESS ( 12 FDA reports)
BARTHOLIN'S CYST ( 12 FDA reports)
BEREAVEMENT REACTION ( 12 FDA reports)
BILE DUCT OBSTRUCTION ( 12 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 12 FDA reports)
BLADDER DISCOMFORT ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 12 FDA reports)
BONE SARCOMA ( 12 FDA reports)
BRADYARRHYTHMIA ( 12 FDA reports)
BRAIN SCAN ABNORMAL ( 12 FDA reports)
BRONCHITIS ACUTE ( 12 FDA reports)
CALCULUS BLADDER ( 12 FDA reports)
CARBUNCLE ( 12 FDA reports)
CATHETER SEPSIS ( 12 FDA reports)
CATHETER SITE HAEMORRHAGE ( 12 FDA reports)
CEREBELLAR ATROPHY ( 12 FDA reports)
CERVICAL CORD COMPRESSION ( 12 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 12 FDA reports)
CHEST INJURY ( 12 FDA reports)
COLON CANCER STAGE III ( 12 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 12 FDA reports)
COMPULSIVE SHOPPING ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 12 FDA reports)
DERMATITIS ALLERGIC ( 12 FDA reports)
DEVICE RELATED SEPSIS ( 12 FDA reports)
DIAPHRAGMATIC DISORDER ( 12 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 12 FDA reports)
DRUG DETOXIFICATION ( 12 FDA reports)
EMPTY SELLA SYNDROME ( 12 FDA reports)
EPIGASTRIC DISCOMFORT ( 12 FDA reports)
EXERCISE TOLERANCE DECREASED ( 12 FDA reports)
FEEDING TUBE COMPLICATION ( 12 FDA reports)
FRACTURED COCCYX ( 12 FDA reports)
FUNGAL SKIN INFECTION ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
GINGIVAL GRAFT ( 12 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 12 FDA reports)
HAND DEFORMITY ( 12 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HISTOPLASMOSIS ( 12 FDA reports)
HODGKIN'S DISEASE ( 12 FDA reports)
ILIUM FRACTURE ( 12 FDA reports)
IMMOBILE ( 12 FDA reports)
INAPPROPRIATE AFFECT ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
INFUSION SITE PAIN ( 12 FDA reports)
INJECTION SITE INFECTION ( 12 FDA reports)
INJECTION SITE ULCER ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
IUD MIGRATION ( 12 FDA reports)
JUGULAR VEIN DISTENSION ( 12 FDA reports)
LABORATORY TEST INTERFERENCE ( 12 FDA reports)
LARGE INTESTINE PERFORATION ( 12 FDA reports)
LIMB MALFORMATION ( 12 FDA reports)
LUNG LOBECTOMY ( 12 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 12 FDA reports)
METASTASES TO NECK ( 12 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 12 FDA reports)
MITRAL VALVE HYPOPLASIA ( 12 FDA reports)
MULTIPLE ALLERGIES ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
OPEN ANGLE GLAUCOMA ( 12 FDA reports)
ORAL SOFT TISSUE DISORDER ( 12 FDA reports)
PELVIC MASS ( 12 FDA reports)
PLACENTA PRAEVIA ( 12 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
PRESSURE OF SPEECH ( 12 FDA reports)
PTERYGIUM ( 12 FDA reports)
PULMONARY HILUM MASS ( 12 FDA reports)
PUPILS UNEQUAL ( 12 FDA reports)
RAYNAUD'S PHENOMENON ( 12 FDA reports)
REACTIVE PSYCHOSIS ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
SIALOADENITIS ( 12 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 12 FDA reports)
SINUS ARRHYTHMIA ( 12 FDA reports)
SINUS RHYTHM ( 12 FDA reports)
SKIN PAPILLOMA ( 12 FDA reports)
SKIN TURGOR DECREASED ( 12 FDA reports)
SPINAL CORPECTOMY ( 12 FDA reports)
TENDON PAIN ( 12 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 12 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 12 FDA reports)
TOOTH DISCOLOURATION ( 12 FDA reports)
TOXIC ENCEPHALOPATHY ( 12 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
RENAL COLIC ( 11 FDA reports)
RESIDUAL URINE VOLUME ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RESPIRATORY ACIDOSIS ( 11 FDA reports)
RIB DEFORMITY ( 11 FDA reports)
SENSORY NEUROPATHY HEREDITARY ( 11 FDA reports)
SKIN NEOPLASM EXCISION ( 11 FDA reports)
SMALL FOR DATES BABY ( 11 FDA reports)
SMALL INTESTINAL PERFORATION ( 11 FDA reports)
SOMNOLENCE NEONATAL ( 11 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 11 FDA reports)
STATUS ASTHMATICUS ( 11 FDA reports)
SUBMANDIBULAR MASS ( 11 FDA reports)
SUNBURN ( 11 FDA reports)
THEFT ( 11 FDA reports)
THROMBOCYTHAEMIA ( 11 FDA reports)
TUMOUR MARKER INCREASED ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 11 FDA reports)
URINE FLOW DECREASED ( 11 FDA reports)
VASCULAR DEMENTIA ( 11 FDA reports)
VASCULAR GRAFT ( 11 FDA reports)
VASCULAR OCCLUSION ( 11 FDA reports)
VEIN DISORDER ( 11 FDA reports)
VENTRICULAR ARRHYTHMIA ( 11 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 11 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 11 FDA reports)
ADVERSE REACTION ( 11 FDA reports)
ALCOHOL INTERACTION ( 11 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 11 FDA reports)
ANTISOCIAL BEHAVIOUR ( 11 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 11 FDA reports)
ATRIAL TACHYCARDIA ( 11 FDA reports)
AUTOIMMUNE HEPATITIS ( 11 FDA reports)
BLADDER PAIN ( 11 FDA reports)
BLADDER SPASM ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 11 FDA reports)
BRAIN OPERATION ( 11 FDA reports)
BREAST ABSCESS ( 11 FDA reports)
BREAST LUMP REMOVAL ( 11 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 11 FDA reports)
BURNS SECOND DEGREE ( 11 FDA reports)
CARDIAC OPERATION ( 11 FDA reports)
CAROTID ARTERY ANEURYSM ( 11 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 11 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 11 FDA reports)
CLEFT LIP ( 11 FDA reports)
COLOSTOMY ( 11 FDA reports)
CUSHING'S SYNDROME ( 11 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 11 FDA reports)
DEPRESSIVE SYMPTOM ( 11 FDA reports)
DEVICE DISLOCATION ( 11 FDA reports)
DISORDER OF ORBIT ( 11 FDA reports)
DIURETIC THERAPY ( 11 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 11 FDA reports)
EJACULATION DELAYED ( 11 FDA reports)
EJACULATION DISORDER ( 11 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 11 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 11 FDA reports)
ENTHESOPATHY ( 11 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 11 FDA reports)
FOREARM FRACTURE ( 11 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 11 FDA reports)
HAEMORRHAGIC DIATHESIS ( 11 FDA reports)
HAIR GROWTH ABNORMAL ( 11 FDA reports)
HEAD BANGING ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYPOGLYCAEMIC COMA ( 11 FDA reports)
HYPOMENORRHOEA ( 11 FDA reports)
ILEITIS ( 11 FDA reports)
IMPAIRED SELF-CARE ( 11 FDA reports)
INCISION SITE COMPLICATION ( 11 FDA reports)
INCISION SITE PAIN ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 11 FDA reports)
INTRACRANIAL HYPOTENSION ( 11 FDA reports)
LEG AMPUTATION ( 11 FDA reports)
LIPIDS INCREASED ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 11 FDA reports)
LUNG HYPERINFLATION ( 11 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 11 FDA reports)
MENINGITIS VIRAL ( 11 FDA reports)
MOUTH INJURY ( 11 FDA reports)
OBSTRUCTION GASTRIC ( 11 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 11 FDA reports)
PELVIC VENOUS THROMBOSIS ( 11 FDA reports)
PHYSIOTHERAPY ( 11 FDA reports)
PLEURAL CALCIFICATION ( 11 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 11 FDA reports)
POIKILOCYTOSIS ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 11 FDA reports)
PREMATURE MENOPAUSE ( 11 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 11 FDA reports)
PREMENSTRUAL SYNDROME ( 11 FDA reports)
PROSTATOMEGALY ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
PULSE ABNORMAL ( 11 FDA reports)
QRS AXIS ABNORMAL ( 11 FDA reports)
ACUTE PULMONARY OEDEMA ( 10 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 10 FDA reports)
ALCOHOLIC LIVER DISEASE ( 10 FDA reports)
ALCOHOLIC PANCREATITIS ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANGIOMYOLIPOMA ( 10 FDA reports)
ANOGENITAL WARTS ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 10 FDA reports)
BICUSPID AORTIC VALVE ( 10 FDA reports)
BLADDER CYST ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 10 FDA reports)
BLOOD FOLATE INCREASED ( 10 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 10 FDA reports)
BONE FISTULA ( 10 FDA reports)
BREAST FIBROSIS ( 10 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
CHEMOTHERAPY ( 10 FDA reports)
COLECTOMY ( 10 FDA reports)
CONGENITAL LARGE INTESTINAL ATRESIA ( 10 FDA reports)
DEFORMITY THORAX ( 10 FDA reports)
DENTAL TREATMENT ( 10 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 10 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 10 FDA reports)
EMBOLISM ARTERIAL ( 10 FDA reports)
ENTEROBACTER INFECTION ( 10 FDA reports)
EXCESSIVE EYE BLINKING ( 10 FDA reports)
EXTRADURAL HAEMATOMA ( 10 FDA reports)
EYELID DISORDER ( 10 FDA reports)
EYELID RETRACTION ( 10 FDA reports)
FOETAL DISORDER ( 10 FDA reports)
FOETAL HEART RATE ABNORMAL ( 10 FDA reports)
FOREIGN BODY ASPIRATION ( 10 FDA reports)
FOREIGN BODY TRAUMA ( 10 FDA reports)
GANGLION ( 10 FDA reports)
GASTRIC POLYPS ( 10 FDA reports)
GRANDIOSITY ( 10 FDA reports)
HAEMANGIOMA OF LIVER ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HAEMORRHOID OPERATION ( 10 FDA reports)
HEART VALVE INSUFFICIENCY ( 10 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 10 FDA reports)
IATROGENIC INJURY ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
IMPLANT SITE INFLAMMATION ( 10 FDA reports)
IMPLANT SITE PAIN ( 10 FDA reports)
INGROWN HAIR ( 10 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 10 FDA reports)
JOINT SURGERY ( 10 FDA reports)
KIDNEY ENLARGEMENT ( 10 FDA reports)
LEUKOENCEPHALOPATHY ( 10 FDA reports)
LUNG ADENOCARCINOMA ( 10 FDA reports)
LYMPHADENECTOMY ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
LYMPHOCYTOSIS ( 10 FDA reports)
MACROPHAGES INCREASED ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 10 FDA reports)
MENSTRUATION DELAYED ( 10 FDA reports)
METATARSALGIA ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
MIDDLE EAR EFFUSION ( 10 FDA reports)
NASAL OEDEMA ( 10 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 10 FDA reports)
OCCIPITAL NEURALGIA ( 10 FDA reports)
OCULAR HYPERTENSION ( 10 FDA reports)
OESOPHAGITIS ULCERATIVE ( 10 FDA reports)
OLIGOHYDRAMNIOS ( 10 FDA reports)
ONYCHOMADESIS ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
ORGANISING PNEUMONIA ( 10 FDA reports)
ORTHOSTATIC HYPERTENSION ( 10 FDA reports)
PARAPROTEINAEMIA ( 10 FDA reports)
PLACENTAL DISORDER ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 10 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 10 FDA reports)
PROCEDURAL HYPOTENSION ( 10 FDA reports)
PROLAPSE REPAIR ( 10 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 10 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 10 FDA reports)
SALPINGO-OOPHORECTOMY ( 10 FDA reports)
SKIN ATROPHY ( 10 FDA reports)
STENOTROPHOMONAS INFECTION ( 10 FDA reports)
STILLBIRTH ( 10 FDA reports)
TENOSYNOVITIS ( 10 FDA reports)
TERATOMA ( 10 FDA reports)
TRACHEOSTOMY ( 10 FDA reports)
TURNER'S SYNDROME ( 10 FDA reports)
URINARY TRACT DISORDER ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
VERTEBROPLASTY ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
VULVOVAGINAL PAIN ( 10 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
RESUSCITATION ( 9 FDA reports)
RETINAL VEIN OCCLUSION ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
SALIVARY GLAND CALCULUS ( 9 FDA reports)
SCAN ABNORMAL ( 9 FDA reports)
SCAPULA FRACTURE ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SEPSIS SYNDROME ( 9 FDA reports)
SERRATIA INFECTION ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKULL FRACTURE ( 9 FDA reports)
SMOKER ( 9 FDA reports)
SOFT TISSUE INFECTION ( 9 FDA reports)
SOMATOFORM DISORDER ( 9 FDA reports)
SPINAL DEFORMITY ( 9 FDA reports)
SPONDYLITIC MYELOPATHY ( 9 FDA reports)
SPUTUM CULTURE POSITIVE ( 9 FDA reports)
STEATORRHOEA ( 9 FDA reports)
STRESS INCONTINENCE ( 9 FDA reports)
STRIDOR ( 9 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 9 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
TERMINAL STATE ( 9 FDA reports)
TESTICULAR PAIN ( 9 FDA reports)
TONGUE DRY ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
UTERINE CANCER ( 9 FDA reports)
VAGINAL MYCOSIS ( 9 FDA reports)
VARICOCELE ( 9 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 9 FDA reports)
VENOUS OCCLUSION ( 9 FDA reports)
VESICOURETERIC REFLUX ( 9 FDA reports)
VOMITING PROJECTILE ( 9 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 9 FDA reports)
WEGENER'S GRANULOMATOSIS ( 9 FDA reports)
WISDOM TEETH REMOVAL ( 9 FDA reports)
ADRENAL MASS ( 9 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
ANORECTAL DISORDER ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 9 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
AUTOIMMUNE DISORDER ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BLADDER DYSFUNCTION ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 9 FDA reports)
BONE FORMATION INCREASED ( 9 FDA reports)
BONE TRIMMING ( 9 FDA reports)
BRAIN DAMAGE ( 9 FDA reports)
BREECH PRESENTATION ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
BRONCHIOLITIS ( 9 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 9 FDA reports)
CARBON DIOXIDE INCREASED ( 9 FDA reports)
CARDIAC FAILURE CHRONIC ( 9 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 9 FDA reports)
CARDIOPULMONARY FAILURE ( 9 FDA reports)
CEREBELLAR SYNDROME ( 9 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 9 FDA reports)
CERVICITIS ( 9 FDA reports)
CHANGE OF BOWEL HABIT ( 9 FDA reports)
CHEST TUBE INSERTION ( 9 FDA reports)
CHOLECYSTITIS INFECTIVE ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CHONDROPLASTY ( 9 FDA reports)
CHOREOATHETOSIS ( 9 FDA reports)
CLAUSTROPHOBIA ( 9 FDA reports)
CLEFT LIP AND PALATE ( 9 FDA reports)
CONGENITAL HAIR DISORDER ( 9 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 9 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 9 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 9 FDA reports)
DEATH OF RELATIVE ( 9 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 9 FDA reports)
DERMOID CYST ( 9 FDA reports)
DRUG EFFECT INCREASED ( 9 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 9 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 9 FDA reports)
DYSPHASIA ( 9 FDA reports)
EAR TUBE INSERTION ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 9 FDA reports)
ELEVATED MOOD ( 9 FDA reports)
EMBOLISM VENOUS ( 9 FDA reports)
ENEMA ADMINISTRATION ( 9 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
EYE OEDEMA ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FISTULA REPAIR ( 9 FDA reports)
FLIGHT OF IDEAS ( 9 FDA reports)
FOETAL HEART RATE DECREASED ( 9 FDA reports)
FOOD ALLERGY ( 9 FDA reports)
FOOD POISONING ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
FRACTURE DISPLACEMENT ( 9 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 9 FDA reports)
GINGIVAL ABSCESS ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HAEMATOMA INFECTION ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 9 FDA reports)
HEREDITARY ANGIOEDEMA ( 9 FDA reports)
HYPERBILIRUBINAEMIA ( 9 FDA reports)
HYPERCHLORHYDRIA ( 9 FDA reports)
HYPERMETROPIA ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
HYPERPLASIA ( 9 FDA reports)
INDUCED LABOUR ( 9 FDA reports)
INJECTION SITE NECROSIS ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
LACTIC ACIDOSIS ( 9 FDA reports)
LAZINESS ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
LIP BLISTER ( 9 FDA reports)
LIP DISORDER ( 9 FDA reports)
LIPID METABOLISM DISORDER ( 9 FDA reports)
MALIGNANT HYPERTENSION ( 9 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 9 FDA reports)
MEDIASTINAL DISORDER ( 9 FDA reports)
MENIERE'S DISEASE ( 9 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 9 FDA reports)
MORBID THOUGHTS ( 9 FDA reports)
MUCOUS MEMBRANE DISORDER ( 9 FDA reports)
MULTI-ORGAN DISORDER ( 9 FDA reports)
MYOCARDITIS ( 9 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 9 FDA reports)
MYRINGITIS ( 9 FDA reports)
NAIL DISCOLOURATION ( 9 FDA reports)
NEONATAL TACHYPNOEA ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 9 FDA reports)
OLIGOMENORRHOEA ( 9 FDA reports)
OPTIC ATROPHY ( 9 FDA reports)
ORAL TORUS ( 9 FDA reports)
ORBITAL OEDEMA ( 9 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 9 FDA reports)
PERINEAL CYST ( 9 FDA reports)
PERIODONTAL OPERATION ( 9 FDA reports)
PERITONEAL ADHESIONS ( 9 FDA reports)
PERNICIOUS ANAEMIA ( 9 FDA reports)
PERSECUTORY DELUSION ( 9 FDA reports)
PICKWICKIAN SYNDROME ( 9 FDA reports)
PITUITARY TUMOUR ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
PO2 INCREASED ( 9 FDA reports)
POOR PERIPHERAL CIRCULATION ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
POST CONCUSSION SYNDROME ( 9 FDA reports)
PREMATURE DELIVERY ( 9 FDA reports)
PRESBYACUSIS ( 9 FDA reports)
PSEUDOCYST ( 9 FDA reports)
PTERYGIUM COLLI ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ABORTION THREATENED ( 8 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACTINOMYCES TEST POSITIVE ( 8 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 8 FDA reports)
ALLODYNIA ( 8 FDA reports)
AMPHETAMINES ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 8 FDA reports)
ANURIA ( 8 FDA reports)
APPLICATION SITE BURN ( 8 FDA reports)
AURA ( 8 FDA reports)
AUTOMATISM ( 8 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 8 FDA reports)
BARBITURATES ( 8 FDA reports)
BENIGN VASCULAR NEOPLASM ( 8 FDA reports)
BIFASCICULAR BLOCK ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD CORTISOL DECREASED ( 8 FDA reports)
BLOOD CREATININE DECREASED ( 8 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 8 FDA reports)
BRACHIAL PLEXOPATHY ( 8 FDA reports)
BRADYCARDIA NEONATAL ( 8 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 8 FDA reports)
BREAST DISORDER ( 8 FDA reports)
BREAST DISORDER FEMALE ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
BULIMIA NERVOSA ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
CALCIUM DEFICIENCY ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 8 FDA reports)
CLAVICLE FRACTURE ( 8 FDA reports)
COGWHEEL RIGIDITY ( 8 FDA reports)
COLON CANCER STAGE I ( 8 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 8 FDA reports)
COMPLICATION OF PREGNANCY ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CONDUCT DISORDER ( 8 FDA reports)
CORNEAL OEDEMA ( 8 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
CSF TEST ABNORMAL ( 8 FDA reports)
CYTOGENETIC ABNORMALITY ( 8 FDA reports)
DEATH OF FRIEND ( 8 FDA reports)
DEREALISATION ( 8 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 8 FDA reports)
DRUG INTERACTION INHIBITION ( 8 FDA reports)
DRUG TOLERANCE INCREASED ( 8 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 8 FDA reports)
ENAMEL ANOMALY ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENDOSCOPY ( 8 FDA reports)
ENTEROCOLITIS ( 8 FDA reports)
FAT INTOLERANCE ( 8 FDA reports)
FEEDING DISORDER ( 8 FDA reports)
GALLBLADDER POLYP ( 8 FDA reports)
GASTRECTOMY ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTROINTESTINAL ULCER ( 8 FDA reports)
GASTROSTOMY TUBE INSERTION ( 8 FDA reports)
GLIOBLASTOMA MULTIFORME ( 8 FDA reports)
GUILLAIN-BARRE SYNDROME ( 8 FDA reports)
HAEMOCHROMATOSIS ( 8 FDA reports)
HEPATOSPLENOMEGALY ( 8 FDA reports)
HICCUPS ( 8 FDA reports)
HIGH FREQUENCY ABLATION ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
HYPERPARATHYROIDISM ( 8 FDA reports)
HYPERSEXUALITY ( 8 FDA reports)
HYPERTRANSAMINASAEMIA ( 8 FDA reports)
HYPOCHLORAEMIA ( 8 FDA reports)
HYPOCHROMIC ANAEMIA ( 8 FDA reports)
HYPOPROTEINAEMIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
HYPOTONIA NEONATAL ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INJECTION SITE CELLULITIS ( 8 FDA reports)
INJECTION SITE OEDEMA ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
KNEE DEFORMITY ( 8 FDA reports)
LIMB ASYMMETRY ( 8 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 8 FDA reports)
LYMPHATIC DISORDER ( 8 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 8 FDA reports)
METASTASES TO PLEURA ( 8 FDA reports)
MOTION SICKNESS ( 8 FDA reports)
MURDER ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NAIL OPERATION ( 8 FDA reports)
NO ADVERSE EFFECT ( 8 FDA reports)
NODULE ON EXTREMITY ( 8 FDA reports)
OESOPHAGEAL ACHALASIA ( 8 FDA reports)
OROPHARYNGEAL SWELLING ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
OVARIAN NEOPLASM ( 8 FDA reports)
PANCREATITIS NECROTISING ( 8 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 8 FDA reports)
PARESIS ( 8 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 8 FDA reports)
PERIODONTAL INFECTION ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PHARYNGEAL INFLAMMATION ( 8 FDA reports)
PHLEBOLITH ( 8 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 8 FDA reports)
POLYMENORRHOEA ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
POLYPECTOMY ( 8 FDA reports)
POLYSUBSTANCE ABUSE ( 8 FDA reports)
POSTOPERATIVE INFECTION ( 8 FDA reports)
POSTPARTUM HAEMORRHAGE ( 8 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 8 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 8 FDA reports)
PROSTHESIS IMPLANTATION ( 8 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 8 FDA reports)
PSYCHOSOMATIC DISEASE ( 8 FDA reports)
PULMONARY VALVE STENOSIS ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
RADICAL MASTECTOMY ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
REGRESSIVE BEHAVIOUR ( 8 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 8 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 8 FDA reports)
SECRETION DISCHARGE ( 8 FDA reports)
SERUM SEROTONIN INCREASED ( 8 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 8 FDA reports)
SKIN CHAPPED ( 8 FDA reports)
SKIN INJURY ( 8 FDA reports)
SKIN ODOUR ABNORMAL ( 8 FDA reports)
SLEEP-RELATED EATING DISORDER ( 8 FDA reports)
SPLENIC GRANULOMA ( 8 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 8 FDA reports)
SUFFOCATION FEELING ( 8 FDA reports)
THALAMIC INFARCTION ( 8 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 8 FDA reports)
TONGUE BLISTERING ( 8 FDA reports)
TONGUE PARALYSIS ( 8 FDA reports)
TOOTH IMPACTED ( 8 FDA reports)
TRICHOTILLOMANIA ( 8 FDA reports)
TRISOMY 21 ( 8 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
URINE ABNORMALITY ( 8 FDA reports)
VOCAL CORD DISORDER ( 8 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 8 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 7 FDA reports)
RELATIONSHIP BREAKDOWN ( 7 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 7 FDA reports)
RENAL TRANSPLANT ( 7 FDA reports)
RESIDUAL URINE ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SHOULDER OPERATION ( 7 FDA reports)
SKIN CANDIDA ( 7 FDA reports)
SKIN FISSURES ( 7 FDA reports)
SMEAR CERVIX ABNORMAL ( 7 FDA reports)
SPINAL COLUMN INJURY ( 7 FDA reports)
SPONDYLITIS ( 7 FDA reports)
TACHYARRHYTHMIA ( 7 FDA reports)
THERAPY REGIMEN CHANGED ( 7 FDA reports)
THYROID MASS ( 7 FDA reports)
TINEA VERSICOLOUR ( 7 FDA reports)
TRAUMATIC FRACTURE ( 7 FDA reports)
TROPONIN I INCREASED ( 7 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 7 FDA reports)
TUMOUR HAEMORRHAGE ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
URINE COLOUR ABNORMAL ( 7 FDA reports)
VAGINAL CANDIDIASIS ( 7 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VICTIM OF CRIME ( 7 FDA reports)
VITREOUS DETACHMENT ( 7 FDA reports)
WEIGHT GAIN POOR ( 7 FDA reports)
WHIPLASH INJURY ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 7 FDA reports)
ALOPECIA SCARRING ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANION GAP INCREASED ( 7 FDA reports)
APPLICATION SITE ULCER ( 7 FDA reports)
ASPIRATION BREAST ( 7 FDA reports)
ATROPHY ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BILIARY TRACT DISORDER ( 7 FDA reports)
BIOPSY BREAST ABNORMAL ( 7 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 7 FDA reports)
BLOOD AMYLASE DECREASED ( 7 FDA reports)
BLOOD PROLACTIN INCREASED ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 7 FDA reports)
BRAIN STEM INFARCTION ( 7 FDA reports)
BREAST CELLULITIS ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CLONUS ( 7 FDA reports)
CONGENITAL AORTIC STENOSIS ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CULTURE WOUND POSITIVE ( 7 FDA reports)
CUSHINGOID ( 7 FDA reports)
DEAFNESS BILATERAL ( 7 FDA reports)
DEATH NEONATAL ( 7 FDA reports)
DEMENTIA WITH LEWY BODIES ( 7 FDA reports)
DETOXIFICATION ( 7 FDA reports)
DEVICE INEFFECTIVE ( 7 FDA reports)
DIABETES INSIPIDUS ( 7 FDA reports)
DIET REFUSAL ( 7 FDA reports)
DISLOCATION OF VERTEBRA ( 7 FDA reports)
DIVERTICULAR PERFORATION ( 7 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 7 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
DYSMORPHISM ( 7 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ENDARTERECTOMY ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
FLASHBACK ( 7 FDA reports)
FOETAL MOVEMENTS DECREASED ( 7 FDA reports)
FOOD AVERSION ( 7 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 7 FDA reports)
GALLBLADDER ENLARGEMENT ( 7 FDA reports)
GLUCOSE URINE PRESENT ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
HEPATIC ADENOMA ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HYDROCHOLECYSTIS ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 7 FDA reports)
ILIAC ARTERY STENOSIS ( 7 FDA reports)
ILLUSION ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
JOINT CREPITATION ( 7 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 7 FDA reports)
KELOID SCAR ( 7 FDA reports)
LARGE FOR DATES BABY ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LIPIDS ABNORMAL ( 7 FDA reports)
LIVE BIRTH ( 7 FDA reports)
LUMBAR HERNIA ( 7 FDA reports)
LUNG CANCER METASTATIC ( 7 FDA reports)
LYMPH NODE CANCER METASTATIC ( 7 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MARITAL PROBLEM ( 7 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 7 FDA reports)
MIGRAINE WITH AURA ( 7 FDA reports)
MOANING ( 7 FDA reports)
MYASTHENIA GRAVIS ( 7 FDA reports)
NEONATAL HYPOTENSION ( 7 FDA reports)
NEUTROPENIC INFECTION ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
NOSOCOMIAL INFECTION ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
ORTHOSTATIC INTOLERANCE ( 7 FDA reports)
OSTECTOMY ( 7 FDA reports)
OSTEITIS DEFORMANS ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PANCREATIC PSEUDOCYST ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PERITONITIS BACTERIAL ( 7 FDA reports)
PLATELET COUNT ABNORMAL ( 7 FDA reports)
PLATELET DISORDER ( 7 FDA reports)
PNEUMOPERITONEUM ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POLYP COLORECTAL ( 7 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 7 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 7 FDA reports)
PRECANCEROUS CELLS PRESENT ( 7 FDA reports)
PROLACTINOMA ( 7 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
PSYCHOMOTOR RETARDATION ( 7 FDA reports)
PULMONARY HYPOPLASIA ( 7 FDA reports)
PULMONARY VALVE DISEASE ( 7 FDA reports)
PYELONEPHRITIS ACUTE ( 7 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ADNEXA UTERI MASS ( 6 FDA reports)
ADRENAL ADENOMA ( 6 FDA reports)
ALCOHOLIC ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
APPLICATION SITE EXCORIATION ( 6 FDA reports)
ARTERIAL STENOSIS ( 6 FDA reports)
ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
ATHEROSCLEROSIS ( 6 FDA reports)
AXILLARY VEIN THROMBOSIS ( 6 FDA reports)
B-CELL LYMPHOMA ( 6 FDA reports)
BACTERIA STOOL IDENTIFIED ( 6 FDA reports)
BENCE JONES PROTEINURIA ( 6 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 6 FDA reports)
BENIGN NEOPLASM OF SKIN ( 6 FDA reports)
BIOPSY ENDOMETRIUM ( 6 FDA reports)
BIOPSY SKIN ( 6 FDA reports)
BLADDER INJURY ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BLOOD GASES ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 6 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 6 FDA reports)
BONE INFARCTION ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BRAIN MIDLINE SHIFT ( 6 FDA reports)
BREAST HAEMATOMA ( 6 FDA reports)
BREAST INFECTION ( 6 FDA reports)
BRONCHIAL WALL THICKENING ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CAUSTIC INJURY ( 6 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COCCIDIOIDOMYCOSIS ( 6 FDA reports)
COLON INJURY ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
CONDUCTIVE DEAFNESS ( 6 FDA reports)
CONFABULATION ( 6 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 6 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 6 FDA reports)
COR PULMONALE ( 6 FDA reports)
CRANIOCEREBRAL INJURY ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
DIABETIC EYE DISEASE ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
ECTOPIC PREGNANCY ( 6 FDA reports)
ELECTROLYTE DEPLETION ( 6 FDA reports)
ENCEPHALITIS VIRAL ( 6 FDA reports)
ENCHONDROMA ( 6 FDA reports)
ENDOCRINE DISORDER ( 6 FDA reports)
EXERCISE LACK OF ( 6 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 6 FDA reports)
EXPOSURE TO TOXIC AGENT ( 6 FDA reports)
FAT TISSUE INCREASED ( 6 FDA reports)
FORCEPS DELIVERY ( 6 FDA reports)
GAIT SPASTIC ( 6 FDA reports)
GALLOP RHYTHM PRESENT ( 6 FDA reports)
GENERAL SYMPTOM ( 6 FDA reports)
GENITAL BURNING SENSATION ( 6 FDA reports)
GENITAL RASH ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGE URINARY TRACT ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HOARSENESS ( 6 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 6 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 6 FDA reports)
HYPERVIGILANCE ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
IMMUNODEFICIENCY ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
IMPLANT SITE DISCHARGE ( 6 FDA reports)
INCREASED INSULIN REQUIREMENT ( 6 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INJECTION SITE INFLAMMATION ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTESTINAL RESECTION ( 6 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 6 FDA reports)
JOINT HYPEREXTENSION ( 6 FDA reports)
JOINT INJECTION ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
LICE INFESTATION ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 6 FDA reports)
LUNG OPERATION ( 6 FDA reports)
MADAROSIS ( 6 FDA reports)
MALE ORGASMIC DISORDER ( 6 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 6 FDA reports)
MASTOIDITIS ( 6 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 6 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 6 FDA reports)
MEDICAL DIET ( 6 FDA reports)
METASTASES TO MUSCLE ( 6 FDA reports)
MICTURITION FREQUENCY DECREASED ( 6 FDA reports)
MUSCLE FATIGUE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE HAEMORRHAGE ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
MYELOMA RECURRENCE ( 6 FDA reports)
MYRINGOTOMY ( 6 FDA reports)
NASAL NEOPLASM ( 6 FDA reports)
NASAL OBSTRUCTION ( 6 FDA reports)
NASAL POLYPS ( 6 FDA reports)
NEONATAL RESPIRATORY ARREST ( 6 FDA reports)
NEOPLASM OF APPENDIX ( 6 FDA reports)
NERVE ROOT COMPRESSION ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
OESTRADIOL DECREASED ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
OROPHARYNGEAL BLISTERING ( 6 FDA reports)
OSTEOMYELITIS ACUTE ( 6 FDA reports)
OVARIAN CYST RUPTURED ( 6 FDA reports)
PANCREATIC NECROSIS ( 6 FDA reports)
PARADOXICAL DRUG REACTION ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 6 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 6 FDA reports)
PERSEVERATION ( 6 FDA reports)
PHIMOSIS ( 6 FDA reports)
PHLEBITIS SUPERFICIAL ( 6 FDA reports)
PLANTAR ERYTHEMA ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
POOR SUCKING REFLEX ( 6 FDA reports)
POSTICTAL HEADACHE ( 6 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 6 FDA reports)
PULMONARY CAVITATION ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
PYOTHORAX ( 6 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 6 FDA reports)
REBOUND EFFECT ( 6 FDA reports)
RECTAL DISCHARGE ( 6 FDA reports)
RESPIRATORY ALKALOSIS ( 6 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 6 FDA reports)
RHYTHM IDIOVENTRICULAR ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 6 FDA reports)
SCLERAL DISORDER ( 6 FDA reports)
SEXUAL ASSAULT VICTIM ( 6 FDA reports)
SHOCK HAEMORRHAGIC ( 6 FDA reports)
SKIN DEPIGMENTATION ( 6 FDA reports)
SKIN OEDEMA ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
SPUTUM PURULENT ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
STILL'S DISEASE ADULT ONSET ( 6 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 6 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
SUTURE REMOVAL ( 6 FDA reports)
SWOLLEN TEAR DUCT ( 6 FDA reports)
THYROXINE DECREASED ( 6 FDA reports)
TOE OPERATION ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TONSILLAR DISORDER ( 6 FDA reports)
TOOTH INJURY ( 6 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 6 FDA reports)
TRANSPLANT REJECTION ( 6 FDA reports)
TRICHORRHEXIS ( 6 FDA reports)
ULCERATIVE KERATITIS ( 6 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
URETERIC OBSTRUCTION ( 6 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 6 FDA reports)
UTERINE SPASM ( 6 FDA reports)
VENOUS INJURY ( 6 FDA reports)
VOLUME BLOOD DECREASED ( 6 FDA reports)
VULVAL CANCER ( 6 FDA reports)
RECTAL TENESMUS ( 5 FDA reports)
RECTOCELE REPAIR ( 5 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL CANCER ( 5 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 5 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 5 FDA reports)
RETINAL ARTERY OCCLUSION ( 5 FDA reports)
RETINAL VASCULAR DISORDER ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SEPTIC EMBOLUS ( 5 FDA reports)
SEROSITIS ( 5 FDA reports)
SHOPLIFTING ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 5 FDA reports)
SPINAL PAIN ( 5 FDA reports)
SPINE MALFORMATION ( 5 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
SUBCUTANEOUS NODULE ( 5 FDA reports)
THROAT CANCER ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
THYROID CYST ( 5 FDA reports)
TONGUE HAEMORRHAGE ( 5 FDA reports)
TOOTH EROSION ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TRISOMY 18 ( 5 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 5 FDA reports)
URETERAL STENT INSERTION ( 5 FDA reports)
URETHRAL DILATATION ( 5 FDA reports)
URETHRAL FISTULA ( 5 FDA reports)
URETHRAL OBSTRUCTION ( 5 FDA reports)
URINARY TRACT OPERATION ( 5 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
UTERINE CYST ( 5 FDA reports)
UTERINE DILATION AND CURETTAGE ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VAGINAL FISTULA ( 5 FDA reports)
VAGINAL NEOPLASM ( 5 FDA reports)
VAGINAL ODOUR ( 5 FDA reports)
VASCULAR DISSECTION ( 5 FDA reports)
VESTIBULAR DISORDER ( 5 FDA reports)
VITREOUS DISORDER ( 5 FDA reports)
VOCAL CORD INFLAMMATION ( 5 FDA reports)
VOCAL CORD POLYP ( 5 FDA reports)
VULVA CYST ( 5 FDA reports)
VULVAL OEDEMA ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
ABDOMINAL OPERATION ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ADDISON'S DISEASE ( 5 FDA reports)
AGITATION NEONATAL ( 5 FDA reports)
AMYLOIDOSIS ( 5 FDA reports)
ANKYLOSING SPONDYLITIS ( 5 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 5 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 5 FDA reports)
APALLIC SYNDROME ( 5 FDA reports)
APHERESIS ( 5 FDA reports)
APPETITE DISORDER ( 5 FDA reports)
APPLICATION SITE URTICARIA ( 5 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 5 FDA reports)
ARTHROSCOPIC SURGERY ( 5 FDA reports)
ASTIGMATISM ( 5 FDA reports)
AUTISM ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BENIGN HEPATIC NEOPLASM ( 5 FDA reports)
BLADDER CANCER STAGE III ( 5 FDA reports)
BLADDER HYPERTROPHY ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY INCREASED ( 5 FDA reports)
BONE MARROW NECROSIS ( 5 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 5 FDA reports)
BRAIN CANCER METASTATIC ( 5 FDA reports)
BRONCHIAL SECRETION RETENTION ( 5 FDA reports)
BRONCHOPULMONARY DISEASE ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CARCINOID SYNDROME ( 5 FDA reports)
CARDIAC AMYLOIDOSIS ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CATHETER SITE PAIN ( 5 FDA reports)
CATHETER SITE SWELLING ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CEREBRAL CYST ( 5 FDA reports)
CHRONIC HEPATITIS ( 5 FDA reports)
COLON POLYPECTOMY ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 5 FDA reports)
CONGENITAL FOOT MALFORMATION ( 5 FDA reports)
CONGENITAL NOSE MALFORMATION ( 5 FDA reports)
CORNEAL EROSION ( 5 FDA reports)
CSF PROTEIN INCREASED ( 5 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 5 FDA reports)
CYSTITIS NONINFECTIVE ( 5 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 5 FDA reports)
DEATH OF SIBLING ( 5 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 5 FDA reports)
DELUSIONAL PERCEPTION ( 5 FDA reports)
DENTAL IMPLANTATION ( 5 FDA reports)
DENTAL NECROSIS ( 5 FDA reports)
DEVICE EXPULSION ( 5 FDA reports)
DIABETIC ULCER ( 5 FDA reports)
DISINHIBITION ( 5 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DUODENAL POLYP ( 5 FDA reports)
DYSPNOEA AT REST ( 5 FDA reports)
ECZEMA INFECTED ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 5 FDA reports)
EXCITABILITY ( 5 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 5 FDA reports)
FIBROMA ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
GALLBLADDER CANCER ( 5 FDA reports)
GALLBLADDER OBSTRUCTION ( 5 FDA reports)
GENITAL HAEMORRHAGE ( 5 FDA reports)
GENITAL SWELLING ( 5 FDA reports)
GIARDIASIS ( 5 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 5 FDA reports)
GOUTY ARTHRITIS ( 5 FDA reports)
GRIEF REACTION ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMATOCRIT ABNORMAL ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEPATIC RUPTURE ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HOSPICE CARE ( 5 FDA reports)
HYPERAEMIA ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPERTENSION NEONATAL ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
IGA NEPHROPATHY ( 5 FDA reports)
INCLUSION BODY MYOSITIS ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INJECTION SITE ABSCESS ( 5 FDA reports)
INJECTION SITE PAPULE ( 5 FDA reports)
INJECTION SITE SCAR ( 5 FDA reports)
INJECTION SITE THROMBOSIS ( 5 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 5 FDA reports)
INTERVERTEBRAL DISC INJURY ( 5 FDA reports)
INTESTINAL MASS ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
JOB DISSATISFACTION ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LARYNGEAL WEB ( 5 FDA reports)
LEIOMYOMA ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 5 FDA reports)
LIMB OPERATION ( 5 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 5 FDA reports)
LIP EXFOLIATION ( 5 FDA reports)
LOWER EXTREMITY MASS ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
MAGNESIUM DEFICIENCY ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 5 FDA reports)
MAMMOGRAM ABNORMAL ( 5 FDA reports)
MANDIBULAR PROSTHESIS USER ( 5 FDA reports)
MASTOPTOSIS ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
MEDIAN NERVE INJURY ( 5 FDA reports)
MEDIASTINAL MASS ( 5 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 5 FDA reports)
MENOMETRORRHAGIA ( 5 FDA reports)
MICROCEPHALY ( 5 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCKLE-WELLS SYNDROME ( 5 FDA reports)
MUCOSAL DRYNESS ( 5 FDA reports)
MUTISM ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
NAIL HYPERTROPHY ( 5 FDA reports)
NASAL ULCER ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
NEUTROPENIC SEPSIS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
NORMAL NEWBORN ( 5 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 5 FDA reports)
OCULAR VASCULAR DISORDER ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
OESOPHAGEAL DILATATION ( 5 FDA reports)
OSTEOCHONDRITIS ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PALATAL OEDEMA ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 5 FDA reports)
PARANEOPLASTIC SYNDROME ( 5 FDA reports)
PARASOMNIA ( 5 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PELVIC DISCOMFORT ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PITUITARY TUMOUR BENIGN ( 5 FDA reports)
PNEUMOCEPHALUS ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
POST PROCEDURAL NAUSEA ( 5 FDA reports)
POST PROCEDURAL VOMITING ( 5 FDA reports)
POSTOPERATIVE FEVER ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PREMATURE EJACULATION ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROSTATE INFECTION ( 5 FDA reports)
PROSTHESIS USER ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PSYCHOTIC BEHAVIOUR ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
PULMONARY ARTERY STENOSIS ( 5 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABDOMINAL RIGIDITY ( 4 FDA reports)
ABNORMAL WEIGHT GAIN ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
ACTINIC ELASTOSIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE TONSILLITIS ( 4 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 4 FDA reports)
ALLERGIC COUGH ( 4 FDA reports)
AMAUROSIS FUGAX ( 4 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 4 FDA reports)
ANENCEPHALY ( 4 FDA reports)
ANIMAL SCRATCH ( 4 FDA reports)
ANTEROGRADE AMNESIA ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
APPENDIX DISORDER ( 4 FDA reports)
APPLICATION SITE DERMATITIS ( 4 FDA reports)
APPLICATION SITE SCAB ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ARTERIAL THROMBOSIS ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ARTHROPOD STING ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
AUTOMATIC BLADDER ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 4 FDA reports)
BLOOD CREATININE ABNORMAL ( 4 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 4 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE ( 4 FDA reports)
BLOOD URINE ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE MARROW OEDEMA ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST CYST DRAINAGE ( 4 FDA reports)
BREAST MICROCALCIFICATION ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 4 FDA reports)
CARDIAC VALVE SCLEROSIS ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CATARACT CORTICAL ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CATHETER SITE INFLAMMATION ( 4 FDA reports)
CATHETER SITE RASH ( 4 FDA reports)
CENTRAL LINE INFECTION ( 4 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 4 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 4 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHLAMYDIAL INFECTION ( 4 FDA reports)
CHOLANGITIS SCLEROSING ( 4 FDA reports)
CHORIOAMNIONITIS ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 4 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 4 FDA reports)
COLON CANCER RECURRENT ( 4 FDA reports)
COLORECTAL CANCER METASTATIC ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 4 FDA reports)
CONFUSION POSTOPERATIVE ( 4 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 4 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 4 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORNEAL DYSTROPHY ( 4 FDA reports)
CORONARY ARTERY DISSECTION ( 4 FDA reports)
CRANIAL NERVE DISORDER ( 4 FDA reports)
CRANIECTOMY ( 4 FDA reports)
CREATININE URINE DECREASED ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CRYPTORCHISM ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CUTIS LAXA ( 4 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DENTAL DISCOMFORT ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVICE ADHESION ISSUE ( 4 FDA reports)
DEVICE MISUSE ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DISSOCIATIVE FUGUE ( 4 FDA reports)
DROWNING ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRUG TOLERANCE DECREASED ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
EAR INFECTION FUNGAL ( 4 FDA reports)
EAR INJURY ( 4 FDA reports)
EAR OPERATION ( 4 FDA reports)
ENDOMETRIAL DISORDER ( 4 FDA reports)
ENLARGED CLITORIS ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
ESCHERICHIA BACTERAEMIA ( 4 FDA reports)
EXCESSIVE MASTURBATION ( 4 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 4 FDA reports)
EXTERNAL EAR CELLULITIS ( 4 FDA reports)
EXTRAVASATION ( 4 FDA reports)
EYE INFLAMMATION ( 4 FDA reports)
FACIAL DYSMORPHISM ( 4 FDA reports)
FACIAL WASTING ( 4 FDA reports)
FACTITIOUS DISORDER ( 4 FDA reports)
FALLOPIAN TUBE DISORDER ( 4 FDA reports)
FEAR OF DISEASE ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FOLATE DEFICIENCY ( 4 FDA reports)
FOOD INTERACTION ( 4 FDA reports)
FRACTURE MALUNION ( 4 FDA reports)
GASTRIC VARICES ( 4 FDA reports)
GASTROENTERITIS BACTERIAL ( 4 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GASTROINTESTINAL SURGERY ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GASTROSCHISIS ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER INFECTION ( 4 FDA reports)
HEMIANOPIA HETERONYMOUS ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEMICEPHALALGIA ( 4 FDA reports)
HEPATIC ARTERY ANEURYSM ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HERPES DERMATITIS ( 4 FDA reports)
HERPES PHARYNGITIS ( 4 FDA reports)
HORDEOLUM ( 4 FDA reports)
HYDROURETER ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERTENSIVE EMERGENCY ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPOGEUSIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOKINESIA NEONATAL ( 4 FDA reports)
ILEOSTOMY ( 4 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LENTICULAR OPACITIES ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIMB REDUCTION DEFECT ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LOOSE STOOLS ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MELANOSIS COLI ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 4 FDA reports)
METASTASES TO BLADDER ( 4 FDA reports)
METASTASES TO KIDNEY ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MUSCLE FIBROSIS ( 4 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
MYOPATHY TOXIC ( 4 FDA reports)
NASOPHARYNGEAL DISORDER ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEONATAL HYPOXIA ( 4 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NEUROFIBROMA ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
ONCOLOGIC COMPLICATION ( 4 FDA reports)
OPHTHALMOPLEGIA ( 4 FDA reports)
OPTIC NERVE INJURY ( 4 FDA reports)
ORGASM ABNORMAL ( 4 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 4 FDA reports)
OSTEOCHONDROMA ( 4 FDA reports)
OVULATION PAIN ( 4 FDA reports)
PANCREATIC CALCIFICATION ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PARANASAL CYST ( 4 FDA reports)
PARENT-CHILD PROBLEM ( 4 FDA reports)
PATHOGEN RESISTANCE ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
PHAEOCHROMOCYTOMA ( 4 FDA reports)
PHANTOM PAIN ( 4 FDA reports)
PHRENIC NERVE PARALYSIS ( 4 FDA reports)
PILONIDAL CYST CONGENITAL ( 4 FDA reports)
PLEURODESIS ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 4 FDA reports)
POSITIONAL PLAGIOCEPHALY ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POTTER'S SYNDROME ( 4 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 4 FDA reports)
PROTEIN C DECREASED ( 4 FDA reports)
PROTRUSION TONGUE ( 4 FDA reports)
PULMONARY ARTERY ATRESIA ( 4 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 4 FDA reports)
PYLORIC STENOSIS ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RADICULITIS LUMBOSACRAL ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 4 FDA reports)
RENAL AGENESIS ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 4 FDA reports)
RESPIRATORY TRACT IRRITATION ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
RETROGRADE AMNESIA ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SHORT-BOWEL SYNDROME ( 4 FDA reports)
SHUNT MALFUNCTION ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SINUSITIS BACTERIAL ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SKULL FRACTURED BASE ( 4 FDA reports)
SMALL INTESTINAL RESECTION ( 4 FDA reports)
SOCIAL PHOBIA ( 4 FDA reports)
SOFT TISSUE INFLAMMATION ( 4 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
SPLINT APPLICATION ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STASIS DERMATITIS ( 4 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUPPRESSED LACTATION ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TABLET PHYSICAL ISSUE ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TETANY ( 4 FDA reports)
THORACIC HAEMORRHAGE ( 4 FDA reports)
THYROID OPERATION ( 4 FDA reports)
THYROIDECTOMY ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
TUBERCULIN TEST POSITIVE ( 4 FDA reports)
TUMOUR FLARE ( 4 FDA reports)
ULNAR NERVE INJURY ( 4 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 4 FDA reports)
URINARY CASTS ( 4 FDA reports)
URINE CALCIUM DECREASED ( 4 FDA reports)
URINE CANNABINOIDS INCREASED ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE PERFORATION ( 4 FDA reports)
UTERINE RUPTURE ( 4 FDA reports)
VAGINAL ABSCESS ( 4 FDA reports)
VAGINAL BURNING SENSATION ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VAGINAL SWELLING ( 4 FDA reports)
VAGINITIS GARDNERELLA ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VASCULAR SHUNT ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VENOUS STASIS ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VESTIBULAR NEURONITIS ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VISCERAL CONGESTION ( 4 FDA reports)
VITAMIN K DEFICIENCY ( 4 FDA reports)
WAGNER'S DISEASE ( 4 FDA reports)
WEANING FAILURE ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECALL PHENOMENON ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 3 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL OPERATION ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RETINOPATHY OF PREMATURITY ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
SCAR PAIN ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 3 FDA reports)
SCLERODERMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINOBRONCHITIS ( 3 FDA reports)
SKELETON DYSPLASIA ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SOCIAL FEAR ( 3 FDA reports)
SPERM ANALYSIS ABNORMAL ( 3 FDA reports)
SPIDER VEIN ( 3 FDA reports)
SPINA BIFIDA OCCULTA ( 3 FDA reports)
SPLENIC CYST ( 3 FDA reports)
SPLENIC VEIN THROMBOSIS ( 3 FDA reports)
SPOUSAL ABUSE ( 3 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SUSPICIOUSNESS ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
TACHYCARDIA FOETAL ( 3 FDA reports)
TEMPORAL LOBE EPILEPSY ( 3 FDA reports)
THORACIC OPERATION ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TINEA INFECTION ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TONGUE BLACK HAIRY ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONSIL CANCER ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TRACHEAL OBSTRUCTION ( 3 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
TUMOUR RUPTURE ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNDERWEIGHT ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UTERINE MASS ( 3 FDA reports)
VAGINAL OBSTRUCTION ( 3 FDA reports)
VAGINAL PAIN ( 3 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 3 FDA reports)
VASCULAR RUPTURE ( 3 FDA reports)
VASODILATION PROCEDURE ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VERBIGERATION ( 3 FDA reports)
VIBRATION TEST ABNORMAL ( 3 FDA reports)
VIBRATORY SENSE INCREASED ( 3 FDA reports)
VICTIM OF ABUSE ( 3 FDA reports)
VICTIM OF SEXUAL ABUSE ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VITAMIN D INCREASED ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
VOCAL CORD NEOPLASM ( 3 FDA reports)
VULVAR DYSPLASIA ( 3 FDA reports)
WATER INTOXICATION ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABNORMAL LABOUR ( 3 FDA reports)
ABSCESS BACTERIAL ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 3 FDA reports)
ANAL INFLAMMATION ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
APPLICATION SITE EROSION ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AUTOANTIBODY POSITIVE ( 3 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 3 FDA reports)
BENIGN COLONIC POLYP ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BILIARY CYST ( 3 FDA reports)
BINGE EATING ( 3 FDA reports)
BIOPSY BILE DUCT ABNORMAL ( 3 FDA reports)
BLASTOMYCOSIS ( 3 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD CITRIC ACID INCREASED ( 3 FDA reports)
BLOOD ETHANOL INCREASED ( 3 FDA reports)
BLOOD IRON ABNORMAL ( 3 FDA reports)
BLOOD KETONE BODY ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BONE CALLUS EXCESSIVE ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 3 FDA reports)
BREAST CANCER STAGE II ( 3 FDA reports)
BRONCHIAL HYPERACTIVITY ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BURNING SENSATION MUCOSAL ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARCINOMA IN SITU ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC MYXOMA ( 3 FDA reports)
CARDIAC SEPTAL DEFECT ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CATARACT DIABETIC ( 3 FDA reports)
CATECHOLAMINES URINE INCREASED ( 3 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 3 FDA reports)
CEREBRAL HAEMOSIDERIN DEPOSITION ( 3 FDA reports)
CERVICAL CYST ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHALAZION ( 3 FDA reports)
CHEMICAL INJURY ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CHOROIDAL EFFUSION ( 3 FDA reports)
CHRONIC HEPATIC FAILURE ( 3 FDA reports)
CILIARY BODY DISORDER ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
COLON CANCER METASTATIC ( 3 FDA reports)
COLON OPERATION ( 3 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
CONGENITAL BLADDER ANOMALY ( 3 FDA reports)
CONGENITAL HAND MALFORMATION ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
CORNEAL INFILTRATES ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CORNEAL SCAR ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY REVASCULARISATION ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CREATININE URINE INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DELUSION OF GRANDEUR ( 3 FDA reports)
DENGUE FEVER ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
DEVICE DAMAGE ( 3 FDA reports)
DEXTROCARDIA ( 3 FDA reports)
DIABETIC MICROANGIOPATHY ( 3 FDA reports)
DIABETIC RETINAL OEDEMA ( 3 FDA reports)
DIABETIC VASCULAR DISORDER ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
DRUG SCREEN NEGATIVE ( 3 FDA reports)
DRUG THERAPY ( 3 FDA reports)
DUODENAL STENOSIS ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DUODENAL ULCER PERFORATION ( 3 FDA reports)
ELECTRIC SHOCK ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 3 FDA reports)
ENDOCARDITIS BACTERIAL ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EUSTACHIAN TUBE DISORDER ( 3 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 3 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EXOMPHALOS ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYELID PTOSIS CONGENITAL ( 3 FDA reports)
FACE PRESENTATION ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FAMILIAL TREMOR ( 3 FDA reports)
FASCIITIS ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FEMALE ORGASMIC DISORDER ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
FUNGUS URINE TEST POSITIVE ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GENITAL DISORDER MALE ( 3 FDA reports)
GENITAL ERYTHEMA ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
HAEMOPHILUS SEPSIS ( 3 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HEAD DEFORMITY ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HEPATITIS C POSITIVE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HIGH RISK PREGNANCY ( 3 FDA reports)
HUNTINGTON'S DISEASE ( 3 FDA reports)
HYPERCALCIURIA ( 3 FDA reports)
HYPEREMESIS GRAVIDARUM ( 3 FDA reports)
HYPEROXALURIA ( 3 FDA reports)
HYPERSPLENISM ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
INCISION SITE PRURITUS ( 3 FDA reports)
INFANTILE COLIC ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFUSION SITE HAEMORRHAGE ( 3 FDA reports)
INHIBITORY DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE JOINT REDNESS ( 3 FDA reports)
INJECTION SITE SCAB ( 3 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 3 FDA reports)
INTERVERTEBRAL DISCITIS ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JOINT ANKYLOSIS ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LABOUR COMPLICATION ( 3 FDA reports)
LAPAROSCOPY ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LEUKAEMIA PLASMACYTIC ( 3 FDA reports)
LHERMITTE'S SIGN ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MALE SEXUAL DYSFUNCTION ( 3 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MAY-THURNER SYNDROME ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENTAL RETARDATION ( 3 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 3 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 3 FDA reports)
METASTASES TO MENINGES ( 3 FDA reports)
MILIA ( 3 FDA reports)
MITOCHONDRIAL MYOPATHY ( 3 FDA reports)
MITRAL VALVE REPAIR ( 3 FDA reports)
MITRAL VALVE STENOSIS ( 3 FDA reports)
MOEBIUS II SYNDROME ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOROSE ( 3 FDA reports)
MOUTH BREATHING ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NAIL TINEA ( 3 FDA reports)
NASAL SEPTUM PERFORATION ( 3 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 3 FDA reports)
NEAR DROWNING ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEONATAL OVERSEDATION ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEUTRALISING ANTIBODIES ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NIPPLE PAIN ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OCULOGYRATION ( 3 FDA reports)
OESOPHAGEAL DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL DYSPLASIA ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
OESOPHAGEAL OPERATION ( 3 FDA reports)
OESOPHAGEAL PERFORATION ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ONYCHOPHAGIA ( 3 FDA reports)
OPEN FRACTURE ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OROMANDIBULAR DYSTONIA ( 3 FDA reports)
OROPHARYNGEAL SPASM ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PARATHYROID GLAND OPERATION ( 3 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 3 FDA reports)
PARKINSONIAN REST TREMOR ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERIANAL ABSCESS ( 3 FDA reports)
PERIANAL ERYTHEMA ( 3 FDA reports)
PERICARDIAL EXCISION ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PNEUMOBILIA ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POSITIVE ROMBERGISM ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 3 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 3 FDA reports)
POST-TRAUMATIC HEADACHE ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
POSTMATURE BABY ( 3 FDA reports)
POSTOPERATIVE ADHESION ( 3 FDA reports)
PREGNANCY OF PARTNER ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PROCEDURAL DIZZINESS ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PROLONGED EXPIRATION ( 3 FDA reports)
PROSTATECTOMY ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PRURITUS GENITAL ( 3 FDA reports)
PULMONARY BULLA ( 3 FDA reports)
PULMONARY CALCIFICATION ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RADIATION SKIN INJURY ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL WALL CYST ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACROCHORDON EXCISION ( 2 FDA reports)
ACROMEGALY ( 2 FDA reports)
ACUPUNCTURE ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
AMNIOCENTESIS ABNORMAL ( 2 FDA reports)
AMNIOTIC CAVITY DISORDER ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBIOTIC THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 2 FDA reports)
AORTIC ATHEROSCLEROSIS ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARM AMPUTATION ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE ABSCESS ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTIFICIAL MENOPAUSE ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATELECTASIS NEONATAL ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATONIC URINARY BLADDER ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BALANITIS CANDIDA ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BASAL GANGLION DEGENERATION ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASE EXCESS DECREASED ( 2 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
BENIGN UTERINE NEOPLASM ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILOMA ( 2 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 2 FDA reports)
BIOPSY GINGIVAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER AGENESIS ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLEEDING PERIPARTUM ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD HIV RNA INCREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE MARROW PLASMACYTE COUNT INCREASED ( 2 FDA reports)
BONE SCAN ABNORMAL ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BREECH DELIVERY ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
BURSITIS INFECTIVE ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBON DIOXIDE ABNORMAL ( 2 FDA reports)
CARDIAC DISCOMFORT ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC STRESS TEST ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARNITINE DEFICIENCY ( 2 FDA reports)
CAROTID ARTERY BYPASS ( 2 FDA reports)
CAROTID ENDARTERECTOMY ( 2 FDA reports)
CARTILAGE NEOPLASM ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL HAEMANGIOMA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CERULOPLASMIN INCREASED ( 2 FDA reports)
CERVICAL INCOMPETENCE ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRRHOSIS ALCOHOLIC ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSED HEAD INJURY ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPLICATION OF DELIVERY ( 2 FDA reports)
CONCENTRIC SCLEROSIS ( 2 FDA reports)
CONGENITAL AORTIC DILATATION ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 2 FDA reports)
CONJUNCTIVAL CYST ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORONARY ARTERY SURGERY ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYCLIC NEUTROPENIA ( 2 FDA reports)
CYCLOTHYMIC DISORDER ( 2 FDA reports)
CYST REMOVAL ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DENTAL PROSTHESIS USER ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DERMATITIS ARTEFACTA ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE DIFFICULT TO USE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC CYSTOPATHY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC MONONEUROPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DRUG LEVEL ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSPLASIA ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECTOPIC PREGNANCY WITH INTRAUTERINE DEVICE ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENCOPRESIS ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENDOMETRIAL ATROPHY ( 2 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENLARGED UVULA ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EPILEPTIC AURA ( 2 FDA reports)
EPIPHYSEAL DISORDER ( 2 FDA reports)
EPISCLERITIS ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXECUTIVE DYSFUNCTION ( 2 FDA reports)
EXPLORATORY OPERATION ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FACTOR X DEFICIENCY ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FALSE LABOUR ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FIGHT IN SCHOOL ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOREIGN BODY REACTION ( 2 FDA reports)
FRACTURE TREATMENT ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
FUSOBACTERIUM INFECTION ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL INJURY ( 2 FDA reports)
GLIOMA ( 2 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRANULOMA ANNULARE ( 2 FDA reports)
GROWTH ACCELERATED ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HELMINTHIC INFECTION ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HERNIA PAIN ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERTROPHIC SCAR ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMPAIRED REASONING ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE OEDEMA ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFERTILITY ( 2 FDA reports)
INFLAMMATORY PAIN ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE MACULE ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABOUR INDUCTION ( 2 FDA reports)
LACTASE DEFICIENCY ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LASEGUE'S TEST POSITIVE ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGAMENT CALCIFICATION ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP INFECTION ( 2 FDA reports)
LIPASE DECREASED ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 2 FDA reports)
LUNG NEOPLASM SURGERY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MALE PATTERN BALDNESS ( 2 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MASTOID DISORDER ( 2 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEIGE'S SYNDROME ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS NEONATAL ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
METASTASES TO STOMACH ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
METASTATIC OCULAR MELANOMA ( 2 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MIDDLE EAR DISORDER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MONONEURITIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MURPHY'S SIGN POSITIVE ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
NECK SURGERY ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OCULOAURICULOVERTEBRAL DYSPLASIA ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGECTOMY ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
ONYCHORRHEXIS ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL MUCOSAL PETECHIAE ( 2 FDA reports)
ORGASMIC SENSATION DECREASED ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 2 FDA reports)
OXYGEN CONSUMPTION ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATIC PHLEGMON ( 2 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PATIENT RESTRAINT ( 2 FDA reports)
PECTUS EXCAVATUM ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PENILE SWELLING ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVE RASH ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PLEURAL FISTULA ( 2 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 2 FDA reports)
PNEUMONIA NECROTISING ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST POLIO SYNDROME ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL SWELLING ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
POSTOPERATIVE CARE ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROCEDURAL NAUSEA ( 2 FDA reports)
PROCEDURAL VOMITING ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROSTATE CANCER STAGE IV ( 2 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROTEUS INFECTION ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY OEDEMA NEONATAL ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PUPILLARY DEFORMITY ( 2 FDA reports)
PYROMANIA ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RADICAL HYSTERECTOMY ( 2 FDA reports)
RADICULITIS CERVICAL ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL FAILURE NEONATAL ( 2 FDA reports)
RENAL FUNCTION TEST ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL VEIN THROMBOSIS ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL NEOVASCULARISATION ( 2 FDA reports)
RETINAL VASCULITIS ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
RHEUMATOID NODULE REMOVAL ( 2 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 2 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 2 FDA reports)
SCHOOL REFUSAL ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SERUM FERRITIN DECREASED ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SEXUAL ACTIVITY INCREASED ( 2 FDA reports)
SEXUAL OFFENCE ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 2 FDA reports)
SPERMATOGENESIS ABNORMAL ( 2 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLEEN MALFORMATION ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STUBBORNNESS ( 2 FDA reports)
SUBSTANCE ABUSER ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SYRINGOMYELIA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
TESTIS DISCOMFORT ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE ERUPTION ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEAL OEDEMA ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 2 FDA reports)
TRISOMY 8 ( 2 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 2 FDA reports)
TUMOUR MARKER TEST ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERAL DIVERTICULUM ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY BLADDER EXCISION ( 2 FDA reports)
URINARY CYSTECTOMY ( 2 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
UTERINE CERVICAL PAIN ( 2 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 2 FDA reports)
UTERINE PAIN ( 2 FDA reports)
UTEROVAGINAL PROLAPSE ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VAGINISMUS ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
VASCULAR HEADACHE ( 2 FDA reports)
VASCULAR OPERATION ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VICTIM OF HOMICIDE ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VITAMIN D ABNORMAL ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITREOUS DEGENERATION ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WRIST DEFORMITY ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
RADIOISOTOPE SCAN ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER STAGE IV ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM GASTROINTESTINAL TRACT ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIGHT AORTIC ARCH ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCAN BONE MARROW ABNORMAL ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOULDER DEFORMITY ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIALOMETAPLASIA ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLEEP SEX ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPASMODIC DYSPHONIA ( 1 FDA reports)
SPEECH REHABILITATION ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS POLYCYTHAEMIA ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE NEONATAL ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPERIOR MESENTERIC ARTERY SYNDROME ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TAY-SACHS DISEASE ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
THALAMIC SYNDROME ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THANATOPHOBIA ( 1 FDA reports)
THERAPEUTIC ASPIRATION ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TOCOLYSIS ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC DILATATION OF COLON ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC AMPUTATION ( 1 FDA reports)
TRAUMATIC ARTHROPATHY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIGONITIS ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULOSIS BLADDER ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINE BARBITURATES ( 1 FDA reports)
URINE BARBITURATES INCREASED ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
URTICARIA THERMAL ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VASCULAR STENT INSERTION ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR HYPOPLASIA ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VIOLENT IDEATION ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRAL TONSILLITIS ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN A ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D ( 1 FDA reports)
VITAMIN E DECREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL CANCER STAGE III ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINITIS STREPTOCOCCAL ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEST NILE VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
ABDOMINAL AORTIC BRUIT ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE III ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
AORTIC VALVE PROLAPSE ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APGAR SCORE ABNORMAL ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTHROPOD-BORNE DISEASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGER'S DISORDER ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATOPY ( 1 FDA reports)
AURICULAR HAEMATOMA ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOANTIBODY TEST ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AUTOPHONY ( 1 FDA reports)
AUTOPSY ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT CANCER RECURRENT ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 1 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
BIOTIN DEFICIENCY ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BITE ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CALCITONIN DECREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE NORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD LEAD INCREASED ( 1 FDA reports)
BLOOD MERCURY ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THROMBOPLASTIN ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD VISCOSITY INCREASED ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL DYSPLASIA ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BUCCOGLOSSAL SYNDROME ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM METABOLISM DISORDER ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE PHLEBITIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR EMBOLISM ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBROSPINAL FISTULA ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILDHOOD DISINTEGRATIVE DISORDER ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 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)
COGNITIVE DETERIORATION ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON DYSPLASIA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONGENITAL OVARIAN ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL PYELOCALIECTASIS ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONGENITAL TONGUE ANOMALY ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CONTRACEPTIVE DIAPHRAGM ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COW'S MILK INTOLERANCE ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREATINE URINE DECREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEEP BRAIN STIMULATION ( 1 FDA reports)
DEHYDROEPIANDROSTERONE TEST ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED FONTANELLE CLOSURE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES COMPLICATING PREGNANCY ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC CHEIROPATHY ( 1 FDA reports)
DIABETIC DERMOPATHY ( 1 FDA reports)
DIABETIC ENCEPHALOPATHY ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DIVORCED PARENTS ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUPUYTREN'S CONTRACTURE ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EAR OPERATION COMPLICATION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECZEMA EYELIDS ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLIC PNEUMONIA ( 1 FDA reports)
EMERGENCY CARE ( 1 FDA reports)
EMOTIONAL DISORDER OF CHILDHOOD ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
END STAGE AIDS ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 1 FDA reports)
ENDOMETRIAL ABLATION ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENZYME LEVEL DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPINEPHRINE DECREASED ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ETHMOID SINUS SURGERY ( 1 FDA reports)
EXERCISE CAPACITY DECREASED ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRASKELETAL OSSIFICATION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR VII DEFICIENCY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FALLOPIAN TUBE ABSCESS ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLOPPY INFANT ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOETAL ALCOHOL SYNDROME ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE I ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GARDNERELLA TEST POSITIVE ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC CYST ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS PARACOLON BACILLUS ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PAIN MALE ( 1 FDA reports)
GENITAL PRURITUS MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GERSTMANN'S SYNDROME ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED IN PREGNANCY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HABITUAL ABORTION ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEPATECTOMY ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS G ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEREDITARY SPASTIC PARAPLEGIA ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS RECURRENT ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HORMONE THERAPY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPATHIA ( 1 FDA reports)
HYPERSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYSTEROSCOPY ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE PRURITUS ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
INABILITY TO CRAWL ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFESTATION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE CYST ( 1 FDA reports)
INFUSION SITE DERMATITIS ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE MASS ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE PALLOR ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
JAMAIS VU ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KERATITIS SCLEROSING ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KERATOSIS PILARIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LEMIERRE SYNDROME ( 1 FDA reports)
LERICHE SYNDROME ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPIDURIA ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF BLADDER SENSATION ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUMBAR SPINE FLATTENING ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPH NODE ABSCESS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPHOBLAST COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACULE ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 1 FDA reports)
MALIGNANT OLIGODENDROGLIOMA ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MEDIASTINAL ABSCESS ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOPAUSAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METABOLIC FUNCTION TEST ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO OVARY ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO SOFT TISSUE ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MID-LIFE CRISIS ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSAL HYPERAEMIA ( 1 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 1 FDA reports)
MULTIPLE CARDIAC DEFECTS ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
MYOCARDITIS SEPTIC ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING SPINAL CORD ABNORMAL ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL VARICEAL LIGATION ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC DISCS BLURRED ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATOGENOUS DIABETES ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARACENTESIS ABDOMEN ABNORMAL ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPHILIA ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC DEFORMITY ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE PROSTHESIS USER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL CYST ( 1 FDA reports)
PERIORBITAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMA VISCOSITY ABNORMAL ( 1 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA BLASTOMYCES ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONITIS CHEMICAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTOPERATIVE CONSTIPATION ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE CLOSURE OF CRANIAL SUTURES ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROGESTERONE ABNORMAL ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIATION MUCOSITIS ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)