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

ANXIETY ( 1836 FDA reports)
NAUSEA ( 1555 FDA reports)
PAIN ( 1483 FDA reports)
DIZZINESS ( 1453 FDA reports)
COMPLETED SUICIDE ( 1421 FDA reports)
DEPRESSION ( 1376 FDA reports)
FATIGUE ( 1345 FDA reports)
DYSPNOEA ( 1292 FDA reports)
VOMITING ( 1206 FDA reports)
HEADACHE ( 1172 FDA reports)
FALL ( 1164 FDA reports)
CARDIAC ARREST ( 1149 FDA reports)
DRUG INEFFECTIVE ( 1087 FDA reports)
INSOMNIA ( 1077 FDA reports)
DRUG INTERACTION ( 1047 FDA reports)
CONFUSIONAL STATE ( 1032 FDA reports)
PYREXIA ( 1027 FDA reports)
OVERDOSE ( 1017 FDA reports)
MALAISE ( 1000 FDA reports)
DIARRHOEA ( 987 FDA reports)
ASTHENIA ( 980 FDA reports)
SOMNOLENCE ( 937 FDA reports)
TREMOR ( 936 FDA reports)
SUICIDAL IDEATION ( 915 FDA reports)
RESPIRATORY ARREST ( 914 FDA reports)
DRUG TOXICITY ( 865 FDA reports)
WEIGHT DECREASED ( 851 FDA reports)
BACK PAIN ( 829 FDA reports)
CONVULSION ( 829 FDA reports)
HYPERTENSION ( 785 FDA reports)
AGITATION ( 775 FDA reports)
HYPERHIDROSIS ( 766 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 755 FDA reports)
PNEUMONIA ( 747 FDA reports)
CHEST PAIN ( 737 FDA reports)
WEIGHT INCREASED ( 725 FDA reports)
HYPOTENSION ( 702 FDA reports)
DEATH ( 697 FDA reports)
PAIN IN EXTREMITY ( 694 FDA reports)
OEDEMA PERIPHERAL ( 688 FDA reports)
ARTHRALGIA ( 685 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 680 FDA reports)
LOSS OF CONSCIOUSNESS ( 652 FDA reports)
FEELING ABNORMAL ( 646 FDA reports)
PARAESTHESIA ( 645 FDA reports)
SUICIDE ATTEMPT ( 634 FDA reports)
CONSTIPATION ( 631 FDA reports)
CARDIO-RESPIRATORY ARREST ( 613 FDA reports)
CONDITION AGGRAVATED ( 604 FDA reports)
GAIT DISTURBANCE ( 585 FDA reports)
AGGRESSION ( 578 FDA reports)
ANAEMIA ( 567 FDA reports)
URINARY TRACT INFECTION ( 557 FDA reports)
COUGH ( 527 FDA reports)
MUSCLE SPASMS ( 527 FDA reports)
DECREASED APPETITE ( 522 FDA reports)
DIABETES MELLITUS ( 517 FDA reports)
HYPOAESTHESIA ( 514 FDA reports)
ABDOMINAL PAIN ( 512 FDA reports)
MULTIPLE DRUG OVERDOSE ( 512 FDA reports)
INJURY ( 492 FDA reports)
TACHYCARDIA ( 484 FDA reports)
DRUG ABUSE ( 479 FDA reports)
MYALGIA ( 478 FDA reports)
PALPITATIONS ( 475 FDA reports)
VISION BLURRED ( 475 FDA reports)
MEMORY IMPAIRMENT ( 463 FDA reports)
RASH ( 437 FDA reports)
SYNCOPE ( 429 FDA reports)
MYOCARDIAL INFARCTION ( 420 FDA reports)
BLOOD PRESSURE INCREASED ( 413 FDA reports)
HEART RATE INCREASED ( 412 FDA reports)
ABDOMINAL PAIN UPPER ( 408 FDA reports)
DEHYDRATION ( 406 FDA reports)
DISTURBANCE IN ATTENTION ( 406 FDA reports)
PANIC ATTACK ( 405 FDA reports)
AMNESIA ( 396 FDA reports)
BALANCE DISORDER ( 392 FDA reports)
INTENTIONAL OVERDOSE ( 380 FDA reports)
LETHARGY ( 371 FDA reports)
IRRITABILITY ( 367 FDA reports)
PRURITUS ( 367 FDA reports)
COMA ( 365 FDA reports)
SLEEP DISORDER ( 365 FDA reports)
CEREBROVASCULAR ACCIDENT ( 363 FDA reports)
DYSPHAGIA ( 361 FDA reports)
WITHDRAWAL SYNDROME ( 356 FDA reports)
DRY MOUTH ( 344 FDA reports)
EMOTIONAL DISTRESS ( 336 FDA reports)
NIGHTMARE ( 334 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 333 FDA reports)
DYSARTHRIA ( 331 FDA reports)
RESPIRATORY FAILURE ( 326 FDA reports)
HALLUCINATION ( 325 FDA reports)
DISORIENTATION ( 323 FDA reports)
RESTLESSNESS ( 323 FDA reports)
RENAL FAILURE ACUTE ( 320 FDA reports)
DRUG DEPENDENCE ( 319 FDA reports)
OSTEOARTHRITIS ( 319 FDA reports)
PSYCHOTIC DISORDER ( 313 FDA reports)
PULMONARY EMBOLISM ( 312 FDA reports)
DEPRESSED MOOD ( 311 FDA reports)
SPEECH DISORDER ( 308 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 307 FDA reports)
RENAL FAILURE ( 303 FDA reports)
MUSCULAR WEAKNESS ( 302 FDA reports)
CHILLS ( 298 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 296 FDA reports)
ACCIDENTAL OVERDOSE ( 290 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 290 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 289 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 289 FDA reports)
BLOOD GLUCOSE INCREASED ( 287 FDA reports)
DELIRIUM ( 286 FDA reports)
ABNORMAL BEHAVIOUR ( 276 FDA reports)
CONTUSION ( 273 FDA reports)
INTENTIONAL DRUG MISUSE ( 273 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 272 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 272 FDA reports)
NECK PAIN ( 272 FDA reports)
TREATMENT NONCOMPLIANCE ( 270 FDA reports)
BONE DISORDER ( 269 FDA reports)
HAEMOGLOBIN DECREASED ( 269 FDA reports)
MOOD SWINGS ( 269 FDA reports)
POISONING ( 268 FDA reports)
INFLUENZA ( 264 FDA reports)
SEPSIS ( 263 FDA reports)
PULMONARY OEDEMA ( 262 FDA reports)
SEDATION ( 260 FDA reports)
OSTEONECROSIS OF JAW ( 259 FDA reports)
SEROTONIN SYNDROME ( 258 FDA reports)
RESPIRATORY DEPRESSION ( 255 FDA reports)
MIGRAINE ( 254 FDA reports)
CARDIAC DISORDER ( 253 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 252 FDA reports)
ERYTHEMA ( 251 FDA reports)
NEUTROPENIA ( 251 FDA reports)
VERTIGO ( 251 FDA reports)
RHABDOMYOLYSIS ( 246 FDA reports)
ARTHRITIS ( 245 FDA reports)
BRONCHITIS ( 244 FDA reports)
DYSKINESIA ( 243 FDA reports)
DEEP VEIN THROMBOSIS ( 242 FDA reports)
INCORRECT DOSE ADMINISTERED ( 238 FDA reports)
NERVOUSNESS ( 237 FDA reports)
VISUAL IMPAIRMENT ( 237 FDA reports)
SINUS TACHYCARDIA ( 236 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 235 FDA reports)
PLEURAL EFFUSION ( 235 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 233 FDA reports)
ANGER ( 232 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 230 FDA reports)
CARDIOMEGALY ( 230 FDA reports)
MENTAL DISORDER ( 230 FDA reports)
MENTAL STATUS CHANGES ( 230 FDA reports)
THROMBOCYTOPENIA ( 227 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 226 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 223 FDA reports)
MUSCULOSKELETAL PAIN ( 223 FDA reports)
DYSPEPSIA ( 222 FDA reports)
HYPONATRAEMIA ( 220 FDA reports)
PLATELET COUNT DECREASED ( 220 FDA reports)
STRESS ( 220 FDA reports)
ASTHMA ( 218 FDA reports)
BLOOD PRESSURE DECREASED ( 215 FDA reports)
OSTEOMYELITIS ( 214 FDA reports)
SWELLING ( 214 FDA reports)
ARRHYTHMIA ( 213 FDA reports)
INFLUENZA LIKE ILLNESS ( 213 FDA reports)
ROAD TRAFFIC ACCIDENT ( 213 FDA reports)
URINARY INCONTINENCE ( 212 FDA reports)
VISUAL ACUITY REDUCED ( 211 FDA reports)
EMOTIONAL DISORDER ( 211 FDA reports)
COORDINATION ABNORMAL ( 209 FDA reports)
URINARY RETENTION ( 208 FDA reports)
GRAND MAL CONVULSION ( 206 FDA reports)
SINUSITIS ( 204 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 203 FDA reports)
ATRIAL FIBRILLATION ( 202 FDA reports)
HYPOKALAEMIA ( 202 FDA reports)
NEUROPATHY PERIPHERAL ( 202 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 201 FDA reports)
SWELLING FACE ( 200 FDA reports)
DYSPHONIA ( 198 FDA reports)
BRADYCARDIA ( 196 FDA reports)
HYPERSENSITIVITY ( 196 FDA reports)
INFECTION ( 196 FDA reports)
BLOOD CREATININE INCREASED ( 195 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 195 FDA reports)
PARANOIA ( 194 FDA reports)
ABDOMINAL DISTENSION ( 193 FDA reports)
ANHEDONIA ( 193 FDA reports)
STAPHYLOCOCCAL INFECTION ( 191 FDA reports)
TINNITUS ( 191 FDA reports)
TOOTH EXTRACTION ( 191 FDA reports)
CELLULITIS ( 188 FDA reports)
HYPERLIPIDAEMIA ( 185 FDA reports)
ALOPECIA ( 183 FDA reports)
TYPE 2 DIABETES MELLITUS ( 183 FDA reports)
ABNORMAL DREAMS ( 182 FDA reports)
CORONARY ARTERY DISEASE ( 182 FDA reports)
NASOPHARYNGITIS ( 182 FDA reports)
ANOREXIA ( 180 FDA reports)
DYSGEUSIA ( 180 FDA reports)
ABDOMINAL DISCOMFORT ( 179 FDA reports)
CHOLELITHIASIS ( 178 FDA reports)
ABASIA ( 175 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 173 FDA reports)
APHASIA ( 171 FDA reports)
DELUSION ( 171 FDA reports)
ENCEPHALOPATHY ( 171 FDA reports)
FEAR ( 171 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 170 FDA reports)
IMPAIRED HEALING ( 170 FDA reports)
DRUG ABUSER ( 169 FDA reports)
ILL-DEFINED DISORDER ( 169 FDA reports)
MANIA ( 168 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 167 FDA reports)
MULTI-ORGAN FAILURE ( 167 FDA reports)
HEAD INJURY ( 166 FDA reports)
ECONOMIC PROBLEM ( 165 FDA reports)
HALLUCINATION, AUDITORY ( 165 FDA reports)
RECTAL HAEMORRHAGE ( 165 FDA reports)
ASPIRATION ( 164 FDA reports)
PANCREATITIS ( 164 FDA reports)
BURNING SENSATION ( 163 FDA reports)
CHEST DISCOMFORT ( 163 FDA reports)
NEUTROPHIL COUNT INCREASED ( 163 FDA reports)
HAEMORRHAGE ( 161 FDA reports)
HIATUS HERNIA ( 161 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 158 FDA reports)
LYMPHADENOPATHY ( 158 FDA reports)
MOBILITY DECREASED ( 157 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 156 FDA reports)
NYSTAGMUS ( 156 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 155 FDA reports)
METABOLIC ACIDOSIS ( 155 FDA reports)
PULMONARY CONGESTION ( 154 FDA reports)
SPINAL OSTEOARTHRITIS ( 154 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 153 FDA reports)
HEPATIC STEATOSIS ( 153 FDA reports)
PNEUMONIA ASPIRATION ( 153 FDA reports)
TOOTHACHE ( 153 FDA reports)
OSTEOPOROSIS ( 152 FDA reports)
CRYING ( 151 FDA reports)
HYPOXIA ( 151 FDA reports)
JOINT SWELLING ( 151 FDA reports)
MITRAL VALVE INCOMPETENCE ( 151 FDA reports)
OEDEMA ( 151 FDA reports)
ATELECTASIS ( 150 FDA reports)
DRUG HYPERSENSITIVITY ( 150 FDA reports)
LIVER DISORDER ( 150 FDA reports)
MUSCLE TWITCHING ( 149 FDA reports)
PAIN IN JAW ( 149 FDA reports)
CARDIAC FAILURE ( 148 FDA reports)
GASTRITIS ( 148 FDA reports)
OFF LABEL USE ( 148 FDA reports)
SCHIZOPHRENIA ( 148 FDA reports)
HOT FLUSH ( 147 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 143 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 143 FDA reports)
COGNITIVE DISORDER ( 142 FDA reports)
FLUSHING ( 142 FDA reports)
HYPOGLYCAEMIA ( 142 FDA reports)
MEDICATION ERROR ( 142 FDA reports)
RENAL IMPAIRMENT ( 142 FDA reports)
LEUKOPENIA ( 141 FDA reports)
OXYGEN SATURATION DECREASED ( 141 FDA reports)
POOR QUALITY SLEEP ( 141 FDA reports)
URTICARIA ( 141 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 140 FDA reports)
BLOOD POTASSIUM DECREASED ( 140 FDA reports)
OSTEONECROSIS ( 140 FDA reports)
ROTATOR CUFF SYNDROME ( 140 FDA reports)
OROPHARYNGEAL PAIN ( 139 FDA reports)
SUDDEN DEATH ( 139 FDA reports)
WHEEZING ( 139 FDA reports)
ANGINA PECTORIS ( 138 FDA reports)
BLOOD UREA INCREASED ( 138 FDA reports)
HYPERGLYCAEMIA ( 138 FDA reports)
CYANOSIS ( 137 FDA reports)
FEELING JITTERY ( 137 FDA reports)
TOOTH DISORDER ( 136 FDA reports)
UNRESPONSIVE TO STIMULI ( 135 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 135 FDA reports)
INTENTIONAL SELF-INJURY ( 135 FDA reports)
SEPTIC SHOCK ( 135 FDA reports)
AKATHISIA ( 134 FDA reports)
DRUG LEVEL INCREASED ( 134 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 134 FDA reports)
ARTHROPATHY ( 133 FDA reports)
ATAXIA ( 133 FDA reports)
PALLOR ( 133 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 131 FDA reports)
HYPERSOMNIA ( 131 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 131 FDA reports)
POLLAKIURIA ( 130 FDA reports)
CATARACT ( 129 FDA reports)
CARDIAC MURMUR ( 128 FDA reports)
OSTEOPENIA ( 128 FDA reports)
UNEVALUABLE EVENT ( 128 FDA reports)
THINKING ABNORMAL ( 127 FDA reports)
BRAIN OEDEMA ( 126 FDA reports)
DENTAL CARIES ( 126 FDA reports)
MOVEMENT DISORDER ( 126 FDA reports)
DRUG EFFECT DECREASED ( 125 FDA reports)
NERVOUS SYSTEM DISORDER ( 125 FDA reports)
CARDIOVASCULAR DISORDER ( 124 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 124 FDA reports)
CIRCULATORY COLLAPSE ( 123 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 122 FDA reports)
APATHY ( 121 FDA reports)
HYPOAESTHESIA ORAL ( 121 FDA reports)
PULMONARY HYPERTENSION ( 121 FDA reports)
BONE PAIN ( 120 FDA reports)
DRUG DOSE OMISSION ( 120 FDA reports)
HYPOPHAGIA ( 120 FDA reports)
RIB FRACTURE ( 120 FDA reports)
DEVELOPMENTAL DELAY ( 119 FDA reports)
DYSURIA ( 119 FDA reports)
HEART RATE IRREGULAR ( 119 FDA reports)
DYSTONIA ( 118 FDA reports)
NIGHT SWEATS ( 118 FDA reports)
SKIN DISORDER ( 118 FDA reports)
EMPHYSEMA ( 116 FDA reports)
EPILEPSY ( 115 FDA reports)
MENTAL IMPAIRMENT ( 115 FDA reports)
CARDIOMYOPATHY ( 114 FDA reports)
HAEMATOCHEZIA ( 114 FDA reports)
SCAR ( 114 FDA reports)
MULTIPLE INJURIES ( 111 FDA reports)
RESPIRATORY DISTRESS ( 111 FDA reports)
SKIN DISCOLOURATION ( 111 FDA reports)
TEARFULNESS ( 111 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 111 FDA reports)
PANCYTOPENIA ( 110 FDA reports)
BODY TEMPERATURE INCREASED ( 109 FDA reports)
PHYSICAL ASSAULT ( 109 FDA reports)
SALIVARY HYPERSECRETION ( 109 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 109 FDA reports)
BLOOD CALCIUM DECREASED ( 107 FDA reports)
EPISTAXIS ( 107 FDA reports)
MONOCYTE COUNT INCREASED ( 107 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 106 FDA reports)
HEPATIC ENZYME INCREASED ( 106 FDA reports)
MUSCLE RIGIDITY ( 106 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 106 FDA reports)
RENAL DISORDER ( 106 FDA reports)
BRONCHOPNEUMONIA ( 105 FDA reports)
EAR PAIN ( 105 FDA reports)
FISTULA ( 105 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 105 FDA reports)
OBESITY ( 104 FDA reports)
SURGERY ( 104 FDA reports)
TARDIVE DYSKINESIA ( 103 FDA reports)
FEELING HOT ( 103 FDA reports)
GINGIVAL BLEEDING ( 103 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 103 FDA reports)
NEUTROPHIL COUNT DECREASED ( 103 FDA reports)
BLOOD SODIUM DECREASED ( 102 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 101 FDA reports)
INTERSTITIAL LUNG DISEASE ( 101 FDA reports)
LUNG DISORDER ( 101 FDA reports)
SENSORY DISTURBANCE ( 101 FDA reports)
BLISTER ( 100 FDA reports)
PRODUCT QUALITY ISSUE ( 100 FDA reports)
RESTLESS LEGS SYNDROME ( 100 FDA reports)
DIPLOPIA ( 99 FDA reports)
IRON DEFICIENCY ANAEMIA ( 99 FDA reports)
ORAL PAIN ( 99 FDA reports)
POST PROCEDURAL COMPLICATION ( 99 FDA reports)
CEREBRAL INFARCTION ( 98 FDA reports)
HYPOTHYROIDISM ( 98 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 98 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 98 FDA reports)
STOMATITIS ( 98 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 98 FDA reports)
ERECTILE DYSFUNCTION ( 97 FDA reports)
FIBROMYALGIA ( 97 FDA reports)
HAEMATURIA ( 97 FDA reports)
HEART RATE DECREASED ( 97 FDA reports)
JAUNDICE ( 97 FDA reports)
BONE DEBRIDEMENT ( 96 FDA reports)
HERPES ZOSTER ( 96 FDA reports)
MOOD ALTERED ( 96 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 95 FDA reports)
DECREASED INTEREST ( 95 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 95 FDA reports)
EYE PAIN ( 95 FDA reports)
METASTASES TO BONE ( 95 FDA reports)
MULTIPLE SCLEROSIS ( 95 FDA reports)
MYOCLONUS ( 95 FDA reports)
NEPHROLITHIASIS ( 95 FDA reports)
NEOPLASM MALIGNANT ( 94 FDA reports)
PARKINSONISM ( 94 FDA reports)
RENAL FAILURE CHRONIC ( 94 FDA reports)
VISUAL DISTURBANCE ( 94 FDA reports)
HEPATITIS ( 93 FDA reports)
ORTHOSTATIC HYPOTENSION ( 93 FDA reports)
DYSPNOEA EXERTIONAL ( 92 FDA reports)
FOOT FRACTURE ( 92 FDA reports)
INCONTINENCE ( 92 FDA reports)
SUBSTANCE ABUSE ( 92 FDA reports)
THROMBOSIS ( 91 FDA reports)
ALCOHOL USE ( 91 FDA reports)
BLOOD BILIRUBIN INCREASED ( 91 FDA reports)
DEVICE MALFUNCTION ( 91 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 90 FDA reports)
BONE DENSITY DECREASED ( 90 FDA reports)
FLATULENCE ( 90 FDA reports)
LOOSE TOOTH ( 90 FDA reports)
STRABISMUS ( 90 FDA reports)
STATUS EPILEPTICUS ( 89 FDA reports)
CONGENITAL NYSTAGMUS ( 89 FDA reports)
DISSOCIATION ( 89 FDA reports)
HAEMATEMESIS ( 89 FDA reports)
PROTHROMBIN TIME PROLONGED ( 89 FDA reports)
ARTERIOSCLEROSIS ( 88 FDA reports)
DISCOMFORT ( 88 FDA reports)
DIVERTICULUM ( 88 FDA reports)
SHOCK ( 88 FDA reports)
COLONIC POLYP ( 87 FDA reports)
SWOLLEN TONGUE ( 87 FDA reports)
VENTRICULAR TACHYCARDIA ( 86 FDA reports)
VIRAL INFECTION ( 86 FDA reports)
ABSCESS ( 86 FDA reports)
ASCITES ( 86 FDA reports)
INFLAMMATION ( 86 FDA reports)
RESPIRATORY DISORDER ( 86 FDA reports)
HAEMATOCRIT DECREASED ( 85 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 84 FDA reports)
EATING DISORDER ( 84 FDA reports)
FAECAL INCONTINENCE ( 84 FDA reports)
GLAUCOMA ( 83 FDA reports)
LEUKOCYTOSIS ( 83 FDA reports)
MYOCARDIAL ISCHAEMIA ( 83 FDA reports)
TENDERNESS ( 83 FDA reports)
CEREBRAL ATROPHY ( 82 FDA reports)
EYE MOVEMENT DISORDER ( 82 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 82 FDA reports)
MUSCLE ATROPHY ( 82 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 82 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 81 FDA reports)
COLD SWEAT ( 81 FDA reports)
DRY EYE ( 81 FDA reports)
FEMUR FRACTURE ( 81 FDA reports)
HYPERKALAEMIA ( 81 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 81 FDA reports)
RHINITIS ( 81 FDA reports)
THROMBOCYTOSIS ( 81 FDA reports)
INJECTION SITE PAIN ( 80 FDA reports)
INTESTINAL OBSTRUCTION ( 80 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 79 FDA reports)
HEPATOMEGALY ( 79 FDA reports)
SKIN EXFOLIATION ( 79 FDA reports)
ABDOMINAL TENDERNESS ( 78 FDA reports)
DEFORMITY ( 78 FDA reports)
DEPENDENCE ( 78 FDA reports)
HYPERCHOLESTEROLAEMIA ( 78 FDA reports)
PREMATURE BABY ( 78 FDA reports)
PRIMARY SEQUESTRUM ( 78 FDA reports)
SINUS BRADYCARDIA ( 78 FDA reports)
HALLUCINATION, VISUAL ( 77 FDA reports)
HEPATITIS C ( 77 FDA reports)
PHOTOPHOBIA ( 77 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 76 FDA reports)
DIVERTICULUM INTESTINAL ( 76 FDA reports)
LACERATION ( 76 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 76 FDA reports)
PREGNANCY ( 76 FDA reports)
CARPAL TUNNEL SYNDROME ( 75 FDA reports)
DISABILITY ( 75 FDA reports)
FEELING COLD ( 75 FDA reports)
FEELING OF DESPAIR ( 75 FDA reports)
GASTROINTESTINAL DISORDER ( 75 FDA reports)
HEPATIC FAILURE ( 75 FDA reports)
PNEUMOTHORAX ( 75 FDA reports)
BEDRIDDEN ( 74 FDA reports)
SLEEP APNOEA SYNDROME ( 74 FDA reports)
STEVENS-JOHNSON SYNDROME ( 74 FDA reports)
COMA SCALE ABNORMAL ( 73 FDA reports)
EXCORIATION ( 73 FDA reports)
MYDRIASIS ( 73 FDA reports)
PANCREATITIS ACUTE ( 73 FDA reports)
SELF-INJURIOUS IDEATION ( 73 FDA reports)
ACCIDENTAL DEATH ( 72 FDA reports)
HAEMOPTYSIS ( 72 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 72 FDA reports)
POLYNEUROPATHY ( 72 FDA reports)
SENSORY LOSS ( 72 FDA reports)
COAGULOPATHY ( 71 FDA reports)
COGWHEEL RIGIDITY ( 71 FDA reports)
DROOLING ( 71 FDA reports)
HYPERCALCAEMIA ( 71 FDA reports)
ISCHAEMIA ( 71 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 71 FDA reports)
ADVERSE DRUG REACTION ( 70 FDA reports)
APNOEA ( 70 FDA reports)
CEREBRAL HAEMORRHAGE ( 70 FDA reports)
DISEASE PROGRESSION ( 70 FDA reports)
INTENTIONAL MISUSE ( 70 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 70 FDA reports)
NO THERAPEUTIC RESPONSE ( 70 FDA reports)
DRUG SCREEN POSITIVE ( 69 FDA reports)
ECZEMA ( 69 FDA reports)
HIP FRACTURE ( 69 FDA reports)
HYPERTHERMIA ( 69 FDA reports)
GASTRIC DISORDER ( 68 FDA reports)
TOOTH INFECTION ( 68 FDA reports)
BLINDNESS ( 67 FDA reports)
DRY SKIN ( 67 FDA reports)
HEMIPARESIS ( 67 FDA reports)
HYPOTONIA ( 67 FDA reports)
PRESYNCOPE ( 67 FDA reports)
PRURITUS GENERALISED ( 67 FDA reports)
PSYCHIATRIC SYMPTOM ( 67 FDA reports)
ADVERSE EVENT ( 66 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 66 FDA reports)
HOMICIDAL IDEATION ( 66 FDA reports)
HOSPITALISATION ( 66 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 66 FDA reports)
POLYURIA ( 66 FDA reports)
ANKLE FRACTURE ( 65 FDA reports)
INCOHERENT ( 65 FDA reports)
MASTICATION DISORDER ( 65 FDA reports)
NASAL CONGESTION ( 65 FDA reports)
SINUS DISORDER ( 65 FDA reports)
TOOTH ABSCESS ( 65 FDA reports)
VENTRICULAR FIBRILLATION ( 64 FDA reports)
BIPOLAR DISORDER ( 64 FDA reports)
DEAFNESS ( 64 FDA reports)
FACIAL PAIN ( 64 FDA reports)
GALLBLADDER DISORDER ( 64 FDA reports)
HAEMORRHOIDS ( 64 FDA reports)
INCREASED APPETITE ( 64 FDA reports)
JOINT DISLOCATION ( 64 FDA reports)
LUNG NEOPLASM ( 64 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 64 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 64 FDA reports)
COMPRESSION FRACTURE ( 63 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 63 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 62 FDA reports)
JOINT STIFFNESS ( 62 FDA reports)
SKIN ULCER ( 62 FDA reports)
AGRANULOCYTOSIS ( 61 FDA reports)
BLOOD POTASSIUM INCREASED ( 61 FDA reports)
HEARING IMPAIRED ( 61 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 61 FDA reports)
LIMB INJURY ( 61 FDA reports)
MALNUTRITION ( 61 FDA reports)
PANIC REACTION ( 61 FDA reports)
PRODUCTIVE COUGH ( 61 FDA reports)
PULMONARY FIBROSIS ( 61 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 60 FDA reports)
INJECTION SITE ERYTHEMA ( 60 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 60 FDA reports)
IRRITABLE BOWEL SYNDROME ( 60 FDA reports)
MOUTH ULCERATION ( 60 FDA reports)
SUICIDAL BEHAVIOUR ( 60 FDA reports)
ANAPHYLACTIC REACTION ( 59 FDA reports)
HYPERTHYROIDISM ( 59 FDA reports)
JAW DISORDER ( 59 FDA reports)
MUCOSAL INFLAMMATION ( 59 FDA reports)
NOCTURIA ( 59 FDA reports)
ORAL DISCOMFORT ( 59 FDA reports)
PLATELET COUNT INCREASED ( 59 FDA reports)
RASH ERYTHEMATOUS ( 59 FDA reports)
BACK DISORDER ( 58 FDA reports)
DEPERSONALISATION ( 58 FDA reports)
DIABETIC NEUROPATHY ( 58 FDA reports)
DYSSTASIA ( 58 FDA reports)
GASTRIC ULCER ( 58 FDA reports)
GASTROENTERITIS ( 58 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 58 FDA reports)
MUSCLE DISORDER ( 58 FDA reports)
RASH PRURITIC ( 58 FDA reports)
SCOLIOSIS ( 58 FDA reports)
SKIN LESION ( 58 FDA reports)
THYROID NEOPLASM ( 58 FDA reports)
TACHYPNOEA ( 57 FDA reports)
CATATONIA ( 57 FDA reports)
DIABETIC KETOACIDOSIS ( 57 FDA reports)
DISEASE RECURRENCE ( 57 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 57 FDA reports)
GINGIVAL DISORDER ( 57 FDA reports)
JOINT INJURY ( 57 FDA reports)
MEAN CELL VOLUME DECREASED ( 57 FDA reports)
NEURALGIA ( 57 FDA reports)
SOMNAMBULISM ( 57 FDA reports)
LUNG INFILTRATION ( 56 FDA reports)
MIDDLE INSOMNIA ( 56 FDA reports)
OESOPHAGITIS ( 56 FDA reports)
ALCOHOL POISONING ( 55 FDA reports)
BASAL CELL CARCINOMA ( 55 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 55 FDA reports)
BODY MASS INDEX DECREASED ( 55 FDA reports)
FEBRILE NEUTROPENIA ( 55 FDA reports)
FOOT DEFORMITY ( 55 FDA reports)
PERICARDIAL EFFUSION ( 55 FDA reports)
PSORIASIS ( 55 FDA reports)
RESPIRATORY RATE INCREASED ( 55 FDA reports)
RHEUMATOID ARTHRITIS ( 55 FDA reports)
ABORTION SPONTANEOUS ( 54 FDA reports)
BLOOD GLUCOSE DECREASED ( 54 FDA reports)
BREAST CANCER ( 54 FDA reports)
CANDIDIASIS ( 54 FDA reports)
DRUG ERUPTION ( 54 FDA reports)
HYPOTHERMIA ( 54 FDA reports)
PARALYSIS ( 54 FDA reports)
RASH MACULAR ( 54 FDA reports)
SPINAL FRACTURE ( 54 FDA reports)
ACUTE HEPATIC FAILURE ( 53 FDA reports)
BURSITIS ( 53 FDA reports)
DECUBITUS ULCER ( 53 FDA reports)
DRUG ADMINISTRATION ERROR ( 53 FDA reports)
LUNG NEOPLASM MALIGNANT ( 53 FDA reports)
PERSONALITY CHANGE ( 53 FDA reports)
POISONING DELIBERATE ( 53 FDA reports)
PURULENCE ( 53 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 52 FDA reports)
CORONARY ARTERY OCCLUSION ( 52 FDA reports)
CYSTITIS ( 52 FDA reports)
DIVERTICULITIS ( 52 FDA reports)
FRACTURE ( 52 FDA reports)
HEPATIC NECROSIS ( 52 FDA reports)
HYPOKINESIA ( 52 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 52 FDA reports)
PHARYNGEAL OEDEMA ( 52 FDA reports)
AGORAPHOBIA ( 51 FDA reports)
BLOOD ALBUMIN DECREASED ( 51 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 51 FDA reports)
EAR INFECTION ( 51 FDA reports)
GINGIVAL ULCERATION ( 51 FDA reports)
HAEMODIALYSIS ( 51 FDA reports)
HYPOVENTILATION ( 51 FDA reports)
INITIAL INSOMNIA ( 51 FDA reports)
MUSCLE STRAIN ( 51 FDA reports)
PHOTOSENSITIVITY REACTION ( 51 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 51 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 50 FDA reports)
CYST ( 50 FDA reports)
GINGIVITIS ( 50 FDA reports)
METASTASES TO LIVER ( 50 FDA reports)
SNORING ( 50 FDA reports)
ACCIDENT ( 49 FDA reports)
BLOOD UREA DECREASED ( 49 FDA reports)
CAROTID ARTERY STENOSIS ( 49 FDA reports)
EJECTION FRACTION DECREASED ( 49 FDA reports)
ENDODONTIC PROCEDURE ( 49 FDA reports)
HEPATIC CYST ( 49 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 49 FDA reports)
QUALITY OF LIFE DECREASED ( 49 FDA reports)
RESPIRATORY TRACT INFECTION ( 49 FDA reports)
SPINAL DISORDER ( 49 FDA reports)
SPLENOMEGALY ( 49 FDA reports)
TENSION ( 49 FDA reports)
STOMACH DISCOMFORT ( 48 FDA reports)
ATRIAL SEPTAL DEFECT ( 48 FDA reports)
CACHEXIA ( 48 FDA reports)
DEBRIDEMENT ( 48 FDA reports)
DEREALISATION ( 48 FDA reports)
EYELID PTOSIS ( 48 FDA reports)
GENERALISED ANXIETY DISORDER ( 48 FDA reports)
MUSCLE TIGHTNESS ( 48 FDA reports)
ORAL DISORDER ( 48 FDA reports)
OSTEOLYSIS ( 48 FDA reports)
PATHOLOGICAL FRACTURE ( 48 FDA reports)
SINUS CONGESTION ( 48 FDA reports)
SPINAL COLUMN STENOSIS ( 48 FDA reports)
AFFECTIVE DISORDER ( 47 FDA reports)
CROHN'S DISEASE ( 47 FDA reports)
DILATATION VENTRICULAR ( 47 FDA reports)
DISINHIBITION ( 47 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 47 FDA reports)
GINGIVAL INFECTION ( 47 FDA reports)
GYNAECOMASTIA ( 47 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 47 FDA reports)
LIFE EXPECTANCY SHORTENED ( 47 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 47 FDA reports)
PLEURITIC PAIN ( 47 FDA reports)
POSTURE ABNORMAL ( 47 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 47 FDA reports)
RHINORRHOEA ( 47 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 47 FDA reports)
WOUND ( 47 FDA reports)
TENDON DISORDER ( 46 FDA reports)
TOOTH FRACTURE ( 46 FDA reports)
BLOOD URINE PRESENT ( 46 FDA reports)
BONE MARROW FAILURE ( 46 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 46 FDA reports)
LEFT VENTRICULAR FAILURE ( 46 FDA reports)
ORAL CANDIDIASIS ( 46 FDA reports)
POLYDIPSIA ( 46 FDA reports)
PYELONEPHRITIS ( 46 FDA reports)
ACIDOSIS ( 45 FDA reports)
BACTERIAL INFECTION ( 45 FDA reports)
HYPERTONIA ( 45 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 45 FDA reports)
LOCALISED INFECTION ( 45 FDA reports)
MIOSIS ( 45 FDA reports)
RASH GENERALISED ( 45 FDA reports)
RETCHING ( 45 FDA reports)
TOOTH LOSS ( 45 FDA reports)
TUBERCULOSIS ( 45 FDA reports)
TYPE 1 DIABETES MELLITUS ( 44 FDA reports)
URINE OUTPUT DECREASED ( 44 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 44 FDA reports)
VITAMIN D DEFICIENCY ( 44 FDA reports)
WHITE BLOOD CELL DISORDER ( 44 FDA reports)
AMENORRHOEA ( 44 FDA reports)
CEREBRAL ISCHAEMIA ( 44 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 44 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 44 FDA reports)
GINGIVAL RECESSION ( 44 FDA reports)
LOBAR PNEUMONIA ( 44 FDA reports)
MAJOR DEPRESSION ( 44 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 44 FDA reports)
PANIC DISORDER ( 44 FDA reports)
PHYSICAL DISABILITY ( 44 FDA reports)
SCREAMING ( 44 FDA reports)
AREFLEXIA ( 43 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 43 FDA reports)
DEPRESSIVE SYMPTOM ( 43 FDA reports)
GINGIVAL OEDEMA ( 43 FDA reports)
HEPATIC CIRRHOSIS ( 43 FDA reports)
HEPATIC ENCEPHALOPATHY ( 43 FDA reports)
HYPOVOLAEMIA ( 43 FDA reports)
ILEUS ( 43 FDA reports)
IMPAIRED DRIVING ABILITY ( 43 FDA reports)
INFUSION RELATED REACTION ( 43 FDA reports)
JOINT SPRAIN ( 43 FDA reports)
LUNG INFECTION ( 43 FDA reports)
MOTOR DYSFUNCTION ( 43 FDA reports)
MYOPATHY ( 43 FDA reports)
NERVE INJURY ( 43 FDA reports)
PAROSMIA ( 43 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 43 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 43 FDA reports)
TONGUE DISORDER ( 43 FDA reports)
VENTRICULAR HYPERTROPHY ( 43 FDA reports)
THYROID DISORDER ( 42 FDA reports)
CHROMATURIA ( 42 FDA reports)
CREPITATIONS ( 42 FDA reports)
DRUG LEVEL DECREASED ( 42 FDA reports)
DRUG PRESCRIBING ERROR ( 42 FDA reports)
FIBROSIS ( 42 FDA reports)
LIP SWELLING ( 42 FDA reports)
MICTURITION URGENCY ( 42 FDA reports)
OSTEOSCLEROSIS ( 42 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 42 FDA reports)
SKIN BURNING SENSATION ( 42 FDA reports)
SOPOR ( 42 FDA reports)
AFFECT LABILITY ( 41 FDA reports)
ANGINA UNSTABLE ( 41 FDA reports)
CHOLECYSTITIS ( 41 FDA reports)
CHOLECYSTITIS CHRONIC ( 41 FDA reports)
DEMENTIA ( 41 FDA reports)
DRUG INTOLERANCE ( 41 FDA reports)
ELECTROLYTE IMBALANCE ( 41 FDA reports)
EUPHORIC MOOD ( 41 FDA reports)
EYE SWELLING ( 41 FDA reports)
EYELID OEDEMA ( 41 FDA reports)
GLOSSODYNIA ( 41 FDA reports)
HYDROCEPHALUS ( 41 FDA reports)
ILEUS PARALYTIC ( 41 FDA reports)
INADEQUATE ANALGESIA ( 41 FDA reports)
LYMPHOEDEMA ( 41 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 41 FDA reports)
NODULE ( 41 FDA reports)
RENAL CYST ( 41 FDA reports)
THERAPEUTIC PROCEDURE ( 41 FDA reports)
TIBIA FRACTURE ( 41 FDA reports)
SYNOVIAL CYST ( 40 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 40 FDA reports)
UROSEPSIS ( 40 FDA reports)
ACUTE RESPIRATORY FAILURE ( 40 FDA reports)
CEREBELLAR SYNDROME ( 40 FDA reports)
DEAFNESS NEUROSENSORY ( 40 FDA reports)
DIABETIC COMA ( 40 FDA reports)
DIFFICULTY IN WALKING ( 40 FDA reports)
EMPYEMA ( 40 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 40 FDA reports)
EYE DISORDER ( 40 FDA reports)
FUNGAL INFECTION ( 40 FDA reports)
HYPERVENTILATION ( 40 FDA reports)
HYPOAESTHESIA FACIAL ( 40 FDA reports)
HYPOCALCAEMIA ( 40 FDA reports)
OSTEITIS ( 40 FDA reports)
PHARYNGITIS ( 40 FDA reports)
AORTIC ANEURYSM ( 39 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 39 FDA reports)
BACK INJURY ( 39 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 39 FDA reports)
CONJUNCTIVITIS ( 39 FDA reports)
FORMICATION ( 39 FDA reports)
H1N1 INFLUENZA ( 39 FDA reports)
HALLUCINATIONS, MIXED ( 39 FDA reports)
HYPERTENSIVE HEART DISEASE ( 39 FDA reports)
HYPOACUSIS ( 39 FDA reports)
LIMB DISCOMFORT ( 39 FDA reports)
MASS ( 39 FDA reports)
MELAENA ( 39 FDA reports)
MICROCEPHALY ( 39 FDA reports)
PLEURAL FIBROSIS ( 39 FDA reports)
RESPIRATORY RATE DECREASED ( 39 FDA reports)
SCIATICA ( 39 FDA reports)
SELF-MEDICATION ( 39 FDA reports)
THROAT TIGHTNESS ( 39 FDA reports)
THIRST ( 38 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 38 FDA reports)
CAESAREAN SECTION ( 38 FDA reports)
CHOLESTASIS ( 38 FDA reports)
DEVICE FAILURE ( 38 FDA reports)
DYSLIPIDAEMIA ( 38 FDA reports)
FEELING DRUNK ( 38 FDA reports)
FLANK PAIN ( 38 FDA reports)
GOITRE ( 38 FDA reports)
HEPATIC CONGESTION ( 38 FDA reports)
HOSTILITY ( 38 FDA reports)
LIVER INJURY ( 38 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 38 FDA reports)
MENSTRUAL DISORDER ( 38 FDA reports)
PERIPHERAL COLDNESS ( 38 FDA reports)
PREMATURE LABOUR ( 38 FDA reports)
PULSE ABSENT ( 38 FDA reports)
RESUSCITATION ( 38 FDA reports)
BREAST CANCER FEMALE ( 37 FDA reports)
BRONCHOSPASM ( 37 FDA reports)
CHOKING ( 37 FDA reports)
CHONDROMALACIA ( 37 FDA reports)
CORONARY ARTERY STENOSIS ( 37 FDA reports)
DIALYSIS ( 37 FDA reports)
DYSPHEMIA ( 37 FDA reports)
EOSINOPHILIA ( 37 FDA reports)
HAND FRACTURE ( 37 FDA reports)
HEPATITIS ACUTE ( 37 FDA reports)
HYDRONEPHROSIS ( 37 FDA reports)
HYPERPROLACTINAEMIA ( 37 FDA reports)
LABORATORY TEST ABNORMAL ( 37 FDA reports)
METASTASES TO LYMPH NODES ( 37 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 37 FDA reports)
PSEUDOMONAS INFECTION ( 37 FDA reports)
ACUTE SINUSITIS ( 36 FDA reports)
ANXIETY DISORDER ( 36 FDA reports)
ASPHYXIA ( 36 FDA reports)
BLOOD AMYLASE INCREASED ( 36 FDA reports)
CLEFT PALATE ( 36 FDA reports)
CONVERSION DISORDER ( 36 FDA reports)
DECREASED ACTIVITY ( 36 FDA reports)
HAEMATOMA ( 36 FDA reports)
HYPOCHONDRIASIS ( 36 FDA reports)
HYSTERECTOMY ( 36 FDA reports)
IMPAIRED WORK ABILITY ( 36 FDA reports)
LIBIDO DECREASED ( 36 FDA reports)
MYOSITIS ( 36 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 36 FDA reports)
OEDEMA MOUTH ( 36 FDA reports)
OVARIAN CYST ( 36 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 36 FDA reports)
PERIODONTAL DISEASE ( 36 FDA reports)
RENAL TUBULAR NECROSIS ( 36 FDA reports)
RHONCHI ( 36 FDA reports)
SPINAL COMPRESSION FRACTURE ( 36 FDA reports)
THERMAL BURN ( 36 FDA reports)
VASCULITIS ( 36 FDA reports)
VIITH NERVE PARALYSIS ( 36 FDA reports)
THROAT IRRITATION ( 35 FDA reports)
UPPER LIMB FRACTURE ( 35 FDA reports)
ATRIAL FLUTTER ( 35 FDA reports)
BLOOD PH DECREASED ( 35 FDA reports)
BLOOD PROLACTIN INCREASED ( 35 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 35 FDA reports)
EOSINOPHIL COUNT INCREASED ( 35 FDA reports)
FAMILY STRESS ( 35 FDA reports)
HERNIA ( 35 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 35 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 35 FDA reports)
KYPHOSCOLIOSIS ( 35 FDA reports)
MYOCARDITIS ( 35 FDA reports)
NARCOTIC INTOXICATION ( 35 FDA reports)
PARAESTHESIA ORAL ( 35 FDA reports)
PLEUROTHOTONUS ( 35 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 35 FDA reports)
PURULENT DISCHARGE ( 35 FDA reports)
ABSCESS JAW ( 34 FDA reports)
ACNE ( 34 FDA reports)
ANAPHYLACTIC SHOCK ( 34 FDA reports)
AORTIC VALVE INCOMPETENCE ( 34 FDA reports)
BREAST PAIN ( 34 FDA reports)
CLUMSINESS ( 34 FDA reports)
DEVICE RELATED INFECTION ( 34 FDA reports)
EYE DISCHARGE ( 34 FDA reports)
LOSS OF LIBIDO ( 34 FDA reports)
METASTASES TO SPINE ( 34 FDA reports)
MULTIPLE MYELOMA ( 34 FDA reports)
NECROSIS ( 34 FDA reports)
NERVE COMPRESSION ( 34 FDA reports)
OROPHARYNGEAL PLAQUE ( 34 FDA reports)
PARKINSON'S DISEASE ( 34 FDA reports)
SEQUESTRECTOMY ( 34 FDA reports)
SKIN LACERATION ( 34 FDA reports)
TENDONITIS ( 34 FDA reports)
WOUND DEHISCENCE ( 34 FDA reports)
THERAPY NON-RESPONDER ( 33 FDA reports)
TRAUMATIC BRAIN INJURY ( 33 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 33 FDA reports)
UTERINE LEIOMYOMA ( 33 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 33 FDA reports)
BONE SCAN ABNORMAL ( 33 FDA reports)
BRUXISM ( 33 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 33 FDA reports)
HYPERTENSIVE CRISIS ( 33 FDA reports)
HYPOALBUMINAEMIA ( 33 FDA reports)
HYPOMANIA ( 33 FDA reports)
INJECTION SITE HAEMATOMA ( 33 FDA reports)
JOINT EFFUSION ( 33 FDA reports)
KIDNEY INFECTION ( 33 FDA reports)
KYPHOSIS ( 33 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 33 FDA reports)
ORAL HERPES ( 33 FDA reports)
PERITONITIS ( 33 FDA reports)
RALES ( 33 FDA reports)
ABSCESS DRAINAGE ( 32 FDA reports)
ANEURYSM ( 32 FDA reports)
ANGIOEDEMA ( 32 FDA reports)
BLOOD PRESSURE ABNORMAL ( 32 FDA reports)
DERMATITIS ( 32 FDA reports)
GINGIVAL SWELLING ( 32 FDA reports)
HYPERREFLEXIA ( 32 FDA reports)
INJECTION SITE HAEMORRHAGE ( 32 FDA reports)
MENISCUS LESION ( 32 FDA reports)
MUSCLE SPASTICITY ( 32 FDA reports)
OPTIC NERVE HYPOPLASIA ( 32 FDA reports)
RESPIRATORY ACIDOSIS ( 32 FDA reports)
SENSATION OF HEAVINESS ( 32 FDA reports)
SLUGGISHNESS ( 32 FDA reports)
STREPTOCOCCAL INFECTION ( 32 FDA reports)
TOBACCO USER ( 32 FDA reports)
STRIDOR ( 31 FDA reports)
TOXIC ENCEPHALOPATHY ( 31 FDA reports)
ULCER ( 31 FDA reports)
VITREOUS FLOATERS ( 31 FDA reports)
WALKING AID USER ( 31 FDA reports)
ABDOMINAL PAIN LOWER ( 31 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 31 FDA reports)
ARTHROSCOPY ( 31 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 31 FDA reports)
BLOOD LACTIC ACID INCREASED ( 31 FDA reports)
BRADYPHRENIA ( 31 FDA reports)
COLITIS ( 31 FDA reports)
DUODENITIS ( 31 FDA reports)
ESCHERICHIA INFECTION ( 31 FDA reports)
GASTRIC HAEMORRHAGE ( 31 FDA reports)
GASTRIC PH DECREASED ( 31 FDA reports)
GRANULOMA ( 31 FDA reports)
HAEMOTHORAX ( 31 FDA reports)
INJECTION SITE REACTION ( 31 FDA reports)
LOCAL SWELLING ( 31 FDA reports)
MENSTRUATION IRREGULAR ( 31 FDA reports)
METASTATIC NEOPLASM ( 31 FDA reports)
ORAL SURGERY ( 31 FDA reports)
RADICULOPATHY ( 31 FDA reports)
RASH PAPULAR ( 31 FDA reports)
ANURIA ( 30 FDA reports)
ATRIOVENTRICULAR BLOCK ( 30 FDA reports)
BLADDER DISORDER ( 30 FDA reports)
BLOOD BICARBONATE DECREASED ( 30 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 30 FDA reports)
CATARACT OPERATION ( 30 FDA reports)
CHRONIC SINUSITIS ( 30 FDA reports)
CLAVICLE FRACTURE ( 30 FDA reports)
COLONOSCOPY ( 30 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 30 FDA reports)
FAILURE TO THRIVE ( 30 FDA reports)
HYPERCOAGULATION ( 30 FDA reports)
INCISIONAL DRAINAGE ( 30 FDA reports)
JAW OPERATION ( 30 FDA reports)
LACRIMATION INCREASED ( 30 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 30 FDA reports)
OCULAR HYPERAEMIA ( 30 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 30 FDA reports)
PETIT MAL EPILEPSY ( 30 FDA reports)
SENSITIVITY OF TEETH ( 30 FDA reports)
SEXUAL DYSFUNCTION ( 30 FDA reports)
SPINAL FUSION SURGERY ( 30 FDA reports)
STUPOR ( 30 FDA reports)
TROPONIN INCREASED ( 30 FDA reports)
TORSADE DE POINTES ( 29 FDA reports)
ANGIOPATHY ( 29 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 29 FDA reports)
EXOSTOSIS ( 29 FDA reports)
EXPIRED DRUG ADMINISTERED ( 29 FDA reports)
EYE IRRITATION ( 29 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 29 FDA reports)
FRACTURED SACRUM ( 29 FDA reports)
HEPATOTOXICITY ( 29 FDA reports)
HUMERUS FRACTURE ( 29 FDA reports)
HYPERTONIC BLADDER ( 29 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 29 FDA reports)
LACTIC ACIDOSIS ( 29 FDA reports)
LARYNGEAL OEDEMA ( 29 FDA reports)
MENORRHAGIA ( 29 FDA reports)
MULTIPLE ALLERGIES ( 29 FDA reports)
NEUROGENIC BLADDER ( 29 FDA reports)
PNEUMONITIS ( 29 FDA reports)
PULMONARY HAEMORRHAGE ( 29 FDA reports)
RASH MACULO-PAPULAR ( 29 FDA reports)
REFLUX OESOPHAGITIS ( 29 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 28 FDA reports)
CERVICAL SPINAL STENOSIS ( 28 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 28 FDA reports)
FAECALOMA ( 28 FDA reports)
HYPERACUSIS ( 28 FDA reports)
HYPERPHAGIA ( 28 FDA reports)
INJECTION SITE SWELLING ( 28 FDA reports)
METABOLIC SYNDROME ( 28 FDA reports)
MUCOSAL DRYNESS ( 28 FDA reports)
NON-CARDIAC CHEST PAIN ( 28 FDA reports)
PELVIC FRACTURE ( 28 FDA reports)
SPLINTER ( 28 FDA reports)
SUTURE INSERTION ( 28 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 28 FDA reports)
ALCOHOLISM ( 27 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 27 FDA reports)
ATRIAL TACHYCARDIA ( 27 FDA reports)
BLOOD ALCOHOL INCREASED ( 27 FDA reports)
BONE LESION ( 27 FDA reports)
BREAST MASS ( 27 FDA reports)
CATARACT NUCLEAR ( 27 FDA reports)
CRYSTALLURIA ( 27 FDA reports)
DROWNING ( 27 FDA reports)
FLAT AFFECT ( 27 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 27 FDA reports)
GENERALISED OEDEMA ( 27 FDA reports)
GINGIVAL HYPERPLASIA ( 27 FDA reports)
HEPATOSPLENOMEGALY ( 27 FDA reports)
HICCUPS ( 27 FDA reports)
HOMICIDE ( 27 FDA reports)
HYPERPYREXIA ( 27 FDA reports)
HYPOMAGNESAEMIA ( 27 FDA reports)
INJURY ASPHYXIATION ( 27 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 27 FDA reports)
KETOACIDOSIS ( 27 FDA reports)
METABOLIC ENCEPHALOPATHY ( 27 FDA reports)
OSTEORADIONECROSIS ( 27 FDA reports)
POLYSUBSTANCE ABUSE ( 27 FDA reports)
PRESCRIBED OVERDOSE ( 27 FDA reports)
PROCEDURAL COMPLICATION ( 27 FDA reports)
RHINITIS ALLERGIC ( 27 FDA reports)
ROTATOR CUFF REPAIR ( 27 FDA reports)
SJOGREN'S SYNDROME ( 27 FDA reports)
ADJUSTMENT DISORDER ( 26 FDA reports)
BLOOD CREATININE DECREASED ( 26 FDA reports)
BONE LOSS ( 26 FDA reports)
CARDIAC VALVE DISEASE ( 26 FDA reports)
CARDIOGENIC SHOCK ( 26 FDA reports)
CHOLECYSTECTOMY ( 26 FDA reports)
COMMUNICATION DISORDER ( 26 FDA reports)
DENTURE WEARER ( 26 FDA reports)
DYSPHORIA ( 26 FDA reports)
GINGIVAL PAIN ( 26 FDA reports)
GROIN PAIN ( 26 FDA reports)
HUNGER ( 26 FDA reports)
HYPERAEMIA ( 26 FDA reports)
IMPULSIVE BEHAVIOUR ( 26 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 26 FDA reports)
LARYNGOSPASM ( 26 FDA reports)
METRORRHAGIA ( 26 FDA reports)
NIKOLSKY'S SIGN ( 26 FDA reports)
NO ADVERSE EVENT ( 26 FDA reports)
PELVIC PAIN ( 26 FDA reports)
PERIARTHRITIS ( 26 FDA reports)
PERONEAL NERVE PALSY ( 26 FDA reports)
POLYP ( 26 FDA reports)
PROTEIN TOTAL DECREASED ( 26 FDA reports)
RENAL INJURY ( 26 FDA reports)
SKIN IRRITATION ( 26 FDA reports)
SOCIAL PROBLEM ( 26 FDA reports)
TENDON RUPTURE ( 26 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 26 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 25 FDA reports)
URINE ODOUR ABNORMAL ( 25 FDA reports)
VAGINAL HAEMORRHAGE ( 25 FDA reports)
ACCIDENTAL EXPOSURE ( 25 FDA reports)
ACCIDENTAL POISONING ( 25 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 25 FDA reports)
CEREBROVASCULAR DISORDER ( 25 FDA reports)
DROP ATTACKS ( 25 FDA reports)
ENURESIS ( 25 FDA reports)
EXPOSED BONE IN JAW ( 25 FDA reports)
FAECES DISCOLOURED ( 25 FDA reports)
FLUID RETENTION ( 25 FDA reports)
FORAMEN MAGNUM STENOSIS ( 25 FDA reports)
FRUSTRATION ( 25 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 25 FDA reports)
GOUT ( 25 FDA reports)
HYPERPARATHYROIDISM ( 25 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 25 FDA reports)
IMMUNODEFICIENCY ( 25 FDA reports)
INCREASED TENDENCY TO BRUISE ( 25 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 25 FDA reports)
JOINT CREPITATION ( 25 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 25 FDA reports)
NEONATAL DISORDER ( 25 FDA reports)
RENAL PAIN ( 25 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 25 FDA reports)
AMMONIA INCREASED ( 24 FDA reports)
ANTISOCIAL BEHAVIOUR ( 24 FDA reports)
AORTIC DISORDER ( 24 FDA reports)
BACTERIA URINE ( 24 FDA reports)
BLOOD BICARBONATE INCREASED ( 24 FDA reports)
BRAIN HERNIATION ( 24 FDA reports)
BREATH ODOUR ( 24 FDA reports)
CHOLINERGIC SYNDROME ( 24 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 24 FDA reports)
DERMATITIS ALLERGIC ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 24 FDA reports)
HEAD DISCOMFORT ( 24 FDA reports)
HEPATOCELLULAR DAMAGE ( 24 FDA reports)
KNEE ARTHROPLASTY ( 24 FDA reports)
KNEE OPERATION ( 24 FDA reports)
LIPIDS INCREASED ( 24 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 24 FDA reports)
MALLORY-WEISS SYNDROME ( 24 FDA reports)
NEPHROPATHY TOXIC ( 24 FDA reports)
NERVE BLOCK ( 24 FDA reports)
SPLEEN CONGESTION ( 24 FDA reports)
VITAMIN D DECREASED ( 24 FDA reports)
SUBDURAL HAEMATOMA ( 23 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 23 FDA reports)
SUSPICIOUSNESS ( 23 FDA reports)
TONGUE BITING ( 23 FDA reports)
TOOTH IMPACTED ( 23 FDA reports)
TREATMENT FAILURE ( 23 FDA reports)
URINE OUTPUT INCREASED ( 23 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 23 FDA reports)
ACUTE PULMONARY OEDEMA ( 23 FDA reports)
APPLICATION SITE ERYTHEMA ( 23 FDA reports)
BLADDER CANCER RECURRENT ( 23 FDA reports)
BLOOD CHLORIDE DECREASED ( 23 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 23 FDA reports)
CATHETER RELATED COMPLICATION ( 23 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 23 FDA reports)
COSTOCHONDRITIS ( 23 FDA reports)
DEMYELINATION ( 23 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 23 FDA reports)
FIBULA FRACTURE ( 23 FDA reports)
GALACTORRHOEA ( 23 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 23 FDA reports)
HAEMODYNAMIC INSTABILITY ( 23 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 23 FDA reports)
LOSS OF EMPLOYMENT ( 23 FDA reports)
LYMPHOCYTOSIS ( 23 FDA reports)
METASTASIS ( 23 FDA reports)
MUTISM ( 23 FDA reports)
NASAL ULCER ( 23 FDA reports)
NEGATIVE THOUGHTS ( 23 FDA reports)
ORTHOPNOEA ( 23 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 23 FDA reports)
PERSECUTORY DELUSION ( 23 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 23 FDA reports)
PRODUCT ADHESION ISSUE ( 23 FDA reports)
RADIUS FRACTURE ( 23 FDA reports)
RESORPTION BONE INCREASED ( 23 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 23 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 23 FDA reports)
SINUS OPERATION ( 23 FDA reports)
SKIN INDURATION ( 23 FDA reports)
ADRENAL INSUFFICIENCY ( 22 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 22 FDA reports)
APHTHOUS STOMATITIS ( 22 FDA reports)
APLASTIC ANAEMIA ( 22 FDA reports)
ATHEROSCLEROSIS ( 22 FDA reports)
BENIGN COLONIC NEOPLASM ( 22 FDA reports)
BILE DUCT STONE ( 22 FDA reports)
BODY HEIGHT DECREASED ( 22 FDA reports)
CARDIOPULMONARY FAILURE ( 22 FDA reports)
CHEST X-RAY ABNORMAL ( 22 FDA reports)
CHOKING SENSATION ( 22 FDA reports)
CLAUSTROPHOBIA ( 22 FDA reports)
DENTAL IMPLANTATION ( 22 FDA reports)
DERMAL CYST ( 22 FDA reports)
DRUG EFFECT INCREASED ( 22 FDA reports)
ENTEROCOCCAL INFECTION ( 22 FDA reports)
ERUCTATION ( 22 FDA reports)
FACE OEDEMA ( 22 FDA reports)
FACIAL PALSY ( 22 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 22 FDA reports)
GASTRITIS EROSIVE ( 22 FDA reports)
GASTROENTERITIS VIRAL ( 22 FDA reports)
GRANULOCYTOPENIA ( 22 FDA reports)
HYPERMETROPIA ( 22 FDA reports)
HYPERNATRAEMIA ( 22 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 22 FDA reports)
LOWER LIMB FRACTURE ( 22 FDA reports)
LUMBAR SPINAL STENOSIS ( 22 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 22 FDA reports)
MACROCYTOSIS ( 22 FDA reports)
MASKED FACIES ( 22 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 22 FDA reports)
NASAL DISORDER ( 22 FDA reports)
PLANTAR FASCIITIS ( 22 FDA reports)
PUPILS UNEQUAL ( 22 FDA reports)
RAYNAUD'S PHENOMENON ( 22 FDA reports)
SARCOIDOSIS ( 22 FDA reports)
SCAB ( 22 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 22 FDA reports)
SKIN HYPERTROPHY ( 22 FDA reports)
SKIN INFECTION ( 22 FDA reports)
SPINAL DEFORMITY ( 22 FDA reports)
TRANSAMINASES INCREASED ( 22 FDA reports)
VASCULAR INJURY ( 22 FDA reports)
WOUND INFECTION ( 22 FDA reports)
SUDDEN CARDIAC DEATH ( 21 FDA reports)
TELANGIECTASIA ( 21 FDA reports)
TONGUE ULCERATION ( 21 FDA reports)
TRISMUS ( 21 FDA reports)
VENOUS INSUFFICIENCY ( 21 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 21 FDA reports)
ALCOHOL ABUSE ( 21 FDA reports)
ANION GAP INCREASED ( 21 FDA reports)
APHONIA ( 21 FDA reports)
APNOEIC ATTACK ( 21 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 21 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 21 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 21 FDA reports)
CHOLECYSTITIS ACUTE ( 21 FDA reports)
COLITIS ULCERATIVE ( 21 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 21 FDA reports)
DRUG DISPENSING ERROR ( 21 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 21 FDA reports)
DRUG TOLERANCE ( 21 FDA reports)
EXERCISE TOLERANCE DECREASED ( 21 FDA reports)
FLASHBACK ( 21 FDA reports)
GENERALISED ERYTHEMA ( 21 FDA reports)
HEART RATE ABNORMAL ( 21 FDA reports)
HELICOBACTER INFECTION ( 21 FDA reports)
HYPERBILIRUBINAEMIA ( 21 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 21 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 21 FDA reports)
LUMBAR RADICULOPATHY ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MORBID THOUGHTS ( 21 FDA reports)
NEPHROSCLEROSIS ( 21 FDA reports)
PAIN OF SKIN ( 21 FDA reports)
PANNICULITIS ( 21 FDA reports)
PERFORATED ULCER ( 21 FDA reports)
PHOTOPSIA ( 21 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 21 FDA reports)
PURPURA ( 21 FDA reports)
SKIN CHAPPED ( 21 FDA reports)
SKIN TIGHTNESS ( 21 FDA reports)
SPONDYLOARTHROPATHY ( 21 FDA reports)
AKINESIA ( 20 FDA reports)
ALCOHOL INTERACTION ( 20 FDA reports)
APPLICATION SITE IRRITATION ( 20 FDA reports)
ASPERGILLOSIS ( 20 FDA reports)
BACTERAEMIA ( 20 FDA reports)
BLEPHAROSPASM ( 20 FDA reports)
BODY TEMPERATURE DECREASED ( 20 FDA reports)
BREAST CANCER METASTATIC ( 20 FDA reports)
EROSIVE OESOPHAGITIS ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
EXTRASYSTOLES ( 20 FDA reports)
FACET JOINT SYNDROME ( 20 FDA reports)
HEMIPLEGIA ( 20 FDA reports)
HIP ARTHROPLASTY ( 20 FDA reports)
ILLUSION ( 20 FDA reports)
LARYNGITIS ( 20 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 20 FDA reports)
MELANOCYTIC NAEVUS ( 20 FDA reports)
MORTON'S NEUROMA ( 20 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 20 FDA reports)
NEUROPATHY ( 20 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
PARAPLEGIA ( 20 FDA reports)
PLEURISY ( 20 FDA reports)
PUPIL FIXED ( 20 FDA reports)
RENAL COLIC ( 20 FDA reports)
SACROILIITIS ( 20 FDA reports)
SINUS HEADACHE ( 20 FDA reports)
SOFT TISSUE DISORDER ( 20 FDA reports)
SPUTUM DISCOLOURED ( 20 FDA reports)
SQUAMOUS CELL CARCINOMA ( 20 FDA reports)
STRABISMUS CONGENITAL ( 20 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 20 FDA reports)
THYROXINE FREE DECREASED ( 20 FDA reports)
WRIST FRACTURE ( 20 FDA reports)
STRESS FRACTURE ( 19 FDA reports)
STRESS URINARY INCONTINENCE ( 19 FDA reports)
TEMPERATURE INTOLERANCE ( 19 FDA reports)
TENSION HEADACHE ( 19 FDA reports)
THROMBOPHLEBITIS ( 19 FDA reports)
TOOTH DEPOSIT ( 19 FDA reports)
TORTICOLLIS ( 19 FDA reports)
TRIGEMINAL NEURALGIA ( 19 FDA reports)
UTERINE DISORDER ( 19 FDA reports)
VARICOSE VEIN ( 19 FDA reports)
ADRENAL MASS ( 19 FDA reports)
ARTHRITIS BACTERIAL ( 19 FDA reports)
BACTERIAL DISEASE CARRIER ( 19 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 19 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 19 FDA reports)
BONE EROSION ( 19 FDA reports)
CARDIAC DEATH ( 19 FDA reports)
COMPLEX PARTIAL SEIZURES ( 19 FDA reports)
DUODENAL ULCER PERFORATION ( 19 FDA reports)
DYSTHYMIC DISORDER ( 19 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 19 FDA reports)
FIBRIN D DIMER INCREASED ( 19 FDA reports)
FOETAL DISTRESS SYNDROME ( 19 FDA reports)
GANGRENE ( 19 FDA reports)
GASTRIC POLYPS ( 19 FDA reports)
HYPERAESTHESIA ( 19 FDA reports)
HYPERTROPHY ( 19 FDA reports)
INGUINAL HERNIA ( 19 FDA reports)
LYMPHOMA ( 19 FDA reports)
MACULAR DEGENERATION ( 19 FDA reports)
MACULAR OEDEMA ( 19 FDA reports)
METABOLIC DISORDER ( 19 FDA reports)
METASTASES TO LUNG ( 19 FDA reports)
MITRAL VALVE PROLAPSE ( 19 FDA reports)
NEUROTOXICITY ( 19 FDA reports)
NODAL RHYTHM ( 19 FDA reports)
OPTIC NEURITIS ( 19 FDA reports)
PEPTIC ULCER ( 19 FDA reports)
PETECHIAE ( 19 FDA reports)
PO2 DECREASED ( 19 FDA reports)
QUADRIPARESIS ( 19 FDA reports)
RADICULAR PAIN ( 19 FDA reports)
RIGHT ATRIAL DILATATION ( 19 FDA reports)
SHOULDER PAIN ( 19 FDA reports)
SPINAL DECOMPRESSION ( 19 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
ANAESTHETIC COMPLICATION ( 18 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 18 FDA reports)
APHAGIA ( 18 FDA reports)
APPLICATION SITE RASH ( 18 FDA reports)
ARTERIAL DISORDER ( 18 FDA reports)
BLINDNESS TRANSIENT ( 18 FDA reports)
BLOOD FOLATE INCREASED ( 18 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 18 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 18 FDA reports)
BLOOD SODIUM INCREASED ( 18 FDA reports)
BRADYKINESIA ( 18 FDA reports)
BRAIN DEATH ( 18 FDA reports)
CALCIUM DEFICIENCY ( 18 FDA reports)
COLONOSCOPY ABNORMAL ( 18 FDA reports)
CSF PROTEIN INCREASED ( 18 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 18 FDA reports)
DIABETIC COMPLICATION ( 18 FDA reports)
DIASTOLIC DYSFUNCTION ( 18 FDA reports)
EAR HAEMORRHAGE ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 18 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 18 FDA reports)
EXCESSIVE EYE BLINKING ( 18 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 18 FDA reports)
FLUID OVERLOAD ( 18 FDA reports)
HEARING AID USER ( 18 FDA reports)
HEPATIC LESION ( 18 FDA reports)
HYPERALDOSTERONISM ( 18 FDA reports)
HYPERCAPNIA ( 18 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 18 FDA reports)
INTERMITTENT CLAUDICATION ( 18 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 18 FDA reports)
NEGATIVISM ( 18 FDA reports)
OCULOGYRIC CRISIS ( 18 FDA reports)
OSTEOMYELITIS CHRONIC ( 18 FDA reports)
PERICARDITIS ( 18 FDA reports)
POTENTIATING DRUG INTERACTION ( 18 FDA reports)
PULMONARY INFARCTION ( 18 FDA reports)
PULMONARY RADIATION INJURY ( 18 FDA reports)
SPINAL CORD DISORDER ( 18 FDA reports)
TEMPORAL ARTERITIS ( 18 FDA reports)
VAGINAL DISCHARGE ( 18 FDA reports)
VENTRICULAR DYSFUNCTION ( 18 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 18 FDA reports)
VITAMIN B12 INCREASED ( 18 FDA reports)
TOOTH DISCOLOURATION ( 17 FDA reports)
UTERINE CANCER ( 17 FDA reports)
VAGINAL INFECTION ( 17 FDA reports)
VERTIGO POSITIONAL ( 17 FDA reports)
VITAMIN A DEFICIENCY ( 17 FDA reports)
VITREOUS DETACHMENT ( 17 FDA reports)
VITREOUS HAEMORRHAGE ( 17 FDA reports)
ANAL HAEMORRHAGE ( 17 FDA reports)
APPLICATION SITE PAIN ( 17 FDA reports)
ATROPHY ( 17 FDA reports)
BACTERIAL TEST POSITIVE ( 17 FDA reports)
BLOOD CULTURE POSITIVE ( 17 FDA reports)
BLOOD MAGNESIUM DECREASED ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 17 FDA reports)
BONE OPERATION ( 17 FDA reports)
BUNION ( 17 FDA reports)
CRANIAL NERVE DISORDER ( 17 FDA reports)
CYSTOCELE ( 17 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 17 FDA reports)
DIZZINESS POSTURAL ( 17 FDA reports)
ENDOMETRIOSIS ( 17 FDA reports)
EYE ALLERGY ( 17 FDA reports)
FLUID INTAKE REDUCED ( 17 FDA reports)
FOOD CRAVING ( 17 FDA reports)
GASTROINTESTINAL NECROSIS ( 17 FDA reports)
GRIMACING ( 17 FDA reports)
HEPATITIS CHOLESTATIC ( 17 FDA reports)
HEPATITIS TOXIC ( 17 FDA reports)
HIGH FREQUENCY ABLATION ( 17 FDA reports)
HYPERTHERMIA MALIGNANT ( 17 FDA reports)
INHIBITORY DRUG INTERACTION ( 17 FDA reports)
JAW FRACTURE ( 17 FDA reports)
LIGAMENT SPRAIN ( 17 FDA reports)
LIP DISCOLOURATION ( 17 FDA reports)
MALABSORPTION ( 17 FDA reports)
MEDICAL DEVICE COMPLICATION ( 17 FDA reports)
MONOPLEGIA ( 17 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 17 FDA reports)
NEUTROPENIC SEPSIS ( 17 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 17 FDA reports)
PATHOLOGICAL GAMBLING ( 17 FDA reports)
PERFORATION BILE DUCT ( 17 FDA reports)
PERFORMANCE STATUS DECREASED ( 17 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 17 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 17 FDA reports)
PROCTALGIA ( 17 FDA reports)
PROSTATE CANCER ( 17 FDA reports)
PROSTATOMEGALY ( 17 FDA reports)
PSORIATIC ARTHROPATHY ( 17 FDA reports)
PULMONARY THROMBOSIS ( 17 FDA reports)
SIALOADENITIS ( 17 FDA reports)
SMALL FOR DATES BABY ( 17 FDA reports)
SNEEZING ( 17 FDA reports)
ACUTE PSYCHOSIS ( 16 FDA reports)
ANOXIC ENCEPHALOPATHY ( 16 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
ARTHROPOD BITE ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
AUTISM ( 16 FDA reports)
BLOOD OSMOLARITY INCREASED ( 16 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 16 FDA reports)
BONE ATROPHY ( 16 FDA reports)
BRADYPNOEA ( 16 FDA reports)
BREAST ABSCESS ( 16 FDA reports)
CARBON DIOXIDE INCREASED ( 16 FDA reports)
CATHETERISATION CARDIAC ( 16 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 16 FDA reports)
COMPARTMENT SYNDROME ( 16 FDA reports)
DEVICE OCCLUSION ( 16 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 16 FDA reports)
DYSAESTHESIA ( 16 FDA reports)
ELECTRIC SHOCK ( 16 FDA reports)
GASTROINTESTINAL PAIN ( 16 FDA reports)
GLOSSITIS ( 16 FDA reports)
HAEMORRHAGIC STROKE ( 16 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 16 FDA reports)
HYPOPNOEA ( 16 FDA reports)
IMPATIENCE ( 16 FDA reports)
INFERTILITY FEMALE ( 16 FDA reports)
INJECTION SITE PRURITUS ( 16 FDA reports)
INTESTINAL PERFORATION ( 16 FDA reports)
INTRA-UTERINE DEATH ( 16 FDA reports)
LISTLESS ( 16 FDA reports)
LOGORRHOEA ( 16 FDA reports)
LOW TURNOVER OSTEOPATHY ( 16 FDA reports)
MEAN CELL VOLUME INCREASED ( 16 FDA reports)
MONOCYTE COUNT DECREASED ( 16 FDA reports)
MUSCULOSKELETAL DISORDER ( 16 FDA reports)
NASAL NEOPLASM ( 16 FDA reports)
NEUROLOGICAL SYMPTOM ( 16 FDA reports)
PERSONALITY DISORDER ( 16 FDA reports)
PHARYNGEAL ERYTHEMA ( 16 FDA reports)
PHOBIA ( 16 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 16 FDA reports)
PROCEDURAL PAIN ( 16 FDA reports)
QRS AXIS ABNORMAL ( 16 FDA reports)
RECTAL POLYP ( 16 FDA reports)
SEBORRHOEIC KERATOSIS ( 16 FDA reports)
SELF ESTEEM DECREASED ( 16 FDA reports)
SHOCK HAEMORRHAGIC ( 16 FDA reports)
SICCA SYNDROME ( 16 FDA reports)
SOMATIC DELUSION ( 16 FDA reports)
SPINAL CORD COMPRESSION ( 16 FDA reports)
SPUTUM CULTURE POSITIVE ( 16 FDA reports)
TONGUE CYST ( 16 FDA reports)
VENOUS OCCLUSION ( 16 FDA reports)
SUBACUTE ENDOCARDITIS ( 15 FDA reports)
TALIPES ( 15 FDA reports)
THYROID ADENOMA ( 15 FDA reports)
URINARY HESITATION ( 15 FDA reports)
VITAMIN C DEFICIENCY ( 15 FDA reports)
ACCOMMODATION DISORDER ( 15 FDA reports)
AGEUSIA ( 15 FDA reports)
ANAEMIA MACROCYTIC ( 15 FDA reports)
ANOREXIA NERVOSA ( 15 FDA reports)
APGAR SCORE LOW ( 15 FDA reports)
APPARENT DEATH ( 15 FDA reports)
BILIARY DYSKINESIA ( 15 FDA reports)
BLADDER OBSTRUCTION ( 15 FDA reports)
BLINDNESS UNILATERAL ( 15 FDA reports)
BLOOD URIC ACID INCREASED ( 15 FDA reports)
BONE GRAFT ( 15 FDA reports)
BREAST CANCER RECURRENT ( 15 FDA reports)
BREAST LUMP REMOVAL ( 15 FDA reports)
BRONCHOPLEURAL FISTULA ( 15 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 15 FDA reports)
BURNS THIRD DEGREE ( 15 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 15 FDA reports)
CHOREA ( 15 FDA reports)
CLOSTRIDIAL INFECTION ( 15 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 15 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 15 FDA reports)
DRUG RESISTANCE ( 15 FDA reports)
EAR DISCOMFORT ( 15 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
ENDOCRINE DISORDER ( 15 FDA reports)
GROIN ABSCESS ( 15 FDA reports)
GUN SHOT WOUND ( 15 FDA reports)
HAEMANGIOMA ( 15 FDA reports)
HAEMORRHAGIC DIATHESIS ( 15 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 15 FDA reports)
HEPATIC MASS ( 15 FDA reports)
HYDROPNEUMOTHORAX ( 15 FDA reports)
HYPERAMMONAEMIA ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
IMMOBILE ( 15 FDA reports)
INJURY CORNEAL ( 15 FDA reports)
INTESTINAL ISCHAEMIA ( 15 FDA reports)
INTRACARDIAC THROMBUS ( 15 FDA reports)
IRIS DISORDER ( 15 FDA reports)
LEFT ATRIAL DILATATION ( 15 FDA reports)
LUNG CONSOLIDATION ( 15 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 15 FDA reports)
MENINGITIS ( 15 FDA reports)
NEONATAL ASPHYXIA ( 15 FDA reports)
NONSPECIFIC REACTION ( 15 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 15 FDA reports)
OSTEOCHONDROSIS ( 15 FDA reports)
PCO2 DECREASED ( 15 FDA reports)
PINEAL GLAND CYST ( 15 FDA reports)
PNEUMONIA BACTERIAL ( 15 FDA reports)
PROSTATE CANCER METASTATIC ( 15 FDA reports)
PROTRUSION TONGUE ( 15 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 15 FDA reports)
RASH PUSTULAR ( 15 FDA reports)
RECTOCELE ( 15 FDA reports)
SENSATION OF PRESSURE ( 15 FDA reports)
SINUS ARRHYTHMIA ( 15 FDA reports)
SKIN HAEMORRHAGE ( 15 FDA reports)
SMOKER ( 15 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 14 FDA reports)
ACINETOBACTER INFECTION ( 14 FDA reports)
ACUTE PRERENAL FAILURE ( 14 FDA reports)
AZOTAEMIA ( 14 FDA reports)
BARRETT'S OESOPHAGUS ( 14 FDA reports)
BLADDER PROLAPSE ( 14 FDA reports)
BLOOD IRON INCREASED ( 14 FDA reports)
BONE MARROW OEDEMA ( 14 FDA reports)
BRAIN INJURY ( 14 FDA reports)
BREAST ENLARGEMENT ( 14 FDA reports)
BREATH SOUNDS ABNORMAL ( 14 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 14 FDA reports)
CARDIAC FLUTTER ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CEREBROSCLEROSIS ( 14 FDA reports)
DEAFNESS UNILATERAL ( 14 FDA reports)
DUODENAL ULCER ( 14 FDA reports)
DYSPHASIA ( 14 FDA reports)
EAR INJURY ( 14 FDA reports)
EARLY MORNING AWAKENING ( 14 FDA reports)
ENCEPHALITIS ( 14 FDA reports)
FEEDING DISORDER NEONATAL ( 14 FDA reports)
FOETAL GROWTH RETARDATION ( 14 FDA reports)
FOLATE DEFICIENCY ( 14 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 14 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 14 FDA reports)
GRAFT ISCHAEMIA ( 14 FDA reports)
HEPATITIS FULMINANT ( 14 FDA reports)
HYPOREFLEXIA ( 14 FDA reports)
HYPOSPADIAS ( 14 FDA reports)
HYPOVOLAEMIC SHOCK ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 14 FDA reports)
LIPOMA ( 14 FDA reports)
LIVEDO RETICULARIS ( 14 FDA reports)
LUNG ABSCESS ( 14 FDA reports)
MALIGNANT MELANOMA IN SITU ( 14 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 14 FDA reports)
MEDICAL DEVICE REMOVAL ( 14 FDA reports)
MUCOSAL ULCERATION ( 14 FDA reports)
MYOCARDIAL RUPTURE ( 14 FDA reports)
NECK INJURY ( 14 FDA reports)
NEOPLASM PROGRESSION ( 14 FDA reports)
ONYCHOMYCOSIS ( 14 FDA reports)
PO2 INCREASED ( 14 FDA reports)
POSTNASAL DRIP ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
RENAL MASS ( 14 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 14 FDA reports)
SKIN GRAFT ( 14 FDA reports)
SKIN REACTION ( 14 FDA reports)
SKULL FRACTURE ( 14 FDA reports)
SOCIAL FEAR ( 14 FDA reports)
SOFT TISSUE INFECTION ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 14 FDA reports)
SUNBURN ( 14 FDA reports)
THORACOTOMY ( 14 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 14 FDA reports)
TONIC CONVULSION ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 14 FDA reports)
VERTEBRAL WEDGING ( 14 FDA reports)
STRESS INCONTINENCE ( 13 FDA reports)
TENOSYNOVITIS ( 13 FDA reports)
TONGUE DISCOLOURATION ( 13 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
UTERINE HAEMORRHAGE ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
ABNORMAL FAECES ( 13 FDA reports)
ALKALOSIS ( 13 FDA reports)
APPETITE DISORDER ( 13 FDA reports)
APPLICATION SITE REACTION ( 13 FDA reports)
BLOOD CHLORIDE INCREASED ( 13 FDA reports)
BLOOD CREATINE INCREASED ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 13 FDA reports)
BLOOD URINE ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 13 FDA reports)
BREAST CALCIFICATIONS ( 13 FDA reports)
BREAST SWELLING ( 13 FDA reports)
CAROTID ARTERY DISEASE ( 13 FDA reports)
CATHETER REMOVAL ( 13 FDA reports)
CERUMEN IMPACTION ( 13 FDA reports)
CLONIC CONVULSION ( 13 FDA reports)
COLITIS ISCHAEMIC ( 13 FDA reports)
DENTAL PROSTHESIS USER ( 13 FDA reports)
DISSEMINATED TUBERCULOSIS ( 13 FDA reports)
DRUG DIVERSION ( 13 FDA reports)
DRUG TOLERANCE INCREASED ( 13 FDA reports)
ELEVATED MOOD ( 13 FDA reports)
EMBOLISM ( 13 FDA reports)
FACE INJURY ( 13 FDA reports)
FULL BLOOD COUNT DECREASED ( 13 FDA reports)
GASTROINTESTINAL INFECTION ( 13 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 13 FDA reports)
HAEMOGLOBIN INCREASED ( 13 FDA reports)
HEPATIC PAIN ( 13 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 13 FDA reports)
HYPERCORTICOIDISM ( 13 FDA reports)
HYPERKERATOSIS ( 13 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 13 FDA reports)
IMPAIRED SELF-CARE ( 13 FDA reports)
INTERVERTEBRAL DISCITIS ( 13 FDA reports)
ISCHAEMIC STROKE ( 13 FDA reports)
KIDNEY MALROTATION ( 13 FDA reports)
KLEBSIELLA INFECTION ( 13 FDA reports)
LIGAMENT RUPTURE ( 13 FDA reports)
MALIGNANT MELANOMA ( 13 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 13 FDA reports)
MOUTH HAEMORRHAGE ( 13 FDA reports)
MUSCLE CRAMP ( 13 FDA reports)
ORAL INFECTION ( 13 FDA reports)
ORAL INTAKE REDUCED ( 13 FDA reports)
OSTEOMALACIA ( 13 FDA reports)
OTITIS MEDIA ( 13 FDA reports)
PANCREATITIS CHRONIC ( 13 FDA reports)
PERICARDIAL HAEMORRHAGE ( 13 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 13 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 13 FDA reports)
POLYMYALGIA RHEUMATICA ( 13 FDA reports)
POSTURING ( 13 FDA reports)
PRIAPISM ( 13 FDA reports)
PROTEIN TOTAL INCREASED ( 13 FDA reports)
PROTEINURIA ( 13 FDA reports)
PULMONARY ARTERY DILATATION ( 13 FDA reports)
PYELONEPHRITIS ACUTE ( 13 FDA reports)
RASH VESICULAR ( 13 FDA reports)
SINUS POLYP DEGENERATION ( 13 FDA reports)
SKIN HYPERPIGMENTATION ( 13 FDA reports)
SLEEP WALKING ( 13 FDA reports)
ABORTION INDUCED ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
AORTIC CALCIFICATION ( 12 FDA reports)
APPENDICECTOMY ( 12 FDA reports)
ASTIGMATISM ( 12 FDA reports)
BRAIN NEOPLASM ( 12 FDA reports)
BREAST TENDERNESS ( 12 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 12 FDA reports)
CARDIAC OPERATION ( 12 FDA reports)
CARDIAC PACEMAKER INSERTION ( 12 FDA reports)
CATHETER PLACEMENT ( 12 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 12 FDA reports)
CHEST WALL PAIN ( 12 FDA reports)
CHOLECYSTITIS INFECTIVE ( 12 FDA reports)
COELIAC DISEASE ( 12 FDA reports)
CORONARY ARTERY BYPASS ( 12 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 12 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 12 FDA reports)
DEPRESSION SUICIDAL ( 12 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 12 FDA reports)
DYSGRAPHIA ( 12 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 12 FDA reports)
ENDOTRACHEAL INTUBATION ( 12 FDA reports)
FACIAL SPASM ( 12 FDA reports)
FEBRILE CONVULSION ( 12 FDA reports)
FISTULA DISCHARGE ( 12 FDA reports)
FURUNCLE ( 12 FDA reports)
GASTRIC DILATATION ( 12 FDA reports)
GASTROENTERITIS SALMONELLA ( 12 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 12 FDA reports)
GASTROINTESTINAL SURGERY ( 12 FDA reports)
GENERAL SYMPTOM ( 12 FDA reports)
GRIEF REACTION ( 12 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 12 FDA reports)
HANGOVER ( 12 FDA reports)
HERNIA REPAIR ( 12 FDA reports)
IATROGENIC INJURY ( 12 FDA reports)
INJECTION SITE DISCOLOURATION ( 12 FDA reports)
INJECTION SITE INFLAMMATION ( 12 FDA reports)
INJECTION SITE ULCER ( 12 FDA reports)
INTESTINAL HAEMORRHAGE ( 12 FDA reports)
INTRAOCULAR LENS IMPLANT ( 12 FDA reports)
JOINT CONTRACTURE ( 12 FDA reports)
LACUNAR INFARCTION ( 12 FDA reports)
LIBIDO INCREASED ( 12 FDA reports)
LOSS OF CONTROL OF LEGS ( 12 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 12 FDA reports)
MARITAL PROBLEM ( 12 FDA reports)
MASTITIS ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MYOCARDIAL FIBROSIS ( 12 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 12 FDA reports)
OPEN WOUND ( 12 FDA reports)
OROPHARYNGEAL BLISTERING ( 12 FDA reports)
OTITIS EXTERNA ( 12 FDA reports)
OVERWEIGHT ( 12 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
POST PROCEDURAL BILE LEAK ( 12 FDA reports)
PROCEDURAL HYPOTENSION ( 12 FDA reports)
PROTEIN URINE PRESENT ( 12 FDA reports)
PULMONARY TOXICITY ( 12 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 12 FDA reports)
RESPIRATORY TRACT CONGESTION ( 12 FDA reports)
ROSACEA ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SIMPLE PARTIAL SEIZURES ( 12 FDA reports)
SKIN NEOPLASM EXCISION ( 12 FDA reports)
SKIN PAPILLOMA ( 12 FDA reports)
SLEEP TERROR ( 12 FDA reports)
SOLILOQUY ( 12 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 12 FDA reports)
TACHYPHRENIA ( 12 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 12 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 12 FDA reports)
VITAMIN B12 DEFICIENCY ( 12 FDA reports)
VOCAL CORD PARALYSIS ( 12 FDA reports)
WOUND SECRETION ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
STARING ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 11 FDA reports)
THERAPY REGIMEN CHANGED ( 11 FDA reports)
URETERIC OBSTRUCTION ( 11 FDA reports)
VERTEBROPLASTY ( 11 FDA reports)
VESTIBULAR DISORDER ( 11 FDA reports)
WALKING DISABILITY ( 11 FDA reports)
ABDOMINAL ADHESIONS ( 11 FDA reports)
ANKYLOSING SPONDYLITIS ( 11 FDA reports)
ANOGENITAL WARTS ( 11 FDA reports)
ANORGASMIA ( 11 FDA reports)
APPLICATION SITE PRURITUS ( 11 FDA reports)
ASPIRATION BRONCHIAL ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BIPOLAR I DISORDER ( 11 FDA reports)
BLADDER CANCER ( 11 FDA reports)
BLOOD BLISTER ( 11 FDA reports)
BLOOD CALCIUM INCREASED ( 11 FDA reports)
BONE MARROW TOXICITY ( 11 FDA reports)
BRADYARRHYTHMIA ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BREAST DISCHARGE ( 11 FDA reports)
BRONCHITIS ACUTE ( 11 FDA reports)
CARDIAC ANEURYSM ( 11 FDA reports)
CARDIAC FAILURE ACUTE ( 11 FDA reports)
CHOREOATHETOSIS ( 11 FDA reports)
CLEFT LIP ( 11 FDA reports)
COLLAPSE OF LUNG ( 11 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 11 FDA reports)
CONCUSSION ( 11 FDA reports)
CONGENITAL ANOMALY ( 11 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 11 FDA reports)
DAYDREAMING ( 11 FDA reports)
DETOXIFICATION ( 11 FDA reports)
DEVICE BREAKAGE ( 11 FDA reports)
DILATATION ATRIAL ( 11 FDA reports)
DYSPRAXIA ( 11 FDA reports)
ENDOCARDITIS ( 11 FDA reports)
ESSENTIAL HYPERTENSION ( 11 FDA reports)
FALLOT'S TETRALOGY ( 11 FDA reports)
FINGER DEFORMITY ( 11 FDA reports)
FRACTURE NONUNION ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
GAZE PALSY ( 11 FDA reports)
GRIP STRENGTH DECREASED ( 11 FDA reports)
HEPATOCELLULAR INJURY ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYPERURICAEMIA ( 11 FDA reports)
IMPETIGO ( 11 FDA reports)
INAPPROPRIATE AFFECT ( 11 FDA reports)
INGROWING NAIL ( 11 FDA reports)
INJECTION SITE IRRITATION ( 11 FDA reports)
INTESTINAL POLYP ( 11 FDA reports)
INTESTINAL ULCER ( 11 FDA reports)
INTRACRANIAL HYPOTENSION ( 11 FDA reports)
JOINT LOCK ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 11 FDA reports)
LEARNING DISORDER ( 11 FDA reports)
LIGAMENT OPERATION ( 11 FDA reports)
LOCALISED OEDEMA ( 11 FDA reports)
MARCHIAFAVA-BIGNAMI DISEASE ( 11 FDA reports)
MICROCYTIC ANAEMIA ( 11 FDA reports)
MUSCLE CONTRACTURE ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
NEURODERMATITIS ( 11 FDA reports)
NICOTINE DEPENDENCE ( 11 FDA reports)
NOSOCOMIAL INFECTION ( 11 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 11 FDA reports)
OBSESSIVE THOUGHTS ( 11 FDA reports)
OESOPHAGEAL PAIN ( 11 FDA reports)
PAIN EXACERBATED ( 11 FDA reports)
PAPULE ( 11 FDA reports)
PENILE OEDEMA ( 11 FDA reports)
PERIODONTITIS ( 11 FDA reports)
PERIORBITAL HAEMATOMA ( 11 FDA reports)
PHLEBITIS ( 11 FDA reports)
PITTING OEDEMA ( 11 FDA reports)
PLEURAL DISORDER ( 11 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 11 FDA reports)
PROSTATIC DISORDER ( 11 FDA reports)
PROSTATITIS ( 11 FDA reports)
PULSE ABNORMAL ( 11 FDA reports)
READING DISORDER ( 11 FDA reports)
REFRACTION DISORDER ( 11 FDA reports)
REGRESSIVE BEHAVIOUR ( 11 FDA reports)
RETINAL HAEMORRHAGE ( 11 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SKIN FISSURES ( 11 FDA reports)
SOMATOFORM DISORDER ( 11 FDA reports)
ABDOMINAL HERNIA ( 10 FDA reports)
ABORTION ( 10 FDA reports)
ACTINOMYCOSIS ( 10 FDA reports)
AGITATION NEONATAL ( 10 FDA reports)
ANOSMIA ( 10 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
AORTIC ANEURYSM RUPTURE ( 10 FDA reports)
ARTERIOSPASM CORONARY ( 10 FDA reports)
ATROPHIC VULVOVAGINITIS ( 10 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 10 FDA reports)
BILE DUCT OBSTRUCTION ( 10 FDA reports)
BLADDER CATHETERISATION ( 10 FDA reports)
BLADDER DILATATION ( 10 FDA reports)
BLEPHARITIS ( 10 FDA reports)
BLUNTED AFFECT ( 10 FDA reports)
BREAKTHROUGH PAIN ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CARDIAC ENZYMES INCREASED ( 10 FDA reports)
CARDIAC HYPERTROPHY ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CEREBRAL DISORDER ( 10 FDA reports)
CHRONIC FATIGUE SYNDROME ( 10 FDA reports)
COLON POLYPECTOMY ( 10 FDA reports)
CONGENITAL HIP DEFORMITY ( 10 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 10 FDA reports)
DEATH OF RELATIVE ( 10 FDA reports)
DENTAL OPERATION ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DEVICE LEAKAGE ( 10 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 10 FDA reports)
DRY THROAT ( 10 FDA reports)
EJACULATION FAILURE ( 10 FDA reports)
ENERGY INCREASED ( 10 FDA reports)
EPIDERMOLYSIS ( 10 FDA reports)
EPIGASTRIC DISCOMFORT ( 10 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 10 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 10 FDA reports)
EXANTHEM ( 10 FDA reports)
EYE PRURITUS ( 10 FDA reports)
FACIAL BONES FRACTURE ( 10 FDA reports)
FEAR OF DEATH ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
GASTROPTOSIS ( 10 FDA reports)
GINGIVAL ATROPHY ( 10 FDA reports)
HAIR COLOUR CHANGES ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HILAR LYMPHADENOPATHY ( 10 FDA reports)
HODGKIN'S DISEASE ( 10 FDA reports)
HYPOTONIA NEONATAL ( 10 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 10 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 10 FDA reports)
LEUKAEMIA ( 10 FDA reports)
LEUKOENCEPHALOPATHY ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
LONG QT SYNDROME ( 10 FDA reports)
LYMPHOPENIA ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
MASTECTOMY ( 10 FDA reports)
MEDICATION RESIDUE ( 10 FDA reports)
MENTAL RETARDATION ( 10 FDA reports)
METASTASES TO PERITONEUM ( 10 FDA reports)
METATARSUS PRIMUS VARUS ( 10 FDA reports)
MICTURITION DISORDER ( 10 FDA reports)
MITRAL VALVE DISEASE ( 10 FDA reports)
MORAXELLA INFECTION ( 10 FDA reports)
NEUROGENIC SHOCK ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
OLIGOHYDRAMNIOS ( 10 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 10 FDA reports)
PARATHYROID TUMOUR BENIGN ( 10 FDA reports)
PAROTITIS ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PCO2 INCREASED ( 10 FDA reports)
PERIVASCULAR DERMATITIS ( 10 FDA reports)
PIERRE ROBIN SYNDROME ( 10 FDA reports)
PNEUMONIA HAEMOPHILUS ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 10 FDA reports)
POLYTRAUMATISM ( 10 FDA reports)
PSYCHOMOTOR RETARDATION ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
PULMONARY ARTERY STENOSIS ( 10 FDA reports)
PULMONARY MASS ( 10 FDA reports)
PYURIA ( 10 FDA reports)
RADIOTHERAPY ( 10 FDA reports)
RECTAL FISSURE ( 10 FDA reports)
REFLEXES ABNORMAL ( 10 FDA reports)
RENAL CANCER ( 10 FDA reports)
RESPIRATION ABNORMAL ( 10 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
RIGHT VENTRICULAR FAILURE ( 10 FDA reports)
SKIN EROSION ( 10 FDA reports)
SKIN INJURY ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
SPUTUM RETENTION ( 10 FDA reports)
STEREOTYPY ( 10 FDA reports)
SUFFOCATION FEELING ( 10 FDA reports)
SWEAT GLAND DISORDER ( 10 FDA reports)
SYNDACTYLY ( 10 FDA reports)
SYNOVITIS ( 10 FDA reports)
TIC ( 10 FDA reports)
TONGUE PARALYSIS ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 10 FDA reports)
UNDERDOSE ( 10 FDA reports)
VASCULAR PSEUDOANEURYSM ( 10 FDA reports)
VENTRICULAR ARRHYTHMIA ( 10 FDA reports)
WEIGHT FLUCTUATION ( 10 FDA reports)
SUDDEN ONSET OF SLEEP ( 9 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 9 FDA reports)
TONGUE INJURY ( 9 FDA reports)
TROPONIN I INCREASED ( 9 FDA reports)
URETERAL STENT INSERTION ( 9 FDA reports)
URINE COLOUR ABNORMAL ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 9 FDA reports)
ABDOMINAL MASS ( 9 FDA reports)
ACCIDENT AT WORK ( 9 FDA reports)
ACTIVATION SYNDROME ( 9 FDA reports)
ALLODYNIA ( 9 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 9 FDA reports)
ANAL ABSCESS ( 9 FDA reports)
ANDROGENS ABNORMAL ( 9 FDA reports)
ANORECTAL DISCOMFORT ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC VALVE SCLEROSIS ( 9 FDA reports)
APPLICATION SITE BURN ( 9 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 9 FDA reports)
BLOOD IRON DECREASED ( 9 FDA reports)
BONE SWELLING ( 9 FDA reports)
BRAIN STEM INFARCTION ( 9 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 9 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
CARTILAGE INJURY ( 9 FDA reports)
CERVICOBRACHIAL SYNDROME ( 9 FDA reports)
CHAPPED LIPS ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CNS VENTRICULITIS ( 9 FDA reports)
CONDUCTION DISORDER ( 9 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 9 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 9 FDA reports)
CORNEAL DYSTROPHY ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CSF TEST ABNORMAL ( 9 FDA reports)
CYCLOTHYMIC DISORDER ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DIABETIC RETINOPATHY ( 9 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 9 FDA reports)
DRUG CLEARANCE DECREASED ( 9 FDA reports)
EAR DISORDER ( 9 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 9 FDA reports)
FAT NECROSIS ( 9 FDA reports)
FEMALE STERILISATION ( 9 FDA reports)
FEMORAL NECK FRACTURE ( 9 FDA reports)
FOREIGN BODY ASPIRATION ( 9 FDA reports)
GASTRIC CANCER ( 9 FDA reports)
GASTROINTESTINAL CARCINOMA ( 9 FDA reports)
GASTROINTESTINAL PERFORATION ( 9 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HEPATIC FIBROSIS ( 9 FDA reports)
HEPATORENAL FAILURE ( 9 FDA reports)
HERPES SIMPLEX ( 9 FDA reports)
HORDEOLUM ( 9 FDA reports)
HYPERCHLORHYDRIA ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 9 FDA reports)
INJECTION SITE ABSCESS ( 9 FDA reports)
INJECTION SITE MASS ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
INTESTINAL DILATATION ( 9 FDA reports)
ISCHAEMIC HEPATITIS ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
KETONURIA ( 9 FDA reports)
LEUKOPLAKIA ORAL ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
LUNG INJURY ( 9 FDA reports)
METASTASES TO SKIN ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MYOPIA ( 9 FDA reports)
NASAL SEPTUM DEVIATION ( 9 FDA reports)
NASAL SINUS CANCER ( 9 FDA reports)
NEPHRITIS INTERSTITIAL ( 9 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 9 FDA reports)
OPEN REDUCTION OF FRACTURE ( 9 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 9 FDA reports)
ORGANISING PNEUMONIA ( 9 FDA reports)
OSMOLAR GAP ABNORMAL ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
PARTNER STRESS ( 9 FDA reports)
PATELLA FRACTURE ( 9 FDA reports)
PERIORBITAL OEDEMA ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
PLACENTAL INSUFFICIENCY ( 9 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 9 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 9 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 9 FDA reports)
RECTAL ABSCESS ( 9 FDA reports)
RETINAL DETACHMENT ( 9 FDA reports)
RETROPERITONEAL HAEMATOMA ( 9 FDA reports)
SENSATION OF FOREIGN BODY ( 9 FDA reports)
SINUS RHYTHM ( 9 FDA reports)
SKIN SWELLING ( 9 FDA reports)
SLEEP PARALYSIS ( 9 FDA reports)
SOMNOLENCE NEONATAL ( 9 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 8 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
ANORECTAL OPERATION ( 8 FDA reports)
AORTIC STENOSIS ( 8 FDA reports)
ASEPTIC NECROSIS BONE ( 8 FDA reports)
BILIARY COLIC ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 8 FDA reports)
BONE MARROW DISORDER ( 8 FDA reports)
BONE NEOPLASM MALIGNANT ( 8 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BRONCHITIS CHRONIC ( 8 FDA reports)
CANCER PAIN ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CARDIAC OUTPUT DECREASED ( 8 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CLONUS ( 8 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 8 FDA reports)
COMPULSIONS ( 8 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 8 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
DELUSION OF REPLACEMENT ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DIABETIC ULCER ( 8 FDA reports)
DRUG DETOXIFICATION ( 8 FDA reports)
DYSMENORRHOEA ( 8 FDA reports)
DYSSOMNIA ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
ENCEPHALITIS HERPES ( 8 FDA reports)
ENTERITIS ( 8 FDA reports)
EOSINOPHIL COUNT DECREASED ( 8 FDA reports)
EXCESSIVE MASTURBATION ( 8 FDA reports)
EXFOLIATIVE RASH ( 8 FDA reports)
EYE INFLAMMATION ( 8 FDA reports)
EYELID DISORDER ( 8 FDA reports)
FAECES HARD ( 8 FDA reports)
FEAR OF FALLING ( 8 FDA reports)
FEELINGS OF WORTHLESSNESS ( 8 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 8 FDA reports)
FINE MOTOR DELAY ( 8 FDA reports)
FLIGHT OF IDEAS ( 8 FDA reports)
FOAMING AT MOUTH ( 8 FDA reports)
FOETAL ALCOHOL SYNDROME ( 8 FDA reports)
FOETAL HYPOKINESIA ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
GENITAL EROSION ( 8 FDA reports)
GLOSSOPTOSIS ( 8 FDA reports)
GRANULOCYTOSIS ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEART INJURY ( 8 FDA reports)
HEAT EXHAUSTION ( 8 FDA reports)
HERPES VIRUS INFECTION ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPOPHOSPHATAEMIA ( 8 FDA reports)
IMPRISONMENT ( 8 FDA reports)
INFARCTION ( 8 FDA reports)
INJECTION SITE INDURATION ( 8 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 8 FDA reports)
JOINT STABILISATION ( 8 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 8 FDA reports)
LUNG OPERATION ( 8 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 8 FDA reports)
MUSCLE FATIGUE ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME ( 8 FDA reports)
NAIL DISORDER ( 8 FDA reports)
NEURITIS ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
ODYNOPHAGIA ( 8 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 8 FDA reports)
OESOPHAGEAL DISORDER ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
ORAL BACTERIAL INFECTION ( 8 FDA reports)
PANCREATIC ATROPHY ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PARADOXICAL DRUG REACTION ( 8 FDA reports)
PEAU D'ORANGE ( 8 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 8 FDA reports)
PORPHYRIA ACUTE ( 8 FDA reports)
POST PROCEDURAL PAIN ( 8 FDA reports)
POSTOPERATIVE INFECTION ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PRODUCT FORMULATION ISSUE ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
PULMONARY CAVITATION ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 8 FDA reports)
RECTAL PROLAPSE ( 8 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 8 FDA reports)
REGURGITATION ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SPINAL COLUMN INJURY ( 8 FDA reports)
SPINAL CORPECTOMY ( 8 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 8 FDA reports)
STENT PLACEMENT ( 8 FDA reports)
STRESS SYMPTOMS ( 8 FDA reports)
TENDON PAIN ( 8 FDA reports)
THROMBOCYTHAEMIA ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
TONGUE SPASM ( 8 FDA reports)
TROPONIN T INCREASED ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
URINARY TRACT DISORDER ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 8 FDA reports)
WOUND COMPLICATION ( 8 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
TARSAL TUNNEL SYNDROME ( 7 FDA reports)
TONGUE OEDEMA ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
TRICHOTILLOMANIA ( 7 FDA reports)
URINE KETONE BODY PRESENT ( 7 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 7 FDA reports)
VAGINITIS ATROPHIC ( 7 FDA reports)
VASCULAR GRAFT OCCLUSION ( 7 FDA reports)
VASCULAR OCCLUSION ( 7 FDA reports)
VASCULAR STENOSIS ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
VISCERAL CONGESTION ( 7 FDA reports)
WEIGHT LOSS POOR ( 7 FDA reports)
X-RAY ABNORMAL ( 7 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACTINIC KERATOSIS ( 7 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 7 FDA reports)
AORTIC VALVE DISEASE ( 7 FDA reports)
APLASIA PURE RED CELL ( 7 FDA reports)
APPENDICITIS PERFORATED ( 7 FDA reports)
APRAXIA ( 7 FDA reports)
APTYALISM ( 7 FDA reports)
ARTHROSCOPIC SURGERY ( 7 FDA reports)
ATONIC SEIZURES ( 7 FDA reports)
AURICULAR SWELLING ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
BASOPHIL COUNT DECREASED ( 7 FDA reports)
BEREAVEMENT REACTION ( 7 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 7 FDA reports)
BLADDER DYSFUNCTION ( 7 FDA reports)
BLOOD CORTISOL INCREASED ( 7 FDA reports)
BLOOD COUNT ABNORMAL ( 7 FDA reports)
BLOOD OSMOLARITY DECREASED ( 7 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 7 FDA reports)
BRAIN DAMAGE ( 7 FDA reports)
BREAST CANCER STAGE III ( 7 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 7 FDA reports)
BUTTOCK PAIN ( 7 FDA reports)
CATHETER SEPSIS ( 7 FDA reports)
CELL MARKER INCREASED ( 7 FDA reports)
CERVICAL MYELOPATHY ( 7 FDA reports)
CHEMICAL POISONING ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 7 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 7 FDA reports)
CLUSTER HEADACHE ( 7 FDA reports)
COARCTATION OF THE AORTA ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
CONGENITAL EYE DISORDER ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
DERMATITIS BULLOUS ( 7 FDA reports)
DIABETIC FOOT ( 7 FDA reports)
DIARRHOEA INFECTIOUS ( 7 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 7 FDA reports)
DIPLEGIA ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
EJACULATION DISORDER ( 7 FDA reports)
EMBOLIC STROKE ( 7 FDA reports)
ENCEPHALITIS VIRAL ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
EYE ROLLING ( 7 FDA reports)
FEELING GUILTY ( 7 FDA reports)
FOOD INTERACTION ( 7 FDA reports)
FOOD INTOLERANCE ( 7 FDA reports)
FOOD POISONING ( 7 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 7 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 7 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 7 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 7 FDA reports)
GLIOSIS ( 7 FDA reports)
HAIR GROWTH ABNORMAL ( 7 FDA reports)
HEAT STROKE ( 7 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 7 FDA reports)
HISTOLOGY ABNORMAL ( 7 FDA reports)
HYPERTONIA NEONATAL ( 7 FDA reports)
HYPERVIGILANCE ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
IMPLANT SITE PAIN ( 7 FDA reports)
INJECTION SITE THROMBOSIS ( 7 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 7 FDA reports)
INTUBATION ( 7 FDA reports)
KLEBSIELLA BACTERAEMIA ( 7 FDA reports)
LABORATORY TEST INTERFERENCE ( 7 FDA reports)
LARYNGEAL INFLAMMATION ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 7 FDA reports)
LUNG ADENOCARCINOMA ( 7 FDA reports)
MACULOPATHY ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
MENINGIOMA ( 7 FDA reports)
MENSTRUATION DELAYED ( 7 FDA reports)
MICROTIA ( 7 FDA reports)
MONONEUROPATHY MULTIPLEX ( 7 FDA reports)
MOTOR NEURONE DISEASE ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MYELOPATHY ( 7 FDA reports)
NEEDLE TRACK MARKS ( 7 FDA reports)
NEURODEGENERATIVE DISORDER ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER ( 7 FDA reports)
OCCULT BLOOD ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
ORAL MUCOSA EROSION ( 7 FDA reports)
ORAL TORUS ( 7 FDA reports)
ORGAN FAILURE ( 7 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
OTORRHOEA ( 7 FDA reports)
OVARIAN ATROPHY ( 7 FDA reports)
OXYGEN SATURATION ABNORMAL ( 7 FDA reports)
PARATHYROID DISORDER ( 7 FDA reports)
PELVIC ADHESIONS ( 7 FDA reports)
PELVIC MASS ( 7 FDA reports)
PELVIC PROLAPSE ( 7 FDA reports)
PHARYNGEAL ULCERATION ( 7 FDA reports)
PNEUMONIA VIRAL ( 7 FDA reports)
PORPHYRIA ( 7 FDA reports)
POVERTY OF SPEECH ( 7 FDA reports)
PREMATURE DELIVERY ( 7 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PSYCHOTIC BEHAVIOUR ( 7 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 7 FDA reports)
PURPURA SENILE ( 7 FDA reports)
QUADRIPLEGIA ( 7 FDA reports)
RADIATION SKIN INJURY ( 7 FDA reports)
RENAL HAEMORRHAGE ( 7 FDA reports)
RENAL INFARCT ( 7 FDA reports)
RESPIRATORY ALKALOSIS ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
RHEUMATIC HEART DISEASE ( 7 FDA reports)
SKIN TOXICITY ( 7 FDA reports)
SMEAR CERVIX ABNORMAL ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
SPONDYLOLYSIS ( 7 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 7 FDA reports)
ABDOMINAL HAEMATOMA ( 6 FDA reports)
ACARODERMATITIS ( 6 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ADENOMA BENIGN ( 6 FDA reports)
ADRENAL ADENOMA ( 6 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
ALCOHOLIC LIVER DISEASE ( 6 FDA reports)
ALVEOLOPLASTY ( 6 FDA reports)
AMIMIA ( 6 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 6 FDA reports)
ANAL FISTULA ( 6 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 6 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
ARTHROPOD STING ( 6 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
AUTISM SPECTRUM DISORDER ( 6 FDA reports)
BED REST ( 6 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 6 FDA reports)
BLADDER SPASM ( 6 FDA reports)
BLOOD ALBUMIN INCREASED ( 6 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 6 FDA reports)
BLOOD ETHANOL INCREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 6 FDA reports)
BONE CYST ( 6 FDA reports)
BONE FRAGMENTATION ( 6 FDA reports)
BRAIN MIDLINE SHIFT ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
BRUGADA SYNDROME ( 6 FDA reports)
BUNION OPERATION ( 6 FDA reports)
CALCULUS BLADDER ( 6 FDA reports)
CARDIAC INDEX INCREASED ( 6 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 6 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
CATHETER RELATED INFECTION ( 6 FDA reports)
CEREBELLAR INFARCTION ( 6 FDA reports)
CERVICITIS ( 6 FDA reports)
CERVIX INFLAMMATION ( 6 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 6 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 6 FDA reports)
COLD COMPRESS THERAPY ( 6 FDA reports)
COLECTOMY ( 6 FDA reports)
COLOBOMA ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
CONGENITAL VISUAL ACUITY REDUCED ( 6 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 6 FDA reports)
CORNEAL REFLEX DECREASED ( 6 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 6 FDA reports)
CULTURE POSITIVE ( 6 FDA reports)
CULTURE URINE POSITIVE ( 6 FDA reports)
DANDRUFF ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DELUSIONAL PERCEPTION ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DIABETIC GASTROPARESIS ( 6 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 6 FDA reports)
DRUG INTERACTION POTENTIATION ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
DRUG SCREEN NEGATIVE ( 6 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 6 FDA reports)
DYSENTERY ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSPAREUNIA ( 6 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
EXOPHTHALMOS ( 6 FDA reports)
EXTRASKELETAL OSSIFICATION ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FEELING HOT AND COLD ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 6 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 6 FDA reports)
GALLBLADDER INJURY ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GAUCHER'S DISEASE ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAIR TEXTURE ABNORMAL ( 6 FDA reports)
HEART SOUNDS ABNORMAL ( 6 FDA reports)
HEPATITIS A ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
HYPERTENSIVE EMERGENCY ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
ILLOGICAL THINKING ( 6 FDA reports)
IMPLANT SITE EFFUSION ( 6 FDA reports)
INDIFFERENCE ( 6 FDA reports)
INFANTILE APNOEIC ATTACK ( 6 FDA reports)
INJECTION SITE INFECTION ( 6 FDA reports)
INJECTION SITE NODULE ( 6 FDA reports)
INJECTION SITE SCAR ( 6 FDA reports)
INTERCOSTAL NEURALGIA ( 6 FDA reports)
INTERNAL HERNIA ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
KIDNEY ENLARGEMENT ( 6 FDA reports)
KOEBNER PHENOMENON ( 6 FDA reports)
LARYNGEAL STENOSIS ( 6 FDA reports)
LEARNING DISABILITY ( 6 FDA reports)
LEUKAEMIC INFILTRATION RENAL ( 6 FDA reports)
LIBIDO DISORDER ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LIMB OPERATION ( 6 FDA reports)
LINEAR IGA DISEASE ( 6 FDA reports)
LIP DISORDER ( 6 FDA reports)
LUMBAR HERNIA ( 6 FDA reports)
LYMPHANGIOMA ( 6 FDA reports)
MAMMARY DUCT ECTASIA ( 6 FDA reports)
MAMMOGRAM ABNORMAL ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METAPLASIA ( 6 FDA reports)
MOANING ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MYCOPLASMA INFECTION ( 6 FDA reports)
MYCOSIS FUNGOIDES ( 6 FDA reports)
MYELITIS ( 6 FDA reports)
MYELITIS TRANSVERSE ( 6 FDA reports)
MYOCLONIC EPILEPSY ( 6 FDA reports)
MYOGLOBIN URINE PRESENT ( 6 FDA reports)
NARCOLEPSY ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NECROTISING COLITIS ( 6 FDA reports)
NEONATAL COMPLICATIONS OF SUBSTANCE ABUSE ( 6 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 6 FDA reports)
NEONATAL TACHYPNOEA ( 6 FDA reports)
NOCTURNAL DYSPNOEA ( 6 FDA reports)
OCULAR NEOPLASM ( 6 FDA reports)
OESOPHAGEAL NEOPLASM ( 6 FDA reports)
OOPHORECTOMY ( 6 FDA reports)
ORAL FUNGAL INFECTION ( 6 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 6 FDA reports)
OROPHARYNGEAL SPASM ( 6 FDA reports)
OROPHARYNGEAL SWELLING ( 6 FDA reports)
PANCREATIC CYST ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PATHOGEN RESISTANCE ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PERITONEAL DIALYSIS ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PNEUMONIA MYCOPLASMAL ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POOR PERIPHERAL CIRCULATION ( 6 FDA reports)
PORIOMANIA ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
POST PROCEDURAL INFECTION ( 6 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 6 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
RENAL TUBULAR DISORDER ( 6 FDA reports)
RETINAL VEIN OCCLUSION ( 6 FDA reports)
RHINITIS SEASONAL ( 6 FDA reports)
SALPINGO-OOPHORECTOMY ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
SECRETION DISCHARGE ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN ODOUR ABNORMAL ( 6 FDA reports)
SOMATISATION DISORDER ( 6 FDA reports)
SPERMATOGENESIS ABNORMAL ( 6 FDA reports)
SPONDYLOSIS ( 6 FDA reports)
STENOTROPHOMONAS INFECTION ( 6 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 6 FDA reports)
SYNCOPE VASOVAGAL ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THERAPY CESSATION ( 6 FDA reports)
THREATENED LABOUR ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
TONSILLECTOMY ( 6 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 6 FDA reports)
TRACHEAL FISTULA ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRANSPLANT REJECTION ( 6 FDA reports)
ULCER HAEMORRHAGE ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 6 FDA reports)
VENTRICULAR DYSKINESIA ( 6 FDA reports)
VERBAL ABUSE ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
VITAMIN K DEFICIENCY ( 6 FDA reports)
WHIPLASH INJURY ( 6 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
SUBACUTE HEPATIC FAILURE ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
THROAT LESION ( 5 FDA reports)
THYROID ATROPHY ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TONGUE PRURITUS ( 5 FDA reports)
TONSIL CANCER ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
TRAUMATIC LUNG INJURY ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
UTERINE RUPTURE ( 5 FDA reports)
VAGINAL CYST ( 5 FDA reports)
VASCULAR CALCIFICATION ( 5 FDA reports)
VASCULAR RUPTURE ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VERBIGERATION ( 5 FDA reports)
VICTIM OF CRIME ( 5 FDA reports)
VICTIM OF HOMICIDE ( 5 FDA reports)
VISION ABNORMAL NEONATAL ( 5 FDA reports)
VITAMIN B12 DECREASED ( 5 FDA reports)
VOMITING NEONATAL ( 5 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 5 FDA reports)
VULVOVAGINAL DRYNESS ( 5 FDA reports)
YAWNING ( 5 FDA reports)
ABNORMAL CLOTTING FACTOR ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ALLERGIC COLITIS ( 5 FDA reports)
ALVEOLITIS ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 5 FDA reports)
APALLIC SYNDROME ( 5 FDA reports)
ASTHENOPIA ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 5 FDA reports)
BILE DUCT CANCER ( 5 FDA reports)
BILIARY DILATATION ( 5 FDA reports)
BLOOD CHOLESTEROL ( 5 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BODY DYSMORPHIC DISORDER ( 5 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 5 FDA reports)
BRACHIAL PLEXOPATHY ( 5 FDA reports)
BRAIN HYPOXIA ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST DISORDER ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BRONCHOSCOPY ( 5 FDA reports)
BULLOUS LUNG DISEASE ( 5 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 5 FDA reports)
CATHETER SITE PAIN ( 5 FDA reports)
CAUDA EQUINA SYNDROME ( 5 FDA reports)
CEREBRAL CALCIFICATION ( 5 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHOANAL ATRESIA ( 5 FDA reports)
CLOSTRIDIUM COLITIS ( 5 FDA reports)
COLONIC ATONY ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
COMMINUTED FRACTURE ( 5 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 5 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 5 FDA reports)
DENTAL NECROSIS ( 5 FDA reports)
DERMOID CYST ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIABETIC NEPHROPATHY ( 5 FDA reports)
DIABETIC VASCULAR DISORDER ( 5 FDA reports)
DIVERTICULAR PERFORATION ( 5 FDA reports)
DYSLALIA ( 5 FDA reports)
DYSLEXIA ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
EDENTULOUS ( 5 FDA reports)
EJACULATION DELAYED ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOCARDITIS BACTERIAL ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EXHIBITIONISM ( 5 FDA reports)
EYE INJURY ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FEBRILE INFECTION ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOOT OPERATION ( 5 FDA reports)
FOREIGN BODY REACTION ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GINGIVAL ABSCESS ( 5 FDA reports)
GRAFT COMPLICATION ( 5 FDA reports)
HAEMATOCRIT ABNORMAL ( 5 FDA reports)
HAEMOGLOBIN ABNORMAL ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HELICOBACTER TEST POSITIVE ( 5 FDA reports)
HYPERCHLORAEMIA ( 5 FDA reports)
HYPERPHOSPHATAEMIA ( 5 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 5 FDA reports)
INJECTION SITE BRUISING ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INTENTION TREMOR ( 5 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 5 FDA reports)
IRON DEFICIENCY ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LABYRINTHITIS ( 5 FDA reports)
LASER THERAPY ( 5 FDA reports)
LIMB REDUCTION DEFECT ( 5 FDA reports)
LIP OEDEMA ( 5 FDA reports)
LIPODYSTROPHY ACQUIRED ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
LYMPHOHISTIOCYTOSIS ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
MEIGE'S SYNDROME ( 5 FDA reports)
MENINGITIS VIRAL ( 5 FDA reports)
MENOMETRORRHAGIA ( 5 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MICTURITION FREQUENCY DECREASED ( 5 FDA reports)
MIGRAINE WITH AURA ( 5 FDA reports)
MYASTHENIA GRAVIS ( 5 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 5 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
NECK DEFORMITY ( 5 FDA reports)
NECK MASS ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
NEUROPATHIC ULCER ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OESOPHAGEAL SPASM ( 5 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
ONYCHOMADESIS ( 5 FDA reports)
OPISTHOTONUS ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
PARALYSIS FLACCID ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PARKINSONIAN REST TREMOR ( 5 FDA reports)
PENILE HAEMORRHAGE ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
PHANTOM PAIN ( 5 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 5 FDA reports)
PLEURAL ADHESION ( 5 FDA reports)
PLEURAL HAEMORRHAGE ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PORENCEPHALY ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POST HERPETIC NEURALGIA ( 5 FDA reports)
POST PROCEDURAL FISTULA ( 5 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
PRE-ECLAMPSIA ( 5 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 5 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 5 FDA reports)
PROCTALGIA FUGAX ( 5 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 5 FDA reports)
PROSTRATION ( 5 FDA reports)
PROTEIN URINE ( 5 FDA reports)
PULMONARY VASCULAR DISORDER ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
PURPLE GLOVE SYNDROME ( 5 FDA reports)
RADIAL NERVE PALSY ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 5 FDA reports)
SELF MUTILATION ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SINUS POLYP ( 5 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SKIN CANCER ( 5 FDA reports)
SKIN WARM ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SOCIAL PHOBIA ( 5 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 5 FDA reports)
SPINAL OPERATION ( 5 FDA reports)
SPINAL PAIN ( 5 FDA reports)
SPLINTER HAEMORRHAGES ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
ABDOMINAL INJURY ( 4 FDA reports)
ABSCESS LIMB ( 4 FDA reports)
ABULIA ( 4 FDA reports)
ACCIDENT AT HOME ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ACUTE TONSILLITIS ( 4 FDA reports)
ALCOHOLIC ( 4 FDA reports)
ALLERGY TEST POSITIVE ( 4 FDA reports)
ALVEOLAR PROTEINOSIS ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
AMPHETAMINES POSITIVE ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANAL ULCER ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ANHIDROSIS ( 4 FDA reports)
ANION GAP DECREASED ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC DILATATION ( 4 FDA reports)
AORTIC VALVE CALCIFICATION ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
APPLICATION SITE DERMATITIS ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
APPLICATION SITE VESICLES ( 4 FDA reports)
ARRESTED LABOUR ( 4 FDA reports)
ARRHYTHMIA NEONATAL ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
ASPERGER'S DISORDER ( 4 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 4 FDA reports)
AURA ( 4 FDA reports)
BALANOPOSTHITIS ( 4 FDA reports)
BARTHOLIN'S CYST ( 4 FDA reports)
BASE EXCESS DECREASED ( 4 FDA reports)
BITE ( 4 FDA reports)
BLADDER INJURY ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 4 FDA reports)
BODY FAT DISORDER ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE NEOPLASM ( 4 FDA reports)
BONE TRIMMING ( 4 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BREAST FIBROSIS ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BRONCHIAL CARCINOMA ( 4 FDA reports)
BULIMIA NERVOSA ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
BURSITIS INFECTIVE ( 4 FDA reports)
CALCULUS URINARY ( 4 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CARNITINE DECREASED ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 4 FDA reports)
CARTILAGE HYPERTROPHY ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 4 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 4 FDA reports)
CEREBELLAR ATAXIA ( 4 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBRAL THROMBOSIS ( 4 FDA reports)
CHANGE OF BOWEL HABIT ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
COPROLALIA ( 4 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYANOSIS NEONATAL ( 4 FDA reports)
CYSTITIS NONINFECTIVE ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DARK CIRCLES UNDER EYES ( 4 FDA reports)
DELIRIUM TREMENS ( 4 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 4 FDA reports)
DIABETIC GANGRENE ( 4 FDA reports)
DIAPHRAGMALGIA ( 4 FDA reports)
DISSOCIATIVE FUGUE ( 4 FDA reports)
DISTRACTIBILITY ( 4 FDA reports)
DRUG ADDICT ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
DYSKINESIA NEONATAL ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
EARLY SATIETY ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ELECTROPHORESIS ABNORMAL ( 4 FDA reports)
ENEMA ADMINISTRATION ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EOSINOPHILIC CELLULITIS ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHEMA AB IGNE ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
ESCHERICHIA BACTERAEMIA ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EXCITABILITY ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EXPOSURE TO TOXIC AGENT ( 4 FDA reports)
EXTRADURAL HAEMATOMA ( 4 FDA reports)
EYE ABSCESS ( 4 FDA reports)
EYELID OPERATION ( 4 FDA reports)
FACTITIOUS DISORDER ( 4 FDA reports)
FAT EMBOLISM ( 4 FDA reports)
FEEDING TUBE COMPLICATION ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FRACTURE DELAYED UNION ( 4 FDA reports)
GALLBLADDER ENLARGEMENT ( 4 FDA reports)
GAMMOPATHY ( 4 FDA reports)
GASTRIC HYPOMOTILITY ( 4 FDA reports)
GASTRIC PERFORATION ( 4 FDA reports)
GASTROINTESTINAL INJURY ( 4 FDA reports)
GASTROSCHISIS ( 4 FDA reports)
GLOBULINS DECREASED ( 4 FDA reports)
GLOBULINS INCREASED ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAEMORRHAGIC CYST ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HELICOBACTER GASTRITIS ( 4 FDA reports)
HELMINTHIC INFECTION ( 4 FDA reports)
HEPATIC ARTERY OCCLUSION ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 4 FDA reports)
HEREDITARY ANGIOEDEMA ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPOCHLORAEMIA ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 4 FDA reports)
IMPULSE-CONTROL DISORDER ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCREASED BRONCHIAL SECRETION ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INJECTION SITE VESICLES ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 4 FDA reports)
INTERVERTEBRAL DISC INJURY ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
KERATORHEXIS ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LEGAL PROBLEM ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LIGAMENT DISORDER ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LIPIDS ABNORMAL ( 4 FDA reports)
LIVER TENDERNESS ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LIVIDITY ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
LUNG CANCER METASTATIC ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 4 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 4 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 4 FDA reports)
MAXILLOFACIAL OPERATION ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
METHAEMOGLOBINAEMIA ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MONOCYTE COUNT ABNORMAL ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MURDER ( 4 FDA reports)
MYODESOPSIA ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NECROTISING FASCIITIS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 4 FDA reports)
NIPPLE PAIN ( 4 FDA reports)
NODAL ARRHYTHMIA ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OESOPHAGEAL RUPTURE ( 4 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC DISC DISORDER ( 4 FDA reports)
ORTHODONTIC PROCEDURE ( 4 FDA reports)
OVARIAN CANCER ( 4 FDA reports)
OVARIAN INFECTION ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PARKINSONIAN GAIT ( 4 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERIARTICULAR DISORDER ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERIPHERAL PARALYSIS ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PHOBIC AVOIDANCE ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PITUITARY TUMOUR BENIGN ( 4 FDA reports)
PLATELET AGGREGATION ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PLEURAL DECORTICATION ( 4 FDA reports)
PNEUMOBILIA ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
POLYMENORRHOEA ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
POOR PERSONAL HYGIENE ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
RECTAL CANCER STAGE IV ( 4 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 4 FDA reports)
RENAL CYST RUPTURED ( 4 FDA reports)
RETINAL VASCULAR DISORDER ( 4 FDA reports)
RETINOPATHY HYPERTENSIVE ( 4 FDA reports)
REYE'S SYNDROME ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SCAR EXCISION ( 4 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 4 FDA reports)
SCROTAL ULCER ( 4 FDA reports)
SERUM SEROTONIN DECREASED ( 4 FDA reports)
SINUS ANTROSTOMY ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN CANDIDA ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SMALL INTESTINAL STENOSIS ( 4 FDA reports)
SNAKE BITE ( 4 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 4 FDA reports)
SPINAL LAMINECTOMY ( 4 FDA reports)
SPLENIC CYST ( 4 FDA reports)
STARVATION ( 4 FDA reports)
STEM CELL TRANSPLANT ( 4 FDA reports)
STILLBIRTH ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
TENDON CALCIFICATION ( 4 FDA reports)
TERMINAL STATE ( 4 FDA reports)
TESTICULAR SWELLING ( 4 FDA reports)
TETANY ( 4 FDA reports)
THOUGHT BLOCKING ( 4 FDA reports)
TONGUE COATED ( 4 FDA reports)
TOOTH EROSION ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UMBILICAL HERNIA ( 4 FDA reports)
UNDERWEIGHT ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 4 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
URINE AMPHETAMINE POSITIVE ( 4 FDA reports)
UTERINE INFECTION ( 4 FDA reports)
VASCULAR FRAGILITY ( 4 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 4 FDA reports)
VITRITIS ( 4 FDA reports)
VOMITING IN PREGNANCY ( 4 FDA reports)
VOMITING PROJECTILE ( 4 FDA reports)
VON WILLEBRAND'S DISEASE ( 4 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 4 FDA reports)
YELLOW SKIN ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
STIFF-MAN SYNDROME ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYMPTOM MASKED ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TEETH BRITTLE ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THIRST DECREASED ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
TONGUE BLISTERING ( 3 FDA reports)
TOOTH INJURY ( 3 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINAL CANDIDIASIS ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VAGINAL ODOUR ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VICTIM OF ABUSE ( 3 FDA reports)
VITAMIN B6 DECREASED ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
VULVOVAGINAL ERYTHEMA ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WAXY FLEXIBILITY ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WEIGHT BEARING DIFFICULTY ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACROCHORDON ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENAL CORTEX ATROPHY ( 3 FDA reports)
AGNOSIA ( 3 FDA reports)
AGRAPHIA ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALOPECIA AREATA ( 3 FDA reports)
AMAUROSIS ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
ANAL ATRESIA ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
ARACHNOID CYST ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 3 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 3 FDA reports)
AV DISSOCIATION ( 3 FDA reports)
AXILLARY MASS ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BANKRUPTCY ( 3 FDA reports)
BASAL GANGLIA INFARCTION ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BEHCET'S SYNDROME ( 3 FDA reports)
BENIGN GASTRIC NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 3 FDA reports)
BEZOAR ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BIPOLAR II DISORDER ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
BLADDER TRABECULATION ( 3 FDA reports)
BLOOD BILIRUBIN ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 3 FDA reports)
BLOOD PRESSURE ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE DENSITY ABNORMAL ( 3 FDA reports)
BONE FORMATION DECREASED ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BREAST FEEDING ( 3 FDA reports)
BREAST HYPERPLASIA ( 3 FDA reports)
BREAST MICROCALCIFICATION ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHIAL SECRETION RETENTION ( 3 FDA reports)
CALCINOSIS ( 3 FDA reports)
CALCULUS URETERIC ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 3 FDA reports)
CEREBELLAR ISCHAEMIA ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CEREBRAL VASOCONSTRICTION ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COLON CANCER RECURRENT ( 3 FDA reports)
COLONIC OBSTRUCTION ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 3 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CYSTITIS INTERSTITIAL ( 3 FDA reports)
DEATH NEONATAL ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DEJA VU ( 3 FDA reports)
DELUSION OF GRANDEUR ( 3 FDA reports)
DELUSION OF REFERENCE ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 3 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 3 FDA reports)
DEVICE ADHESION ISSUE ( 3 FDA reports)
DEVICE INTERACTION ( 3 FDA reports)
DIARRHOEA NEONATAL ( 3 FDA reports)
DREAMY STATE ( 3 FDA reports)
DRUG THERAPY CHANGED ( 3 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DYSCALCULIA ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
ECLAMPSIA ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
FAECALITH ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 3 FDA reports)
FOOD AVERSION ( 3 FDA reports)
FRACTURED COCCYX ( 3 FDA reports)
FULL BLOOD COUNT INCREASED ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GASTRIC LAVAGE ( 3 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
GENITAL INFECTION BACTERIAL ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GINGIVAL ERYTHEMA ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
HAEMATOCRIT INCREASED ( 3 FDA reports)
HAEMOPERFUSION ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HEAD TITUBATION ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEART VALVE REPLACEMENT ( 3 FDA reports)
HEAT RASH ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HEPATIC HAEMATOMA ( 3 FDA reports)
HERNIA PAIN ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 3 FDA reports)
HYDROCHOLECYSTIS ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERINSULINISM ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERPLASIA ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTRICHOSIS ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOPLASTIC ANAEMIA ( 3 FDA reports)
ILEOSTOMY ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE HAEMORRHAGE ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE OEDEMA ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INJECTION SITE STINGING ( 3 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
INTERCOSTAL RETRACTION ( 3 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
INTRACRANIAL ANEURYSM ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IRIS ADHESIONS ( 3 FDA reports)
ISCHAEMIC NEPHROPATHY ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
JUGULAR VEIN DISTENSION ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LAGOPHTHALMOS ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEUKOCYTE ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
LEUKOPENIA NEONATAL ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 3 FDA reports)
LIP PAIN ( 3 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
LYMPHOCYTIC INFILTRATION ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 3 FDA reports)
MELANOSIS COLI ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
METASTASES TO RETROPERITONEUM ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MOEBIUS II SYNDROME ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NASAL CYST ( 3 FDA reports)
NECROSIS ISCHAEMIC ( 3 FDA reports)
NEONATAL ANURIA ( 3 FDA reports)
NEONATAL ASPIRATION ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
NIEMANN-PICK DISEASE ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NO ADVERSE DRUG EFFECT ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
OCULOGYRATION ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OLIGOMENORRHOEA ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORAL DISCHARGE ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORAL PAPILLOMA ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OSTEOMA ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PAIN THRESHOLD DECREASED ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PALPATORY FINDING ABNORMAL ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PANCREATICODUODENECTOMY ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARATHYROID TUMOUR ( 3 FDA reports)
PARATHYROIDECTOMY ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERIODONTAL INFECTION ( 3 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 3 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PHARYNGEAL CYST ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PLASMAPHERESIS ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
POLAND'S SYNDROME ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL CELLULITIS ( 3 FDA reports)
POST PROCEDURAL URINE LEAK ( 3 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRESCRIPTION FORM TAMPERING ( 3 FDA reports)
PROCEDURAL SITE REACTION ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 3 FDA reports)
PSEUDOLYMPHOMA ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 3 FDA reports)
PULMONARY HYPOPLASIA ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETINAL OEDEMA ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
ROSAI-DORFMAN SYNDROME ( 3 FDA reports)
SALPINGITIS ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 3 FDA reports)
SCLERAL DISCOLOURATION ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
SENILE DEMENTIA ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SIGMOIDITIS ( 3 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOFT TISSUE INFLAMMATION ( 3 FDA reports)
SPINA BIFIDA ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
SPLENIC RUPTURE ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS MANAGEMENT ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 2 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 2 FDA reports)
ACROPHOBIA ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 2 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ALCOHOL PROBLEM ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANISOCYTOSIS ( 2 FDA reports)
ANOSOGNOSIA ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTICHOLINERGIC SYNDROME ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
AORTIC VALVE PROLAPSE ( 2 FDA reports)
AORTIC VALVE REPLACEMENT ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARACHNOPHOBIA ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ARTHROSCOPY ABNORMAL ( 2 FDA reports)
ARTIFICIAL MENOPAUSE ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTHMA LATE ONSET ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURAL POLYP ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASE EXCESS ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BASILAR MIGRAINE ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN UTERINE NEOPLASM ( 2 FDA reports)
BENIGN VAGINAL NEOPLASM ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BRUCELLOSIS ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
BUTTERFLY RASH ( 2 FDA reports)
CAMPYLOBACTER INFECTION ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIORENAL SYNDROME ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CENTRAL PAIN SYNDROME ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CEREBROSPINAL FLUID DRAINAGE ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLESTEROL GRANULOMA ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CITROBACTER TEST POSITIVE ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
COAGULATION TEST ABNORMAL ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COLON CANCER STAGE II ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL BLADDER ANOMALY ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL NOSE MALFORMATION ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COPPER DEFICIENCY ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CROSSMATCH INCOMPATIBLE ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DENTAL FLUORIDE THERAPY ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DEXTROCARDIA ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC MICROANGIOPATHY ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DRUG LEVEL FLUCTUATING ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER REPAIR ( 2 FDA reports)
DYSLOGIA ( 2 FDA reports)
EAR ABRASION ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIAL DISORDER ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENDOTOXIC SHOCK ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
EPILEPTIC AURA ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EXTRUSION OF DEVICE ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
EYE NAEVUS ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FLOPPY IRIS SYNDROME ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FORCEPS DELIVERY ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC OPERATION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX PROPHYLAXIS ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GIARDIASIS ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL PRURITUS ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOBAL AMNESIA ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEAD BANGING ( 2 FDA reports)
HEART TRANSPLANT ( 2 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERSPLENISM ACQUIRED ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTRICHOSIS ( 2 FDA reports)
IDEAS OF REFERENCE ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE FIBROSIS ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 2 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
JAW CYST ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT INSTABILITY ( 2 FDA reports)
JOINT WARMTH ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
JUVENILE ARTHRITIS ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KNEE DEFORMITY ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGAMENT INJURY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOSUCTION ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LORDOSIS ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALIGNANT MELANOMA STAGE II ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MATERNAL ALCOHOL USE ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENTALLY LATE DEVELOPER ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METABOLIC MYOPATHY ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO CHEST WALL ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MILD MENTAL RETARDATION ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NECROTISING RETINITIS ( 2 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 2 FDA reports)
NEPHROCALCINOSIS ( 2 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 2 FDA reports)
NERVE ROOT COMPRESSION ( 2 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ONYCHOPHAGIA ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
ORGASMIC SENSATION DECREASED ( 2 FDA reports)
OROMANDIBULAR DYSTONIA ( 2 FDA reports)
OSTEOGENESIS IMPERFECTA ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
OVARIAN MASS ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PELVIC CONGESTION ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 2 FDA reports)
PHAEHYPHOMYCOSIS ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA LIPOID ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYMEDICATION ( 2 FDA reports)
POOR DENTAL CONDITION ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE HERNIA ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 2 FDA reports)
PRECANCEROUS CELLS PRESENT ( 2 FDA reports)
PRECOCIOUS PUBERTY ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRODUCT COLOUR ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT COUNTERFEIT ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDOALDOSTERONISM ( 2 FDA reports)
PSEUDOMENINGOCELE ( 2 FDA reports)
PSEUDOPARALYSIS ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PSYCHOMOTOR SEIZURES ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY DYSMATURITY SYNDROME ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PYRUVATE KINASE INCREASED ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RADIOTHERAPY TO BRAIN ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RED BLOOD CELLS SEMEN ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
REITER'S SYNDROME ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL FAILURE NEONATAL ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RETINAL DEGENERATION ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
SALIVA ALTERED ( 2 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SENSATION OF BLOOD FLOW ( 2 FDA reports)
SENSATION OF PRESSURE IN EAR ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SEPSIS NEONATAL ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SEVERE MENTAL RETARDATION ( 2 FDA reports)
SEXUAL ABUSE ( 2 FDA reports)
SEXUAL OFFENCE ( 2 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SINUS PERFORATION ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP STUDY ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SOMATOFORM DISORDER PREGNANCY ( 2 FDA reports)
SPASTIC PARAPLEGIA ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPERMATOZOA ABNORMAL ( 2 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 2 FDA reports)
SPINAL CORD DRAINAGE ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPINDLE CELL SARCOMA ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPLENITIS ( 2 FDA reports)
STAB WOUND ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 2 FDA reports)
THYMOL TURBIDITY TEST INCREASED ( 2 FDA reports)
TINEA CRURIS ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TONSILLITIS BACTERIAL ( 2 FDA reports)
TOOTH REPAIR ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TOTAL HYSTERECTOMY ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRANSURETHRAL RESECTION SYNDROME ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TRYPTASE ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
URINOMA ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VENTRICULAR FLUTTER ( 2 FDA reports)
VENTRICULAR HYPOPLASIA ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VIRAL PHARYNGITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 2 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 2 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
VOCAL CORD DISORDER ( 2 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 2 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
X-RAY LIMB ABNORMAL ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STEREOTYPIC MOVEMENT DISORDER ( 1 FDA reports)
STIFF PERSON SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SURFACTANT PROTEIN INCREASED ( 1 FDA reports)
SURGICAL VASCULAR SHUNT ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TARSAL TUNNEL DECOMPRESSION ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDINOUS CONTRACTURE ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON REPAIR ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR OPERATION ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 1 FDA reports)
TETANUS ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC HYPOTHERMIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS PELVIC VEIN ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID MASS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROIDITIS ACUTE ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TOLOSA-HUNT SYNDROME ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOTAL BILE ACIDS INCREASED ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 1 FDA reports)
TOURETTE'S DISORDER ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT HYPOGAMMAGLOBULINAEMIA OF INFANCY ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 1 FDA reports)
TRANSVERSE PRESENTATION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYMPANOPLASTY ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND FOETAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URETHRAL STRICTURE ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY ANASTOMOTIC LEAK ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE DELTA AMINOLEVULINATE ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE SODIUM ( 1 FDA reports)
URINE SODIUM ABNORMAL ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULAR TEST ABNORMAL ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOMOUS BITE ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VICTIM OF SEXUAL ABUSE ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B1 DECREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT DECREASE NEONATAL ( 1 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WITHDRAWAL BLEED ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
XANTHOCHROMIA ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
ABDOMEN CRUSHING ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADENOTONSILLECTOMY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGIC BRONCHITIS ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMOEBIC DYSENTERY ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANOTIA ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANXIOLYTIC THERAPY ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PHOTOSENSITIVITY REACTION ( 1 FDA reports)
APPLICATION SITE PUSTULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AVOIDANT PERSONALITY DISORDER ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND SENSATION ( 1 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BINGE DRINKING ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALCOHOL ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD KETONE BODY DECREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD LEAD ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BORDERLINE MENTAL IMPAIRMENT ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN LOBECTOMY ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CALCULUS URETHRAL ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMYOPATHY NEONATAL ( 1 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATAXIA ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMANGIOMA ( 1 FDA reports)
CEREBRAL REVASCULARISATION SYNANGIOSIS ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHEMICAL ABUSER ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHLOASMA ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CHOROID PLEXUS PAPILLOMA ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHYLOMICRON INCREASED ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLON OPERATION ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMA BLISTER ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL DEFORMITY OF CLAVICLE ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NAIL DISORDER ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COPROPORPHYRINOGEN INCREASED ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL LEUKOMA ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CRYSTAL URINE ABSENT ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYSTIC FIBROSIS LUNG ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEATH OF CHILD ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF FRIEND ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DECREASED VENTRICULAR AFTERLOAD ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE BATTERY ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALOCELE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
ERYTHROMELALGIA ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERTIONAL HEADACHE ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EXTRAVASATION OF URINE ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL PERIODIC PARALYSIS ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF EATING ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FIBROUS HISTIOCYTOMA ( 1 FDA reports)
FINGER HYPOPLASIA ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLYCOSURIA DURING PREGNANCY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHAGIC URTICARIA ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERNIA CONGENITAL ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HIV INFECTION CDC CATEGORY C3 ( 1 FDA reports)
HOLMES TREMOR ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HUNTINGTON'S DISEASE ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSTHENURIA ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYSTERICAL PSYCHOSIS ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOLOGY TEST ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPLANT OBSTRUCTION ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 1 FDA reports)
INTERNAL FIXATION OF SPINE ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JEJUNECTOMY ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT RESURFACING SURGERY ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
KIDNEY PERFORATION ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
KYPHOSIS CONGENITAL ( 1 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGECTOMY ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 1 FDA reports)
LEVATOR SYNDROME ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR CYST ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MACULE ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTOIDECTOMY ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECONIUM INCREASED ( 1 FDA reports)
MEDIAN NERVE INJURY ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDULLARY THYROID CANCER ( 1 FDA reports)
MELAENA NEONATAL ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROENCEPHALY ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MIDDLE EAR PROSTHESIS INSERTION ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUCKLE-WELLS SYNDROME ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MULTIPLE CARDIAC DEFECTS ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYELOCYTE PRESENT ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL GROWTH CESSATION ( 1 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 1 FDA reports)
NEONATAL DIABETES MELLITUS ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEOPLASM PROSTATE ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE GRAFT ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL CYST ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
OVARIAN HAEMATOMA ( 1 FDA reports)
OVARIAN NECROSIS ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANOID PERSONALITY DISORDER ( 1 FDA reports)
PARAPROTEINAEMIA ( 1 FDA reports)
PARASITE DNA TEST POSITIVE ( 1 FDA reports)
PARKINSONIAN CRISIS ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PAROXYSMAL PERCEPTUAL ALTERATION ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERINATAL BRAIN DAMAGE ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGEAL OPERATION ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY ENLARGEMENT ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PODAGRA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST LAMINECTOMY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POSTPARTUM DEPRESSION ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTHESIS USER ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUTAMEN HAEMORRHAGE ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RECTAL TUBE INSERTION ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DYSTROPHY ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RETROPLACENTAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SALT INTOXICATION ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SECONDARY SEQUESTRUM ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SILICON GRANULOMA ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY THORACIC ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)