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

PYREXIA ( 17 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
CYTOLYTIC HEPATITIS ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
CHOLESTASIS ( 8 FDA reports)
FALL ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
SHOCK ( 5 FDA reports)
STATUS EPILEPTICUS ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
BENCE JONES PROTEINURIA ( 3 FDA reports)
BLADDER CATHETERISATION ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CSF PH DECREASED ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PSYCHOMOTOR RETARDATION ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BARBITURATES POSITIVE ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBELLAR HYPOPLASIA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COMA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATIC PAIN ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERGLOBULINAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
TERATOSPERMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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