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CYTOLYTIC HEPATITIS ( 19 FDA reports)
CHOLESTASIS ( 13 FDA reports)
AGITATION ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPTIC NERVE CUPPING ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APOPTOSIS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHLAMYDIA TEST POSITIVE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CATARACT ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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