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

ANGIONEUROTIC OEDEMA ( 5 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
NAUSEA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
HEADACHE ( 1 FDA reports)

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