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

GASTROINTESTINAL DISORDER ( 6 FDA reports)
PORTAL HYPERTENSION ( 6 FDA reports)
MALAISE ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
RASH ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOMA AIDS RELATED ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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