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

CONVULSION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPENDYMOMA MALIGNANT ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
STARING ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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