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

ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
RASH ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SNORING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC ENZYMES DECREASED ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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