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

VOMITING ( 4 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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