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

ANAEMIA ( 36 FDA reports)
HAEMOGLOBIN DECREASED ( 30 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
RASH ( 20 FDA reports)
NAUSEA ( 13 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
RENAL DISORDER ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
MALAISE ( 7 FDA reports)
SKIN DISORDER ( 6 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
AMYLASE INCREASED ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
MUSCLE CRAMP ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHILLS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CONGENITAL OESOPHAGEAL ANOMALY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)

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