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

VOMITING ( 3 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 3 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
INJECTION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHILLS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
CHOLESTASIS OF PREGNANCY ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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