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

PRURITUS ( 9 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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