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

PSORIASIS ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
LATENT TUBERCULOSIS ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
AGITATION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
CONTUSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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