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

THROMBOCYTOPENIA ( 7 FDA reports)
RASH ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
SWELLING ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHILLS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST-TRAUMATIC SYNDROME ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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