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

PYREXIA ( 8 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 6 FDA reports)
URETHRAL INJURY ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
VOMITING ( 4 FDA reports)
COUGH ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
ORAL HERPES ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SCAR ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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