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

PAIN ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
HEADACHE ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
BALANCE DISORDER ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
BLINDNESS ( 10 FDA reports)
CHILLS ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
UNEVALUABLE EVENT ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
NERVOUSNESS ( 8 FDA reports)
SEXUAL DYSFUNCTION ( 8 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
ERECTILE DYSFUNCTION ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MUSCLE ATROPHY ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INJECTION SITE DISCOMFORT ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PARESIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PROCEDURAL SITE REACTION ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ENDOCRINE NEOPLASM MALIGNANT ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
PROLACTIN-PRODUCING PITUITARY TUMOUR ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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