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

DEATH ( 48 FDA reports)
HEADACHE ( 14 FDA reports)
INFUSION RELATED REACTION ( 13 FDA reports)
FATIGUE ( 12 FDA reports)
VOMITING ( 12 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DYSPNOEA ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHILLS ( 4 FDA reports)
EXTERNAL EAR PAIN ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COUGH ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
INFUSION SITE PRURITUS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
VASCULAR DISSECTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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