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

PAIN ( 12 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
INJECTION SITE PAIN ( 9 FDA reports)
DYSPNOEA ( 8 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
DISCOMFORT ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INJECTION SITE PARAESTHESIA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
COUGH ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
BONE LESION ( 4 FDA reports)
BITE ( 3 FDA reports)
DEATH ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
QUALITY OF LIFE DECREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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