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

VOMITING ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
COUGH ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
INJECTION SITE MASS ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
RASH ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
DYSPEPSIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
DEATH ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)

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