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

ABDOMINAL PAIN LOWER ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
VOMITING ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MENINGITIS MENINGOCOCCAL ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
COUGH ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FATIGUE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)

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