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

PYREXIA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DEPRESSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
NOREPINEPHRINE DECREASED ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
THIRST ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
ABASIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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