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

ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
FALL ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)

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