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HYPERTENSION ( 4 FDA reports)
SYNCOPE ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
CRYING ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SWELLING ( 1 FDA reports)
AGITATION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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