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

PNEUMONIA ( 6 FDA reports)
LIVER DISORDER ( 5 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FALL ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use