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

HAEMATOMA ( 4 FDA reports)
SYNCOPE ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
FALL ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEATH ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)

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