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

PULMONARY EMBOLISM ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
MYALGIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
ABORTION ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)

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