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

BLOOD PRESSURE INCREASED ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PAIN ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
ASTHENIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
ABASIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use