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

CARDIAC DISORDER ( 4 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
DENTAL OPERATION ( 2 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)

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