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

HAEMOGLOBIN DECREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
HAEMATOMA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
AGITATION ( 1 FDA reports)

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