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

DRUG INTERACTION ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
TOE OPERATION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)

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