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

HAEMOGLOBIN DECREASED ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHOLECYSTITIS CHRONIC ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FISTULA ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SWELLING ( 3 FDA reports)
ADNEXA UTERI MASS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 2 FDA reports)
RASH ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
MANIA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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