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

VOMITING ( 11 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
DIARRHOEA ( 7 FDA reports)
MALIGNANT MELANOMA ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
INSOMNIA ( 5 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SUTURE RELATED COMPLICATION ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
RASH ( 2 FDA reports)
SLEEP WALKING ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IUD MIGRATION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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