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

ANXIETY ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HYPERCOAGULATION ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METAPLASIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABORTION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AURA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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