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

ANAEMIA ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
CONSTIPATION ( 8 FDA reports)
DIZZINESS ( 7 FDA reports)
AMNESIA ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSMENORRHOEA ( 6 FDA reports)
FALLOPIAN TUBE OPERATION ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OVARIAN MASS ( 6 FDA reports)
PAIN ( 6 FDA reports)
POSTPARTUM HAEMORRHAGE ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
UMBILICAL CORD ABNORMALITY ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
FIBROUS HISTIOCYTOMA ( 5 FDA reports)
HAEMANGIOMA OF SKIN ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OTITIS MEDIA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
ULCER ( 5 FDA reports)
URINARY TRACT DISORDER ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CAROTID BRUIT ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ARTHROPOD BITE ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ACNE ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLESTEROSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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