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INFLAMMATORY BOWEL DISEASE ( 13 FDA reports)
DEPRESSION ( 10 FDA reports)
STRESS ( 8 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
COLITIS ULCERATIVE ( 7 FDA reports)
CROHN'S DISEASE ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
RASH ( 7 FDA reports)
XEROSIS ( 7 FDA reports)
APHTHOUS STOMATITIS ( 6 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
INGROWN HAIR ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
LIP DRY ( 5 FDA reports)
RECTAL POLYP ( 5 FDA reports)
SACROILIITIS ( 5 FDA reports)
UTERINE PERFORATION ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PELVIC PAIN ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ACNE ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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