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

ANAEMIA ( 9 FDA reports)
ANAL HAEMORRHAGE ( 9 FDA reports)
ARTHRALGIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
CROHN'S DISEASE ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
FLANK PAIN ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
GROIN PAIN ( 9 FDA reports)
ILEITIS ( 9 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
MULTI-ORGAN DISORDER ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
BONE DISORDER ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
ACNE ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANORECTAL DISCOMFORT ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
RASH ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
SCAR ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHONDROMALACIA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSYCHOLOGICAL FACTOR AFFECTING MEDICAL CONDITION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)

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