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GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
ARTHRALGIA ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
NAUSEA ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
PSORIASIS ( 9 FDA reports)
BLISTER ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
TRANSAMINASES INCREASED ( 8 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VOMITING ( 7 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPERVENTILATION ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
ECZEMA NUMMULAR ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BREAST DISCHARGE ( 4 FDA reports)
BURNOUT SYNDROME ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
ARTHRITIS ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
INDURATION ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
RASH ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TRISOMY 21 ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RALES ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHROSCOPY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)

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