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

DYSPNOEA ( 6 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
DEPRESSION ( 3 FDA reports)
FALL ( 3 FDA reports)
HERNIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DRESSLER'S SYNDROME ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GOUT ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOPHOBIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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