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

PAIN ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ABASIA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STRESS ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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