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

FATIGUE ( 7 FDA reports)
DEATH ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FALL ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INJURY ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
SALIVARY GLAND NEOPLASM ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CATARACT NUCLEAR ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
RALES ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CILIARY HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)

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