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

DYSPNOEA ( 14 FDA reports)
DISORIENTATION ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
FALL ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
COUGH ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PROCTOCOLITIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SKIN TIGHTNESS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHROANGIOSCLEROSIS ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPEUTIC AGENT URINE POSITIVE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use