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

FLUSHING ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
AORTIC STENOSIS ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
DEATH ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FEAR ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INJURY ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
STRESS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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