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

HYPERTENSION ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INTRACRANIAL ANEURYSM ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
ANGER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARASITIC GASTROENTERITIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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