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

MYOCARDIAL INFARCTION ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
RETINAL ARTERY OCCLUSION ( 6 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
DEATH ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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