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

DYSPNOEA ( 48 FDA reports)
CHEST PAIN ( 29 FDA reports)
BLOOD PRESSURE DECREASED ( 22 FDA reports)
RESPIRATORY ARREST ( 22 FDA reports)
TREMOR ( 20 FDA reports)
NAUSEA ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 17 FDA reports)
CARDIAC ARREST ( 17 FDA reports)
BODY TEMPERATURE INCREASED ( 16 FDA reports)
BRONCHOSPASM ( 15 FDA reports)
INFUSION RELATED REACTION ( 15 FDA reports)
CHILLS ( 14 FDA reports)
DIZZINESS ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
VOMITING ( 13 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
ARTERIOSPASM CORONARY ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
HYPERTENSION ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
PAIN IN JAW ( 7 FDA reports)
POST PROCEDURAL COMPLICATION ( 7 FDA reports)
ANXIETY ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
CORONARY ARTERY STENOSIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
LACRIMATION INCREASED ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
PANIC REACTION ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
AURA ( 4 FDA reports)
BACTERIAL CULTURE POSITIVE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RETCHING ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SLEEP STUDY ABNORMAL ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VOCAL CORD DISORDER ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VENTRICULAR ASYSTOLE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST WALL ABSCESS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)

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