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

HYPOTENSION ( 45 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 35 FDA reports)
CARDIAC ARREST ( 33 FDA reports)
PULMONARY EMBOLISM ( 28 FDA reports)
DRUG INEFFECTIVE ( 26 FDA reports)
DYSPNOEA ( 23 FDA reports)
ASTHENIA ( 21 FDA reports)
BLINDNESS ( 19 FDA reports)
RESPIRATORY FAILURE ( 19 FDA reports)
BLOOD PRESSURE DECREASED ( 18 FDA reports)
OVERDOSE ( 18 FDA reports)
HAEMODYNAMIC INSTABILITY ( 17 FDA reports)
MULTI-ORGAN FAILURE ( 17 FDA reports)
TACHYCARDIA ( 17 FDA reports)
DRUG TOXICITY ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
DEATH ( 15 FDA reports)
MYOCARDIAL INFARCTION ( 15 FDA reports)
CARDIAC FAILURE ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
VISUAL ACUITY REDUCED ( 12 FDA reports)
HYPOGLYCAEMIA ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
SHOCK ( 11 FDA reports)
BRADYCARDIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
RETINAL INJURY ( 9 FDA reports)
RETINOGRAM ABNORMAL ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
CORNEAL ABRASION ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
SINUS TACHYCARDIA ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
ENTEROCOCCAL INFECTION ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
IRIDOCYCLITIS ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
POST PROCEDURAL BILE LEAK ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
COMA ( 5 FDA reports)
HYSTERECTOMY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
TREMOR ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARTERIAL LIGATION ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
CARDIAC MASSAGE ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CAROTID PULSE DECREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PULSE PRESSURE DECREASED ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
ISCHAEMIC HEPATITIS ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
ULCER ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOKING ( 2 FDA reports)
COAGULATION FACTOR INCREASED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 2 FDA reports)
KOUNIS SYNDROME ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTERIOR CHAMBER DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE NECROSIS ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMPLANT SITE ULCER ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INSTILLATION SITE REACTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGITIS FUNGAL ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTEIN ALBUMIN RATIO INCREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROSEOLA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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