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

HYPOTENSION ( 68 FDA reports)
DRUG INTERACTION ( 43 FDA reports)
ANAPHYLACTIC REACTION ( 40 FDA reports)
BRADYCARDIA ( 38 FDA reports)
CARDIAC ARREST ( 29 FDA reports)
OXYGEN SATURATION DECREASED ( 28 FDA reports)
SEPSIS ( 27 FDA reports)
HYPERTENSION ( 25 FDA reports)
BRONCHOSPASM ( 23 FDA reports)
RESPIRATORY FAILURE ( 21 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
PULMONARY OEDEMA ( 19 FDA reports)
RENAL FAILURE ACUTE ( 19 FDA reports)
VENTRICULAR FIBRILLATION ( 19 FDA reports)
ANAESTHETIC COMPLICATION ( 18 FDA reports)
CYANOSIS ( 18 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
OVERDOSE ( 18 FDA reports)
POST PROCEDURAL COMPLICATION ( 18 FDA reports)
RENAL FAILURE ( 18 FDA reports)
TACHYCARDIA ( 18 FDA reports)
AGITATION ( 17 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
WRONG DRUG ADMINISTERED ( 17 FDA reports)
HYPOXIA ( 16 FDA reports)
ANAPHYLACTIC SHOCK ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 15 FDA reports)
HYPERGLYCAEMIA ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
SEROTONIN SYNDROME ( 15 FDA reports)
VOMITING ( 15 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
DYSKINESIA ( 14 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
RESPIRATORY ACIDOSIS ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
DISORIENTATION ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
RHABDOMYOLYSIS ( 11 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
BRADYCARDIA NEONATAL ( 10 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 10 FDA reports)
HYPERCAPNIA ( 10 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
PARALYSIS FLACCID ( 10 FDA reports)
PROPOFOL INFUSION SYNDROME ( 10 FDA reports)
PULSE ABSENT ( 10 FDA reports)
RESPIRATORY ARREST ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CARDIO-RESPIRATORY ARREST ( 9 FDA reports)
COMA ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
APNOEA ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
CHILLS ( 8 FDA reports)
CYANOSIS NEONATAL ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
NEONATAL DISORDER ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
RASH ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPERPYREXIA ( 7 FDA reports)
HYPERTONIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PAIN ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
RESUSCITATION ( 7 FDA reports)
SHOCK ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
ANGIOEDEMA ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CONVERSION DISORDER ( 6 FDA reports)
COUGH ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
DYSTONIA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
UNRESPONSIVE TO STIMULI ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CLONUS ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERTHERMIA MALIGNANT ( 5 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 5 FDA reports)
INFANTILE APNOEIC ATTACK ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
INJURY ( 5 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NEONATAL RESPIRATORY ARREST ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SEDATION ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANAPHYLACTOID SHOCK ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEAR ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CYTOKINE RELEASE SYNDROME ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEVICE INEFFECTIVE ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EFFECT PROLONGED ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HYPOTONIA NEONATAL ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
INTUBATION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MASTOCYTOSIS ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 3 FDA reports)
VASODILATATION ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 2 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CAPILLARY DISORDER ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DUODENAL POLYP ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
FALL ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PITYRIASIS ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD ISCHAEMIA ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOLISTHESIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINOMA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAL DILATATION ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW NECROSIS ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMA NEONATAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONUS MEDULLARIS SYNDROME ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORONA VIRUS INFECTION ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSIVE DELUSION ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEOPLASM SWELLING ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PENILE VASCULAR DISORDER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL NAUSEA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENT ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECURRENCE OF NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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