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

HYPOTENSION ( 27 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
PNEUMONIA ( 11 FDA reports)
ANAEMIA ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
SICK SINUS SYNDROME ( 9 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SHOCK ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMPLANT SITE NECROSIS ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS ALLERGIC ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE INJURY ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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