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

HYPOTENSION ( 16 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
ENTEROCOCCAL INFECTION ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
FALL ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLON CANCER STAGE III ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
POSTOPERATIVE ILEUS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INTERVERTEBRAL DISC INJURY ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SCAR ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STARING ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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