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

PNEUMONIA ( 82 FDA reports)
PYREXIA ( 77 FDA reports)
INFUSION RELATED REACTION ( 69 FDA reports)
RESPIRATORY FAILURE ( 66 FDA reports)
URTICARIA ( 55 FDA reports)
OXYGEN SATURATION DECREASED ( 54 FDA reports)
VOMITING ( 48 FDA reports)
DYSPNOEA ( 43 FDA reports)
DISEASE PROGRESSION ( 40 FDA reports)
RESPIRATORY DISTRESS ( 39 FDA reports)
TACHYCARDIA ( 37 FDA reports)
CARDIAC FAILURE ( 34 FDA reports)
CARDIO-RESPIRATORY ARREST ( 33 FDA reports)
DIARRHOEA ( 33 FDA reports)
COUGH ( 32 FDA reports)
CYANOSIS ( 30 FDA reports)
HEADACHE ( 30 FDA reports)
HYDROCEPHALUS ( 30 FDA reports)
PALLOR ( 30 FDA reports)
CHILLS ( 29 FDA reports)
INFLUENZA ( 29 FDA reports)
CONVULSION ( 28 FDA reports)
HYPERTENSION ( 27 FDA reports)
CARDIAC ARREST ( 26 FDA reports)
DEATH ( 26 FDA reports)
TACHYPNOEA ( 24 FDA reports)
HYPOTENSION ( 22 FDA reports)
RESPIRATORY ARREST ( 22 FDA reports)
RASH ( 21 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 21 FDA reports)
URINARY GLYCOSAMINOGLYCANS INCREASED ( 21 FDA reports)
IRRITABILITY ( 20 FDA reports)
RESPIRATORY DISORDER ( 20 FDA reports)
CONDITION AGGRAVATED ( 19 FDA reports)
MUCOPOLYSACCHARIDOSIS I ( 19 FDA reports)
STEM CELL TRANSPLANT ( 19 FDA reports)
GRAFT VERSUS HOST DISEASE ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
BRONCHOPNEUMONIA ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
DRUG INEFFECTIVE ( 16 FDA reports)
HEART RATE INCREASED ( 16 FDA reports)
HYPERSENSITIVITY ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
BONE MARROW TRANSPLANT ( 15 FDA reports)
ASTHMA ( 14 FDA reports)
BODY TEMPERATURE INCREASED ( 14 FDA reports)
BRONCHOSPASM ( 14 FDA reports)
CARDIAC DISORDER ( 14 FDA reports)
FATIGUE ( 14 FDA reports)
WHEEZING ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
BLINDNESS ( 13 FDA reports)
FALL ( 13 FDA reports)
POOR VENOUS ACCESS ( 13 FDA reports)
VIRAL INFECTION ( 13 FDA reports)
CATHETER RELATED COMPLICATION ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
MALAISE ( 12 FDA reports)
SLEEP APNOEA SYNDROME ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 11 FDA reports)
POST PROCEDURAL COMPLICATION ( 11 FDA reports)
PROCEDURAL COMPLICATION ( 11 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
ABASIA ( 10 FDA reports)
ANAEMIA ( 10 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BRADYCARDIA ( 10 FDA reports)
CARDIAC VALVE DISEASE ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
INFECTION ( 10 FDA reports)
PNEUMONIA ASPIRATION ( 10 FDA reports)
PNEUMONIA VIRAL ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
ASPIRATION ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
MOANING ( 9 FDA reports)
TREMOR ( 9 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
ASCITES ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
CARPAL TUNNEL SYNDROME ( 8 FDA reports)
CORNEAL TRANSPLANT ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HYPERNATRAEMIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
PAPULE ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
AGITATION ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 7 FDA reports)
CENTRAL LINE INFECTION ( 7 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
DEAFNESS ( 7 FDA reports)
EAR INFECTION ( 7 FDA reports)
LIP SWELLING ( 7 FDA reports)
LIVEDO RETICULARIS ( 7 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PULMONARY HAEMORRHAGE ( 7 FDA reports)
RASH MORBILLIFORM ( 7 FDA reports)
RESPIRATORY RATE INCREASED ( 7 FDA reports)
RESPIRATORY TRACT INFECTION ( 7 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 6 FDA reports)
CATHETER SITE INFECTION ( 6 FDA reports)
CATHETER SITE OEDEMA ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
PAIN ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
ANOXIC ENCEPHALOPATHY ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 5 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CATHETER SEPSIS ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
DEFAECATION URGENCY ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MACROGLOSSIA ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
SELF-MEDICATION ( 5 FDA reports)
SNORING ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL CORD INFARCTION ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
ADENOIDAL HYPERTROPHY ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
CAPILLARY LEAK SYNDROME ( 4 FDA reports)
CARDIAC PSEUDOANEURYSM ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COMA ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
KYPHOSCOLIOSIS ( 4 FDA reports)
MUCOPOLYSACCHARIDOSIS IH ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SHUNT OCCLUSION ( 4 FDA reports)
SIALOADENITIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CERVICAL CORD COMPRESSION ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 3 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DESMOID TUMOUR ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ADENOIDAL DISORDER ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRAIN STEM GLIOMA ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS INFECTION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROSTRATION ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULOPERITONEAL SHUNT MALFUNCTION ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HERNIA GANGRENOUS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHORIORETINAL ATROPHY ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL DEFECT ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTROPHIC CALCIFICATION ( 1 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLOPPY INFANT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE OEDEMA ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS IH/S ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DRUG ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE NEUROSTIMULATION ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA MORAXELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POSTOPERATIVE STITCH SINUS ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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