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

PNEUMONIA ( 32 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 17 FDA reports)
PYREXIA ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
RASH ( 13 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
HEPATITIS TOXIC ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
CULTURE STOOL POSITIVE ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 9 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
ACUTE RESPIRATORY FAILURE ( 8 FDA reports)
CHOLESTASIS ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
QUADRIPARESIS ( 7 FDA reports)
THYROTOXIC CRISIS ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
AUTOIMMUNE THYROIDITIS ( 6 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 6 FDA reports)
BLISTER ( 6 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
KLEBSIELLA INFECTION ( 6 FDA reports)
KLEBSIELLA TEST POSITIVE ( 6 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
POLYNEUROPATHY ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
COLECTOMY ( 4 FDA reports)
DEVICE RELATED SEPSIS ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EXTREMITY NECROSIS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
POST PROCEDURAL URINE LEAK ( 4 FDA reports)
PYELONEPHRITIS ACUTE ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
STRESS CARDIOMYOPATHY ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
ATRIAL PRESSURE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
EYELID PTOSIS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LINEAR IGA DISEASE ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MILLER FISHER SYNDROME ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMONIA LEGIONELLA ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INFANTILE APNOEIC ATTACK ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LARYNGITIS BACTERIAL ( 2 FDA reports)
LARYNGITIS FUNGAL ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AEROMONA INFECTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BACTERIAL TRANSLOCATION ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GENITAL INFECTION FUNGAL ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJURY ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO ABDOMINAL WALL ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA RESECTABLE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN INDUCED BY VITAMIN K ABSENCE OR ANTAGONIST II INCREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL IMPAIRMENT NEONATAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERAL NECROSIS ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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