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

DYSPNOEA ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
RENAL FAILURE ( 26 FDA reports)
RENAL FAILURE ACUTE ( 25 FDA reports)
HYPOTENSION ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 19 FDA reports)
DEHYDRATION ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
CHILLS ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 16 FDA reports)
CONDITION AGGRAVATED ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
DIZZINESS ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
INFECTION ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
HEADACHE ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
VOMITING ( 12 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PAIN ( 10 FDA reports)
RASH ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
AGITATION ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
COUGH ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RALES ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANURIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GOUT ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TONGUE OEDEMA ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIODONTAL DISEASE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VENOUS OCCLUSION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WALKING AID USER ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ALVEOLOPLASTY ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CHARLES BONNET SYNDROME ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INFECTION MASKED ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MACROGLOSSIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
ORBITAL OEDEMA ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPLENIC HAEMORRHAGE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUBMANDIBULAR MASS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS MANAGEMENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LENS IMPLANT ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 1 FDA reports)
SECONDARY HYPOGONADISM ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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