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

PYREXIA ( 50 FDA reports)
PNEUMONIA ( 40 FDA reports)
HYPOTENSION ( 36 FDA reports)
RENAL FAILURE ( 36 FDA reports)
PAIN ( 34 FDA reports)
DYSPNOEA ( 32 FDA reports)
ANXIETY ( 31 FDA reports)
ANAEMIA ( 30 FDA reports)
INJURY ( 30 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
INFECTION ( 25 FDA reports)
RASH ( 25 FDA reports)
DIARRHOEA ( 24 FDA reports)
HYPOXIA ( 24 FDA reports)
MULTI-ORGAN FAILURE ( 23 FDA reports)
HEADACHE ( 22 FDA reports)
SEPSIS ( 21 FDA reports)
PLEURAL EFFUSION ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 19 FDA reports)
DISEASE PROGRESSION ( 18 FDA reports)
HERPES ZOSTER ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
BONE DISORDER ( 17 FDA reports)
IMPAIRED HEALING ( 17 FDA reports)
MASTICATION DISORDER ( 17 FDA reports)
ORAL DISCOMFORT ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 17 FDA reports)
GASTROINTESTINAL DISORDER ( 16 FDA reports)
GINGIVITIS ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
SEPTIC SHOCK ( 16 FDA reports)
STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
STEM CELL TRANSPLANT ( 16 FDA reports)
STOMATITIS ( 16 FDA reports)
TOOTH EXTRACTION ( 16 FDA reports)
ABSCESS ( 15 FDA reports)
ARTHRALGIA ( 15 FDA reports)
ATRIAL FIBRILLATION ( 15 FDA reports)
BONE CYST ( 15 FDA reports)
BONE LESION ( 15 FDA reports)
BONE PAIN ( 15 FDA reports)
COUGH ( 15 FDA reports)
DEATH ( 15 FDA reports)
FEBRILE NEUTROPENIA ( 15 FDA reports)
GINGIVAL EROSION ( 15 FDA reports)
GINGIVAL PAIN ( 15 FDA reports)
GINGIVAL SWELLING ( 15 FDA reports)
HYPERKALAEMIA ( 15 FDA reports)
INFLUENZA LIKE ILLNESS ( 15 FDA reports)
MOUTH HAEMORRHAGE ( 15 FDA reports)
MYALGIA ( 15 FDA reports)
ORAL DISORDER ( 15 FDA reports)
PLASMACYTOMA ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
RETINAL INFARCTION ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
TONGUE INJURY ( 15 FDA reports)
TOOTH FRACTURE ( 15 FDA reports)
VAGINAL HAEMORRHAGE ( 15 FDA reports)
WOUND COMPLICATION ( 15 FDA reports)
WOUND SECRETION ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
ALOPECIA ( 14 FDA reports)
ANHEDONIA ( 14 FDA reports)
BLOOD CALCIUM DECREASED ( 14 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
HYPERTENSION ( 14 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 14 FDA reports)
ORAL SURGERY ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
LUNG DISORDER ( 13 FDA reports)
NEOPLASM MALIGNANT ( 13 FDA reports)
TOOTH DISORDER ( 13 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 13 FDA reports)
BRONCHIECTASIS ( 12 FDA reports)
DIALYSIS ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 12 FDA reports)
TRANSFUSION ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
VISUAL IMPAIRMENT ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
ENTEROCOCCAL INFECTION ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 11 FDA reports)
MENTAL STATUS CHANGES ( 11 FDA reports)
SPLENOMEGALY ( 11 FDA reports)
SYNOVIAL CYST ( 11 FDA reports)
CATHETER REMOVAL ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CONFUSIONAL STATE ( 10 FDA reports)
HAEMORRHAGE ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
ASCITES ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
FEAR ( 9 FDA reports)
PAIN IN JAW ( 9 FDA reports)
PSEUDOMONAS INFECTION ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
SINUS TACHYCARDIA ( 9 FDA reports)
STRESS ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
COAGULOPATHY ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
ACUTE SINUSITIS ( 7 FDA reports)
AGITATION ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
SOFT TISSUE INFECTION ( 7 FDA reports)
SOFT TISSUE INFLAMMATION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD CULTURE POSITIVE ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
FALL ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
COMA ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
ESCHERICHIA BACTERAEMIA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PORTAL HYPERTENSION ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VARICES OESOPHAGEAL ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
CYSTIC FIBROSIS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPOPERFUSION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARBON DIOXIDE DECREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEVICE INTERACTION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL HEART RATE DECREASED ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTENSIVE TRANSFUSION REACTION ( 3 FDA reports)
ILEUS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 3 FDA reports)
MITRAL VALVE DISEASE ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SPUTUM CULTURE POSITIVE ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
VAGINAL CELLULITIS ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENDODONTIC PROCEDURE ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG HERNIA ( 2 FDA reports)
MASS ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
NODULE ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TWIN PREGNANCY ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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