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

DRUG INTERACTION ( 413 FDA reports)
PYREXIA ( 368 FDA reports)
PNEUMONIA ( 296 FDA reports)
PLATELET COUNT DECREASED ( 289 FDA reports)
DRUG INEFFECTIVE ( 283 FDA reports)
FEBRILE NEUTROPENIA ( 239 FDA reports)
DIARRHOEA ( 209 FDA reports)
RENAL IMPAIRMENT ( 208 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 203 FDA reports)
SEPSIS ( 200 FDA reports)
NEUTROPENIA ( 198 FDA reports)
ANAEMIA ( 196 FDA reports)
NAUSEA ( 173 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 170 FDA reports)
HYPOKALAEMIA ( 166 FDA reports)
NEUTROPHIL COUNT DECREASED ( 153 FDA reports)
PLEURAL EFFUSION ( 153 FDA reports)
THROMBOCYTOPENIA ( 150 FDA reports)
RESPIRATORY FAILURE ( 143 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 139 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 131 FDA reports)
DYSPNOEA ( 129 FDA reports)
PANCYTOPENIA ( 129 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 123 FDA reports)
OEDEMA PERIPHERAL ( 121 FDA reports)
INTERSTITIAL LUNG DISEASE ( 120 FDA reports)
MULTI-ORGAN FAILURE ( 116 FDA reports)
LIVER DISORDER ( 113 FDA reports)
DISEASE PROGRESSION ( 112 FDA reports)
RENAL FAILURE ( 112 FDA reports)
RENAL FAILURE ACUTE ( 104 FDA reports)
VOMITING ( 104 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 103 FDA reports)
INFECTION ( 103 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 101 FDA reports)
HYPONATRAEMIA ( 101 FDA reports)
MALAISE ( 101 FDA reports)
CONDITION AGGRAVATED ( 99 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 94 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 91 FDA reports)
NEUROPATHY PERIPHERAL ( 90 FDA reports)
ASPERGILLOSIS ( 86 FDA reports)
CONVULSION ( 86 FDA reports)
RASH ( 86 FDA reports)
FATIGUE ( 83 FDA reports)
HAEMOGLOBIN DECREASED ( 83 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 82 FDA reports)
FUNGAL INFECTION ( 82 FDA reports)
CONSTIPATION ( 81 FDA reports)
HYPOTENSION ( 80 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 78 FDA reports)
SEPTIC SHOCK ( 78 FDA reports)
ABDOMINAL PAIN ( 77 FDA reports)
ASTHENIA ( 74 FDA reports)
BLOOD BILIRUBIN INCREASED ( 73 FDA reports)
MYALGIA ( 73 FDA reports)
DEATH ( 71 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 70 FDA reports)
BLOOD CREATININE INCREASED ( 70 FDA reports)
CARDIAC FAILURE ( 69 FDA reports)
OEDEMA ( 68 FDA reports)
CELLULITIS ( 66 FDA reports)
HYPERTENSION ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 63 FDA reports)
GRAFT VERSUS HOST DISEASE ( 63 FDA reports)
DRUG RESISTANCE ( 62 FDA reports)
RHABDOMYOLYSIS ( 62 FDA reports)
HEADACHE ( 61 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 60 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 59 FDA reports)
HERPES ZOSTER ( 59 FDA reports)
ILEUS PARALYTIC ( 59 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 59 FDA reports)
STAPHYLOCOCCAL INFECTION ( 59 FDA reports)
TREMOR ( 59 FDA reports)
DECREASED APPETITE ( 56 FDA reports)
DRUG LEVEL INCREASED ( 55 FDA reports)
HAEMOPTYSIS ( 54 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 53 FDA reports)
HEPATIC FAILURE ( 53 FDA reports)
COUGH ( 52 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 51 FDA reports)
BONE MARROW FAILURE ( 51 FDA reports)
MYOPATHY ( 51 FDA reports)
STOMATITIS ( 51 FDA reports)
ASCITES ( 50 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 50 FDA reports)
PAIN ( 50 FDA reports)
URINARY TRACT INFECTION ( 49 FDA reports)
CEREBRAL HAEMORRHAGE ( 48 FDA reports)
DIZZINESS ( 48 FDA reports)
MUSCULAR WEAKNESS ( 48 FDA reports)
PRURITUS ( 48 FDA reports)
HAEMOLYTIC ANAEMIA ( 47 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 46 FDA reports)
UVEITIS ( 46 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 46 FDA reports)
DEHYDRATION ( 45 FDA reports)
BRADYCARDIA ( 44 FDA reports)
NEUTROPENIC SEPSIS ( 44 FDA reports)
ARTHRALGIA ( 43 FDA reports)
WEIGHT INCREASED ( 43 FDA reports)
ATRIAL FIBRILLATION ( 42 FDA reports)
HYPERKALAEMIA ( 42 FDA reports)
LEUKOPENIA ( 42 FDA reports)
SYNCOPE ( 42 FDA reports)
ABDOMINAL DISTENSION ( 41 FDA reports)
CONFUSIONAL STATE ( 41 FDA reports)
HYPERGLYCAEMIA ( 41 FDA reports)
PARAESTHESIA ( 41 FDA reports)
PAIN IN EXTREMITY ( 40 FDA reports)
RENAL DISORDER ( 40 FDA reports)
BLOOD PRESSURE DECREASED ( 39 FDA reports)
CARDIO-RESPIRATORY ARREST ( 39 FDA reports)
FALL ( 39 FDA reports)
JAUNDICE ( 39 FDA reports)
LUNG INFILTRATION ( 39 FDA reports)
LYMPHADENOPATHY ( 39 FDA reports)
BLOOD UREA INCREASED ( 38 FDA reports)
CARDIAC ARREST ( 38 FDA reports)
ERYTHEMA ( 38 FDA reports)
HYPOAESTHESIA ( 38 FDA reports)
LOSS OF CONSCIOUSNESS ( 38 FDA reports)
NEUROTOXICITY ( 38 FDA reports)
PULMONARY OEDEMA ( 38 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 37 FDA reports)
HYPOALBUMINAEMIA ( 37 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 36 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 36 FDA reports)
DRUG ERUPTION ( 36 FDA reports)
HYPERBILIRUBINAEMIA ( 36 FDA reports)
PULMONARY HAEMORRHAGE ( 36 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 36 FDA reports)
WEIGHT DECREASED ( 36 FDA reports)
ASPERGILLOMA ( 35 FDA reports)
CANDIDIASIS ( 35 FDA reports)
GENERALISED OEDEMA ( 35 FDA reports)
HAEMORRHAGE ( 35 FDA reports)
GAIT DISTURBANCE ( 34 FDA reports)
LUNG DISORDER ( 34 FDA reports)
PSEUDOMONAS INFECTION ( 34 FDA reports)
ALOPECIA ( 33 FDA reports)
CYSTITIS HAEMORRHAGIC ( 33 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 33 FDA reports)
GLAUCOMA ( 33 FDA reports)
HEPATIC ENZYME INCREASED ( 33 FDA reports)
MUCOSAL INFLAMMATION ( 33 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 33 FDA reports)
HALLUCINATION ( 32 FDA reports)
LUNG INFECTION ( 32 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
PULMONARY EMBOLISM ( 32 FDA reports)
SOMNOLENCE ( 32 FDA reports)
TREATMENT NONCOMPLIANCE ( 32 FDA reports)
CHILLS ( 31 FDA reports)
DRUG TOXICITY ( 31 FDA reports)
HYPOXIA ( 31 FDA reports)
NO THERAPEUTIC RESPONSE ( 31 FDA reports)
PNEUMONIA BACTERIAL ( 31 FDA reports)
TRANSPLANT REJECTION ( 31 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 30 FDA reports)
BLOOD GLUCOSE INCREASED ( 30 FDA reports)
CARDIOMEGALY ( 30 FDA reports)
CHEST PAIN ( 30 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 30 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 30 FDA reports)
MULTIPLE MYELOMA ( 30 FDA reports)
PERICARDIAL EFFUSION ( 30 FDA reports)
ABASIA ( 29 FDA reports)
ABDOMINAL PAIN UPPER ( 29 FDA reports)
BACK PAIN ( 29 FDA reports)
RHEUMATOID ARTHRITIS ( 29 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 28 FDA reports)
ELECTROLYTE IMBALANCE ( 28 FDA reports)
ENCEPHALOPATHY ( 28 FDA reports)
HAEMATURIA ( 28 FDA reports)
HYPOACUSIS ( 28 FDA reports)
METABOLIC ACIDOSIS ( 28 FDA reports)
APLASTIC ANAEMIA ( 27 FDA reports)
ATELECTASIS ( 27 FDA reports)
INFLAMMATION ( 27 FDA reports)
PHOTOPHOBIA ( 27 FDA reports)
PNEUMONIA FUNGAL ( 27 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 27 FDA reports)
ARRHYTHMIA ( 26 FDA reports)
ASTHMA ( 26 FDA reports)
CHEST DISCOMFORT ( 26 FDA reports)
DEPRESSION ( 26 FDA reports)
PANCREATITIS ( 26 FDA reports)
TUMOUR LYSIS SYNDROME ( 26 FDA reports)
AGRANULOCYTOSIS ( 25 FDA reports)
ANOREXIA ( 25 FDA reports)
DELIRIUM ( 25 FDA reports)
DISEASE RECURRENCE ( 25 FDA reports)
INSOMNIA ( 25 FDA reports)
OLIGURIA ( 25 FDA reports)
OXYGEN SATURATION DECREASED ( 25 FDA reports)
RESPIRATORY DISTRESS ( 25 FDA reports)
SYSTEMIC MYCOSIS ( 25 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
BLOOD ALBUMIN DECREASED ( 24 FDA reports)
CONJUNCTIVITIS ( 24 FDA reports)
EPISTAXIS ( 24 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 24 FDA reports)
ILEUS ( 24 FDA reports)
OSTEONECROSIS ( 24 FDA reports)
TACHYCARDIA ( 24 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 24 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 24 FDA reports)
BLOOD CULTURE POSITIVE ( 23 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 23 FDA reports)
PERICARDITIS ( 23 FDA reports)
PURPURA ( 23 FDA reports)
SINUSITIS ( 23 FDA reports)
UBIQUINONE DECREASED ( 23 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 22 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 22 FDA reports)
BLOOD PRESSURE INCREASED ( 22 FDA reports)
ERYTHEMA MULTIFORME ( 22 FDA reports)
HEPATOTOXICITY ( 22 FDA reports)
HICCUPS ( 22 FDA reports)
HYPERCALCAEMIA ( 22 FDA reports)
HYPOGLYCAEMIA ( 22 FDA reports)
SWELLING FACE ( 22 FDA reports)
THERAPY NON-RESPONDER ( 22 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 21 FDA reports)
ENTEROCOLITIS ( 21 FDA reports)
HAEMODIALYSIS ( 21 FDA reports)
HEPATITIS ( 21 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 21 FDA reports)
PNEUMOTHORAX ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 20 FDA reports)
ENTEROCOCCAL INFECTION ( 20 FDA reports)
HISTOPLASMOSIS ( 20 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 20 FDA reports)
AGITATION ( 19 FDA reports)
BACTERIAL INFECTION ( 19 FDA reports)
BRONCHITIS ( 19 FDA reports)
ENGRAFT FAILURE ( 19 FDA reports)
FLUID OVERLOAD ( 19 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 19 FDA reports)
HYPERHIDROSIS ( 19 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
MOBILITY DECREASED ( 19 FDA reports)
MYOSITIS ( 19 FDA reports)
PALPITATIONS ( 19 FDA reports)
PANCREATITIS ACUTE ( 19 FDA reports)
PNEUMONIA ASPIRATION ( 19 FDA reports)
PRODUCTIVE COUGH ( 19 FDA reports)
PSEUDOMONAL SEPSIS ( 19 FDA reports)
PULMONARY MYCOSIS ( 19 FDA reports)
SHOCK ( 19 FDA reports)
SHOCK HAEMORRHAGIC ( 19 FDA reports)
STEM CELL TRANSPLANT ( 19 FDA reports)
ADRENAL INSUFFICIENCY ( 18 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 18 FDA reports)
BLOOD POTASSIUM DECREASED ( 18 FDA reports)
INJURY ( 18 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 18 FDA reports)
MYELODYSPLASTIC SYNDROME ( 18 FDA reports)
NEOPLASM MALIGNANT ( 18 FDA reports)
PETECHIAE ( 18 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 18 FDA reports)
RESPIRATORY DISORDER ( 18 FDA reports)
RESPIRATORY TRACT INFECTION ( 18 FDA reports)
TRANSPLANT FAILURE ( 18 FDA reports)
VERTIGO ( 18 FDA reports)
ABORTION SPONTANEOUS ( 17 FDA reports)
BLOOD AMYLASE INCREASED ( 17 FDA reports)
CHOLESTASIS ( 17 FDA reports)
CLOSTRIDIAL INFECTION ( 17 FDA reports)
CUSHING'S SYNDROME ( 17 FDA reports)
DIABETES MELLITUS ( 17 FDA reports)
DRUG INTOLERANCE ( 17 FDA reports)
HYPOMAGNESAEMIA ( 17 FDA reports)
SKIN ULCER ( 17 FDA reports)
TORSADE DE POINTES ( 17 FDA reports)
VISION BLURRED ( 17 FDA reports)
VISUAL IMPAIRMENT ( 17 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 16 FDA reports)
BLOOD POTASSIUM INCREASED ( 16 FDA reports)
BLOOD URIC ACID INCREASED ( 16 FDA reports)
BRONCHOPNEUMONIA ( 16 FDA reports)
CEREBRAL INFARCTION ( 16 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 16 FDA reports)
DIALYSIS ( 16 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 16 FDA reports)
EYE PAIN ( 16 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 16 FDA reports)
FUNGAL SEPSIS ( 16 FDA reports)
HAEMATOCRIT DECREASED ( 16 FDA reports)
HYPERLIPIDAEMIA ( 16 FDA reports)
HYPERSENSITIVITY ( 16 FDA reports)
IRON DEFICIENCY ANAEMIA ( 16 FDA reports)
MALNUTRITION ( 16 FDA reports)
PULMONARY CONGESTION ( 16 FDA reports)
TRICHOSPORON INFECTION ( 16 FDA reports)
VASCULITIS ( 16 FDA reports)
ABNORMAL BEHAVIOUR ( 15 FDA reports)
AMNESIA ( 15 FDA reports)
BRAIN OEDEMA ( 15 FDA reports)
BRONCHIECTASIS ( 15 FDA reports)
COAGULOPATHY ( 15 FDA reports)
DYSGEUSIA ( 15 FDA reports)
ENDOPHTHALMITIS ( 15 FDA reports)
EYELID OEDEMA ( 15 FDA reports)
FUNGAL ENDOCARDITIS ( 15 FDA reports)
GASTRIC ULCER ( 15 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 15 FDA reports)
GASTROINTESTINAL DISORDER ( 15 FDA reports)
KERATITIS FUNGAL ( 15 FDA reports)
LEUKOENCEPHALOPATHY ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
PROTEINURIA ( 15 FDA reports)
URINE OUTPUT DECREASED ( 15 FDA reports)
ANXIETY ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CEREBRAL ASPERGILLOSIS ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
EAR DISCOMFORT ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
FLUID RETENTION ( 14 FDA reports)
HERPES SIMPLEX ( 14 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 14 FDA reports)
HYPOVOLAEMIA ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
PANCREATITIS NECROTISING ( 14 FDA reports)
PROTEIN TOTAL DECREASED ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
SPLENOMEGALY ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
TOXIC NEUROPATHY ( 14 FDA reports)
UNRESPONSIVE TO STIMULI ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
VIRAL INFECTION ( 14 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 13 FDA reports)
BACTERAEMIA ( 13 FDA reports)
CARDIAC FAILURE ACUTE ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
DYSURIA ( 13 FDA reports)
EOSINOPHIL COUNT INCREASED ( 13 FDA reports)
GRAND MAL CONVULSION ( 13 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 13 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 13 FDA reports)
MELAENA ( 13 FDA reports)
MUCOUS MEMBRANE DISORDER ( 13 FDA reports)
NOCARDIOSIS ( 13 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 13 FDA reports)
ORGANISING PNEUMONIA ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
STATUS EPILEPTICUS ( 13 FDA reports)
SUBDURAL HAEMATOMA ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
BACTERIAL SEPSIS ( 12 FDA reports)
BODY TEMPERATURE INCREASED ( 12 FDA reports)
COMA ( 12 FDA reports)
CUSHINGOID ( 12 FDA reports)
DIZZINESS POSTURAL ( 12 FDA reports)
DRUG EFFECT DECREASED ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
DYSSTASIA ( 12 FDA reports)
ENTEROCOCCAL SEPSIS ( 12 FDA reports)
EYE INFECTION FUNGAL ( 12 FDA reports)
GASTROENTERITIS ( 12 FDA reports)
HAEMATEMESIS ( 12 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 12 FDA reports)
HYPOPROTEINAEMIA ( 12 FDA reports)
INCONTINENCE ( 12 FDA reports)
JOINT SWELLING ( 12 FDA reports)
LYMPHOMA ( 12 FDA reports)
MENTAL STATUS CHANGES ( 12 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
NEPHROPATHY TOXIC ( 12 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 12 FDA reports)
OCULAR HYPERAEMIA ( 12 FDA reports)
ORAL HERPES ( 12 FDA reports)
PHARYNGITIS ( 12 FDA reports)
POST PROCEDURAL COMPLICATION ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
SKIN EXFOLIATION ( 12 FDA reports)
SKIN INFECTION ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
TREATMENT FAILURE ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
ZYGOMYCOSIS ( 12 FDA reports)
ABNORMAL FAECES ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ANTITHROMBIN III DECREASED ( 11 FDA reports)
BLISTER ( 11 FDA reports)
BLOOD CALCIUM DECREASED ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 11 FDA reports)
CAPILLARY LEAK SYNDROME ( 11 FDA reports)
CHOLANGITIS ( 11 FDA reports)
COLLAPSE OF LUNG ( 11 FDA reports)
COORDINATION ABNORMAL ( 11 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 11 FDA reports)
DEVICE RELATED INFECTION ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
FUNGAEMIA ( 11 FDA reports)
GASTRITIS ( 11 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 11 FDA reports)
HYPOCALCAEMIA ( 11 FDA reports)
INFUSION RELATED REACTION ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
MITRAL VALVE INCOMPETENCE ( 11 FDA reports)
MUSCLE ATROPHY ( 11 FDA reports)
NEOPLASM PROGRESSION ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
NEUROLOGICAL SYMPTOM ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
PLEURISY ( 11 FDA reports)
PSYCHIATRIC SYMPTOM ( 11 FDA reports)
RASH MACULO-PAPULAR ( 11 FDA reports)
SEPTIC EMBOLUS ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SINUS BRADYCARDIA ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
VISUAL ACUITY REDUCED ( 11 FDA reports)
ABDOMINAL DISCOMFORT ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
ANHEDONIA ( 10 FDA reports)
BILE DUCT STONE ( 10 FDA reports)
BK VIRUS INFECTION ( 10 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 10 FDA reports)
BLOOD CHLORIDE DECREASED ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
CHROMATURIA ( 10 FDA reports)
DEAFNESS ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
DRUG DOSE OMISSION ( 10 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
EMOTIONAL DISTRESS ( 10 FDA reports)
ESCHERICHIA SEPSIS ( 10 FDA reports)
EYE INFECTION ( 10 FDA reports)
FAECAL INCONTINENCE ( 10 FDA reports)
HEPATIC MASS ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 10 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 10 FDA reports)
IMMUNOSUPPRESSION ( 10 FDA reports)
INGUINAL HERNIA ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
LOCALISED OEDEMA ( 10 FDA reports)
LYMPHOPENIA ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MOVEMENT DISORDER ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
NEUROGENIC BLADDER ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
OSTEOMYELITIS ( 10 FDA reports)
OVERDOSE ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PNEUMATOSIS INTESTINALIS ( 10 FDA reports)
PROTHROMBIN TIME PROLONGED ( 10 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 10 FDA reports)
PULMONARY INFARCTION ( 10 FDA reports)
REPERFUSION ARRHYTHMIA ( 10 FDA reports)
SCAR ( 10 FDA reports)
SCEDOSPORIUM INFECTION ( 10 FDA reports)
SCOTOMA ( 10 FDA reports)
SKIN BURNING SENSATION ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
VENOOCCLUSIVE DISEASE ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
VISUAL FIELD DEFECT ( 10 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 10 FDA reports)
ADENOVIRUS INFECTION ( 9 FDA reports)
ADRENAL SUPPRESSION ( 9 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
ASPERGILLUS TEST POSITIVE ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BRAIN ABSCESS ( 9 FDA reports)
CANDIDA PNEUMONIA ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CASTLEMAN'S DISEASE ( 9 FDA reports)
CATHETER RELATED INFECTION ( 9 FDA reports)
DEMENTIA ( 9 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
EMBOLISM ( 9 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ( 9 FDA reports)
EPILEPSY ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
IRIS ADHESIONS ( 9 FDA reports)
ISCHAEMIA ( 9 FDA reports)
LIFE EXPECTANCY SHORTENED ( 9 FDA reports)
MASTICATION DISORDER ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
NEURALGIA ( 9 FDA reports)
PERICARDITIS FUNGAL ( 9 FDA reports)
PHLEBOLITH ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 9 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 9 FDA reports)
PULMONARY CAVITATION ( 9 FDA reports)
ROAD TRAFFIC ACCIDENT ( 9 FDA reports)
SCLERITIS ( 9 FDA reports)
STRESS ( 9 FDA reports)
SYSTEMIC CANDIDA ( 9 FDA reports)
TACHYPNOEA ( 9 FDA reports)
ACIDOSIS ( 8 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 8 FDA reports)
BLAST CELL COUNT INCREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
CARDIAC VALVE VEGETATION ( 8 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
CYSTITIS VIRAL ( 8 FDA reports)
DENTAL CARIES ( 8 FDA reports)
DRUG LEVEL DECREASED ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
HAEMORRHAGIC DIATHESIS ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
HIV INFECTION ( 8 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPOCOAGULABLE STATE ( 8 FDA reports)
IMMUNE SYSTEM DISORDER ( 8 FDA reports)
INTESTINAL INFARCTION ( 8 FDA reports)
LEUKAEMIA RECURRENT ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
LOBAR PNEUMONIA ( 8 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
LUNG CONSOLIDATION ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
MOUTH HAEMORRHAGE ( 8 FDA reports)
MYELITIS ( 8 FDA reports)
NEUROPATHY ( 8 FDA reports)
ORAL INTAKE REDUCED ( 8 FDA reports)
OROPHARYNGEAL PAIN ( 8 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 8 FDA reports)
PARADOXICAL DRUG REACTION ( 8 FDA reports)
PHAEHYPHOMYCOSIS ( 8 FDA reports)
PHLEBITIS ( 8 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 8 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 8 FDA reports)
PRIMARY SEQUESTRUM ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RESPIRATORY RATE DECREASED ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SPUTUM CULTURE POSITIVE ( 8 FDA reports)
SUBILEUS ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
SUTURE RUPTURE ( 8 FDA reports)
SWELLING ( 8 FDA reports)
TOOTH FRACTURE ( 8 FDA reports)
UNDERDOSE ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 7 FDA reports)
ANURIA ( 7 FDA reports)
ATRIAL FLUTTER ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 7 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 7 FDA reports)
BLOOD CORTISOL DECREASED ( 7 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 7 FDA reports)
CANDIDA ENDOPHTHALMITIS ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DERMATITIS ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
ESCHERICHIA BACTERAEMIA ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
FUNGAL SKIN INFECTION ( 7 FDA reports)
FUNGUS CULTURE POSITIVE ( 7 FDA reports)
FUSARIUM INFECTION ( 7 FDA reports)
GENERALISED ERYTHEMA ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HEPATOSPLENOMEGALY ( 7 FDA reports)
HYPERAMMONAEMIA ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LUNG ABSCESS ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUCORMYCOSIS ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
NECROSIS ( 7 FDA reports)
NECROTISING FASCIITIS ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PULMONARY GRANULOMA ( 7 FDA reports)
PURULENT DISCHARGE ( 7 FDA reports)
RALES ( 7 FDA reports)
RASH PRURITIC ( 7 FDA reports)
RETINOIC ACID SYNDROME ( 7 FDA reports)
SUBCUTANEOUS ABSCESS ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
ALTERNARIA INFECTION ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 6 FDA reports)
CENTRAL LINE INFECTION ( 6 FDA reports)
CEREBELLAR HAEMORRHAGE ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
COLITIS ( 6 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
DERMATITIS EXFOLIATIVE ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DRUG PRESCRIBING ERROR ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
ENDOCARDITIS BACTERIAL ( 6 FDA reports)
ENTERITIS INFECTIOUS ( 6 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 6 FDA reports)
ERYTHEMA NODOSUM ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FOETAL DISORDER ( 6 FDA reports)
GASTRIC CANCER ( 6 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 6 FDA reports)
GRIP STRENGTH DECREASED ( 6 FDA reports)
GROWTH RETARDATION ( 6 FDA reports)
HEPATIC CYST ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
HYPERPLASIA ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
LUNG NEOPLASM ( 6 FDA reports)
LUNG TRANSPLANT REJECTION ( 6 FDA reports)
MENINGITIS ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 6 FDA reports)
NEOPLASM ( 6 FDA reports)
NEUTROPENIC INFECTION ( 6 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 6 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 6 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
PULMONARY TOXICITY ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RELAPSING FEVER ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 6 FDA reports)
RIGHT VENTRICULAR FAILURE ( 6 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 6 FDA reports)
SJOGREN'S SYNDROME ( 6 FDA reports)
SKIN NECROSIS ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
TOOTHACHE ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
ULCER ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 5 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
ALVEOLAR PROTEINOSIS ( 5 FDA reports)
APHTHOUS STOMATITIS ( 5 FDA reports)
BACTERIA STOOL IDENTIFIED ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD UREA DECREASED ( 5 FDA reports)
BONE MARROW TRANSPLANT ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CHOLESTATIC LIVER INJURY ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
CLOSTRIDIUM COLITIS ( 5 FDA reports)
COMA HEPATIC ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 5 FDA reports)
DEAFNESS NEUROSENSORY ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DRUG-INDUCED LIVER INJURY ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ENCEPHALITIS HERPES ( 5 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 5 FDA reports)
FISTULA ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HEPATOBILIARY DISEASE ( 5 FDA reports)
HERPES DERMATITIS ( 5 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 5 FDA reports)
HYDROTHORAX ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
LEFT ATRIAL DILATATION ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LOOSE TOOTH ( 5 FDA reports)
LYMPHATIC DUCT RUPTURE ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MULTIPLE SCLEROSIS ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
OSTEOLYSIS ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PANCREATIC DISORDER ( 5 FDA reports)
PARALYSIS ( 5 FDA reports)
PARAPLEGIA ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
SPINAL FRACTURE ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
SPLENIC INFARCTION ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STENOTROPHOMONAS INFECTION ( 5 FDA reports)
SUBDURAL HAEMORRHAGE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
ULCERATIVE KERATITIS ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
VACCINATION COMPLICATION ( 5 FDA reports)
VANISHING BILE DUCT SYNDROME ( 5 FDA reports)
VARICELLA ( 5 FDA reports)
VASCULAR PURPURA ( 5 FDA reports)
XANTHOPSIA ( 5 FDA reports)
ACNE ( 4 FDA reports)
ACTINIC KERATOSIS ( 4 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHERESIS ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ASPIRATION BONE MARROW ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
BACTERIAL CULTURE POSITIVE ( 4 FDA reports)
BACTERIAL TEST POSITIVE ( 4 FDA reports)
BIOPSY ( 4 FDA reports)
BLADDER DISORDER ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
BRONCHOSTENOSIS ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CAECITIS ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CARDIOPULMONARY FAILURE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CATHETERISATION VENOUS ( 4 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 4 FDA reports)
CHEYNE-STOKES RESPIRATION ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
COCCIDIOIDOMYCOSIS ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 4 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
CORNEAL PERFORATION ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ENDOCARDITIS CANDIDA ( 4 FDA reports)
ENDOTOXAEMIA ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FEEDING DISORDER ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROINTESTINAL TOXICITY ( 4 FDA reports)
GENITAL HERPES ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HEPATOBLASTOMA RECURRENT ( 4 FDA reports)
HISTOLOGY ABNORMAL ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KERION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MANIA ( 4 FDA reports)
MANTLE CELL LYMPHOMA ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
NEUTROPENIC COLITIS ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 4 FDA reports)
ORAL MUCOSA ATROPHY ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OSTEOSCLEROSIS ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERINEPHRIC ABSCESS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMONIA HERPES VIRAL ( 4 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 4 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
PSEUDOALDOSTERONISM ( 4 FDA reports)
PSEUDOCYST ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RETCHING ( 4 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SICCA SYNDROME ( 4 FDA reports)
SKIN HYPERTROPHY ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN SWELLING ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
STREPTOCOCCAL SEPSIS ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
TENOSYNOVITIS ( 4 FDA reports)
TINEA PEDIS ( 4 FDA reports)
TOOTH RESORPTION ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 4 FDA reports)
URINE ABNORMALITY ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
VITREOUS OPACITIES ( 4 FDA reports)
VOLVULUS ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
ACANTHAMOEBA INFECTION ( 3 FDA reports)
ACETABULUM FRACTURE ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AEROMONA INFECTION ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 3 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBIOTIC LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
AORTIC VALVE SCLEROSIS ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
ASTEATOSIS ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BLOOD TEST ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATHETER SEPSIS ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CERVIX CARCINOMA RECURRENT ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 3 FDA reports)
CORYNEBACTERIUM SEPSIS ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DENTAL OPERATION ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTREMITY CONTRACTURE ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GRAFT DYSFUNCTION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 3 FDA reports)
IIIRD NERVE PARALYSIS ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
IVTH NERVE PARALYSIS ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MENINGITIS FUNGAL ( 3 FDA reports)
MENINGITIS TOXOPLASMAL ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METAPNEUMOVIRUS INFECTION ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MUCOSAL NECROSIS ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYELOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
ORAL INFECTION ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OVARIAN ATROPHY ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
PRODUCT CONTAINER ISSUE ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PYOMETRA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RASH VESICULAR ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RENAL VEIN THROMBOSIS ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SPOROTRICHOSIS ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THYROID ATROPHY ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URETERIC RUPTURE ( 3 FDA reports)
URINARY CASTS ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VIRUS URINE TEST POSITIVE ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
XERODERMA ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACANTHAMOEBA KERATITIS ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTHRITIS FUNGAL ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BACTERIA URINE IDENTIFIED ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BILE DUCT NECROSIS ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD CALCIUM ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHITIS FUNGAL ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CEREBRAL ATROPHY CONGENITAL ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
CORNEAL THINNING ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CSF GLUCOSE INCREASED ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYTARABINE SYNDROME ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DACRYOCANALICULITIS ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
EAR MALFORMATION ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
HAEMOPERFUSION ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS INFECTIOUS ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFANTILE SPITTING UP ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL ADENOCARCINOMA ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
IRIDECTOMY ( 2 FDA reports)
IRIS OPERATION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 2 FDA reports)
LEUKOSTASIS ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
MASS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MECONIUM STAIN ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MINERAL DEFICIENCY ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE NECROSIS ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL NECROSIS ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PARACOCCIDIOIDES INFECTION ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PENICILLIOSIS ( 2 FDA reports)
PENILE SIZE REDUCED ( 2 FDA reports)
PERIORBITAL ABSCESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PITYRIASIS ( 2 FDA reports)
PLASMINOGEN DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURAL RUB ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
PYURIA ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RETINAL INFILTRATES ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
RHEUMATOID FACTOR INCREASED ( 2 FDA reports)
SCAB ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THYROID CANCER ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRISOMY 18 ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTI-THYROID ANTIBODY ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CD4 LYMPHOCYTES ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBELLOPONTINE ANGLE TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUTTERING ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS MUCOCUTANEOUS ULCER ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCEPHALITIS POST MEASLES ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPOSURE TO CONTAMINATED DEVICE ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HLA MARKER STUDY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE INTESTINE OPERATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEIOMYOMA ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG INFILTRATION MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROSPORUM INFECTION ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE ENZYME DECREASED ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NECROTISING SCLERITIS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE STIMULATION TEST NORMAL ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DESTRUCTION INCREASED ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIOVENOUS FISTULA ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULMONARY VASCULITIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHEUMATOID FACTOR QUANTITATIVE INCREASED ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SERRATIA BACTERAEMIA ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPINAL DECOMPRESSION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SYMPATHETIC NERVE INJURY ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THORACIC OPERATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRICHOPHYTIC GRANULOMA ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYPHUS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRELATED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)