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

PYREXIA ( 62 FDA reports)
RENAL FAILURE ( 60 FDA reports)
NAUSEA ( 49 FDA reports)
VOMITING ( 46 FDA reports)
RENAL FAILURE ACUTE ( 45 FDA reports)
DIARRHOEA ( 40 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 39 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 39 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 39 FDA reports)
THROMBOCYTOPENIA ( 35 FDA reports)
DIZZINESS ( 34 FDA reports)
HYPERLIPIDAEMIA ( 34 FDA reports)
NEUTROPENIA ( 33 FDA reports)
PANCYTOPENIA ( 33 FDA reports)
PNEUMONIA ( 33 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 31 FDA reports)
HYPOKALAEMIA ( 27 FDA reports)
CALCULUS URINARY ( 25 FDA reports)
HIV WASTING SYNDROME ( 25 FDA reports)
DYSPNOEA ( 24 FDA reports)
BLOOD BILIRUBIN INCREASED ( 23 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 23 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 23 FDA reports)
HYPERTENSION ( 23 FDA reports)
FATIGUE ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
MULTI-ORGAN FAILURE ( 19 FDA reports)
RESPIRATORY FAILURE ( 19 FDA reports)
RASH ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
ANAEMIA ( 15 FDA reports)
FEBRILE NEUTROPENIA ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 12 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
PULMONARY EMBOLISM ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASTHENIA ( 11 FDA reports)
BACTERAEMIA ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
MALAISE ( 11 FDA reports)
PANCREATITIS ( 11 FDA reports)
BLOOD AMYLASE INCREASED ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
CYTOLYTIC HEPATITIS ( 10 FDA reports)
DRUG HYPERSENSITIVITY ( 10 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 10 FDA reports)
MUCOSAL INFLAMMATION ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
TACHYCARDIA ( 10 FDA reports)
VENOOCCLUSIVE DISEASE ( 10 FDA reports)
ERYSIPELAS ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 9 FDA reports)
HAEMOPTYSIS ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
RENAL TUBULAR NECROSIS ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
CHILLS ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 8 FDA reports)
NEPHROPATHY TOXIC ( 8 FDA reports)
PATHOGEN RESISTANCE ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
TOXOPLASMOSIS ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ASCITES ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
COR PULMONALE ACUTE ( 7 FDA reports)
COUGH ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
FLUID OVERLOAD ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 6 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
RASH MACULO-PAPULAR ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
T-CELL LYMPHOMA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DRUG RESISTANCE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MASS ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
UVEITIS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
BK VIRUS INFECTION ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
DEATH ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 2 FDA reports)
GEOTRICHUM INFECTION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PACHYMENINGITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCHISTOSOMIASIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL DILATATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTOIMMUNE DEFICIENCY SYNDROME ( 1 FDA reports)
BABESIOSIS ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYSTIC LYMPHANGIOMA ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED VIBRATORY SENSE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PROCTITIS HERPES ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use