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

CEREBRAL INFARCTION ( 18 FDA reports)
PNEUMONIA ( 16 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
CONVULSION ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
MALAISE ( 9 FDA reports)
OSTEOMYELITIS ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 8 FDA reports)
STERNAL FRACTURE ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
PSEUDARTHROSIS ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
FALL ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
LYMPHATIC DUCT RUPTURE ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MENINGITIS TUBERCULOUS ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COUGH ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
COXSACKIE VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TETANY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)

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