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PNEUMOCYSTIS JIROVECI PNEUMONIA ( 30 FDA reports)
PYREXIA ( 29 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
HERPES ZOSTER ( 13 FDA reports)
TUBERCULOUS PLEURISY ( 13 FDA reports)
INFUSION RELATED REACTION ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
PANCYTOPENIA ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
VOMITING ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
LYMPHOMA ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
DISSEMINATED TUBERCULOSIS ( 9 FDA reports)
INFECTION ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
TUBERCULOSIS ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
BREAST CANCER ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CHILLS ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
DEMYELINATION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
FALL ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LYMPH NODE TUBERCULOSIS ( 5 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 4 FDA reports)
CERVICAL GLAND TUBERCULOSIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CUTANEOUS TUBERCULOSIS ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
LISTERIA ENCEPHALITIS ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
PNEUMONIA HERPES VIRAL ( 4 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 4 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 4 FDA reports)
PURULENT DISCHARGE ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRONCHITIS ACUTE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COUGH ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HUMERUS FRACTURE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
RASH ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PROCTOSTOMY ( 2 FDA reports)
PROPOFOL INFUSION SYNDROME ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PH URINE INCREASED ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)

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