Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125710921 | 12571092 | 1 | I | 20160713 | 20160719 | 20160719 | EXP | BR-SA-2016SA130142 | AVENTIS | FREIRE PS, MONTONI JD, RIBEIRO ASM, MARQUES HH, MAUAD T, SILVA CA. MILIARY TUBERCULOSIS: A SEVERE OPPORTUNISTIC INFECTION IN JUVENILE SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS. REV BRAS REUMATOL. 2016;56(3):274-9. AVAILABLE FROM: HTTP://DX.DOI.ORG/10.1016/J.RBRE.2014.04.007. ACCESSED ON: 2014 NOV 28. | 20.00 | YR | A | F | Y | 0.00000 | 20160719 | OT | BR | BR |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125710921 | 12571092 | 1 | SS | PREDNISONE. | PREDNISONE | 1 | Intravenous (not otherwise specified) | U | UNK | 0 | 60 | MG | QD | ||||||
125710921 | 12571092 | 2 | PS | CHLOROQUINE PHOSPHATE. | CHLOROQUINE PHOSPHATE | 1 | Unknown | U | UNK | 6002 | 250 | MG | QD | ||||||
125710921 | 12571092 | 3 | SS | METHYLPREDNISOLONE HYDROGEN SUCCINATE | METHYLPREDNISOLONE HEMISUCCINATE | 1 | Unknown | U | UNK | 0 | 1 | G | QD | ||||||
125710921 | 12571092 | 4 | SS | AZATHIOPRINE. | AZATHIOPRINE | 1 | Unknown | U | UNK | 0 | 100 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125710921 | 12571092 | 1 | Systemic lupus erythematosus |
125710921 | 12571092 | 2 | Systemic lupus erythematosus |
125710921 | 12571092 | 3 | Systemic lupus erythematosus |
125710921 | 12571092 | 4 | Systemic lupus erythematosus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125710921 | 12571092 | HO |
125710921 | 12571092 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125710921 | 12571092 | Abdominal pain | |
125710921 | 12571092 | Brain herniation | |
125710921 | 12571092 | Coma | |
125710921 | 12571092 | Coma scale abnormal | |
125710921 | 12571092 | Disseminated tuberculosis | |
125710921 | 12571092 | Granulomatous liver disease | |
125710921 | 12571092 | Hepatic necrosis | |
125710921 | 12571092 | Lung infiltration | |
125710921 | 12571092 | Papilloedema | |
125710921 | 12571092 | Peritonitis | |
125710921 | 12571092 | Pneumonia | |
125710921 | 12571092 | Pyrexia | |
125710921 | 12571092 | Sepsis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |