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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126204901 | 12620490 | 1 | I | 200011 | 20160720 | 20160804 | 20160804 | EXP | US-JNJFOC-20160720131 | JOHNSON AND JOHNSON | LARSON. ACETAMINOPHEN-INDUCED ACUTE LIVER FAILURE: RESULTS OF A UNITED STATES MULTICENTER, PROSPECTIVE STUDY. HEPATOLOGY 2005. | 31.00 | YR | A | F | Y | 57.50000 | KG | 20160804 | OT | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126204901 | 12620490 | 1 | PS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | U | U | 19872 | UNSPECIFIED | ||||||||
126204901 | 12620490 | 2 | SS | TYLENOL | ACETAMINOPHEN | 1 | Unknown | 4000 | MG | U | U | 19872 | 1000 | MG | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126204901 | 12620490 | 2 | Malaise |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126204901 | 12620490 | OT |
126204901 | 12620490 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126204901 | 12620490 | Acute hepatic failure | |
126204901 | 12620490 | Off label use | |
126204901 | 12620490 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
126204901 | 12620490 | 2 | 200011 | 20001113 | 0 |