The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126168782 12616878 2 F 20160720 20160802 20160804 EXP US-JNJFOC-20160719468 JOHNSON AND JOHNSON LARSON AM. ACETAMINOPHEN-INDUCED ACUTE LIVER FAILURE: RESULTS OF A UNITED STATES MULTICENTER, PROSPECTIVE STUDY. HEPATOLOGY 2005. 37.00 YR A F Y 57.00000 KG 20160804 MD 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
126168782 12616878 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
126168782 12616878 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown (TOTAL DOSE 12000 MG) CHRONIC USE 3 DAYS, 4 G FOR 3 DAYS U U 19872 4 G UNSPECIFIED
126168782 12616878 3 C IBUPROFEN. IBUPROFEN 1 Unknown 30 DAYS 0 600 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126168782 12616878 2 Product used for unknown indication
126168782 12616878 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126168782 12616878 OT
126168782 12616878 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126168782 12616878 Acute hepatic failure
126168782 12616878 Overdose

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
126168782 12616878 2 20000413 0
126168782 12616878 3 20000409 0