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
125685041 12568504 1 I 20160706 20160719 20160719 EXP CA-JNJFOC-20160710599 JOHNSON AND JOHNSON 19.00 YR A F Y 0.00000 20160718 PH CA CA

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
125685041 12568504 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 UNSPECIFIED
125685041 12568504 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U U 19872 7.5 G UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125685041 12568504 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125685041 12568504 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125685041 12568504 Aspartate aminotransferase increased
125685041 12568504 Blood bilirubin increased
125685041 12568504 Intentional overdose
125685041 12568504 International normalised ratio increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found