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
123736693 12373669 3 F 20160427 20160718 20160516 20160727 EXP US-JNJFOC-20160504266 JOHNSON AND JOHNSON 28.27 YR A F Y 0.00000 20160727 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
123736693 12373669 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Oral N 19872 UNSPECIFIED
123736693 12373669 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Oral N 19872 19.5 G UNSPECIFIED
123736693 12373669 3 SS CLONAZEPAM. CLONAZEPAM 1 Oral 0 5 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123736693 12373669 2 Product used for unknown indication
123736693 12373669 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123736693 12373669 HO
123736693 12373669 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123736693 12373669 Abdominal pain
123736693 12373669 Intentional overdose
123736693 12373669 Intentional self-injury
123736693 12373669 International normalised ratio increased
123736693 12373669 Nausea
123736693 12373669 Transaminases increased

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
123736693 12373669 2 20160427 20160427 0
123736693 12373669 3 20160427 20160427 0