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
123574793 12357479 3 F 20160412 20160718 20160511 20160727 EXP US-JNJFOC-20160505687 JOHNSON AND JOHNSON 29.39 YR A M 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
123574793 12357479 1 PS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown Y N 19872 UNSPECIFIED
123574793 12357479 2 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown QUARTERLY 4 HOURS X 1 WEEK Y N 19872 1500 MG UNSPECIFIED
123574793 12357479 3 SS VICKS DAYQUIL DEXTROMETHORPHAN HYDROBROMIDEGUAIFENESIN 1 Unknown INTERMITTENTLY OVER SAME TIME PERIOD U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123574793 12357479 2 Myalgia
123574793 12357479 3 Respiratory symptom

Outcome of event

Event ID CASEID OUTC COD
123574793 12357479 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123574793 12357479 Overdose
123574793 12357479 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
123574793 12357479 2 20160412 201604 0