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
125759351 12575935 1 I 20160706 20160720 20160720 EXP CA-JNJFOC-20160710643 JOHNSON AND JOHNSON 36.00 YR A F Y 0.00000 20160720 MD 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
125759351 12575935 1 PS TYLENOL ACETAMINOPHEN 1 Oral U U 19872 TABLET
125759351 12575935 2 SS TYLENOL ACETAMINOPHEN 1 Oral FOR 3 DAYS U U 19872 30 DF TABLET
125759351 12575935 3 SS LYRICA PREGABALIN 1 Oral U 0 300 MG CAPSULE
125759351 12575935 4 C NAPROXEN. NAPROXEN 1 Unknown 0 UNSPECIFIED
125759351 12575935 5 C DEMEROL MEPERIDINE HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125759351 12575935 2 Product used for unknown indication
125759351 12575935 3 Product used for unknown indication
125759351 12575935 4 Product used for unknown indication
125759351 12575935 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125759351 12575935 HO
125759351 12575935 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125759351 12575935 Hepatic failure
125759351 12575935 Intentional product misuse
125759351 12575935 Overdose

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

no results found

Therapies reported

no results found