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
917708110 9177081 10 F 201109 20160701 20130321 20160712 EXP US-JNJFOC-20130306621 JOHNSON AND JOHNSON 58.24 YR F Y 90.72000 KG 20160712 CN 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
917708110 9177081 1 PS TYLENOL ACETAMINOPHEN 1 Oral N 19872 UNSPECIFIED
917708110 9177081 2 SS TYLENOL ACETAMINOPHEN 1 Oral N 19872 UNSPECIFIED
917708110 9177081 3 SS TYLENOL PM ACETAMINOPHENDIPHENHYDRAMINE 1 Oral N 0 UNSPECIFIED
917708110 9177081 4 SS TYLENOL PM ACETAMINOPHENDIPHENHYDRAMINE 1 Oral N 999999 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
917708110 9177081 2 Pain
917708110 9177081 3 Sleep disorder therapy
917708110 9177081 4 Pain

Outcome of event

Event ID CASEID OUTC COD
917708110 9177081 HO
917708110 9177081 DE
917708110 9177081 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
917708110 9177081 Acute hepatic failure
917708110 9177081 Acute kidney injury
917708110 9177081 Acute respiratory failure
917708110 9177081 Brain oedema
917708110 9177081 Encephalopathy
917708110 9177081 Hyperammonaemia
917708110 9177081 Mental status changes
917708110 9177081 Overdose
917708110 9177081 Toxicity to various agents

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

no results found

Therapies reported

no results found