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
125884991 12588499 1 I 20160629 20160701 20160725 20160725 PER US-JNJFOC-20160702738 JANSSEN 79.00 YR E F Y 88.45000 KG 20160725 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
125884991 12588499 1 PS TYLENOL 8 HR ARTHRITIS PAIN ACETAMINOPHEN 1 Oral U U 1390892 19872 TABLET
125884991 12588499 2 SS TYLENOL 8 HR ARTHRITIS PAIN ACETAMINOPHEN 1 Oral U U 1390892 19872 1 DF TABLET QD
125884991 12588499 3 C COUMADIN WARFARIN SODIUM 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125884991 12588499 2 Arthritis
125884991 12588499 3 Anticoagulant therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125884991 12588499 Abdominal pain upper
125884991 12588499 Contraindicated product administered
125884991 12588499 Dyspepsia
125884991 12588499 Incorrect dose administered

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
125884991 12588499 2 20160629 0