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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125884701 | 12588470 | 1 | I | 20160605 | 20160628 | 20160725 | 20160725 | PER | US-JNJFOC-20160626803 | JANSSEN | 81.00 | YR | E | F | Y | 64.86000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125884701 | 12588470 | 1 | PS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | N | 1391670 | 19872 | TABLET | ||||||||
125884701 | 12588470 | 2 | SS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | 2 TABLETS, EVERY 6 HOURS FOR FIRST FEW DAYS, NOW TAKING TWICE A DAY | N | 1391670 | 19872 | 2 | DF | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125884701 | 12588470 | 2 | Analgesic therapy |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125884701 | 12588470 | Inappropriate schedule of drug administration | |
125884701 | 12588470 | Product expiration date issue | |
125884701 | 12588470 | Product lot number issue |
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 |
---|---|---|---|---|---|---|
125884701 | 12588470 | 2 | 20160605 | 0 |