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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125413812 | 12541381 | 2 | F | 20160624 | 20160708 | 20160709 | EXP | US-JNJFOC-20160625901 | JOHNSON AND JOHNSON | 12.00 | YR | C | F | Y | 43.00000 | KG | 20160709 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125413812 | 12541381 | 1 | PS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | AMOUNT OF EXPOSURE 7G.??DURATION WAS }24HOUR{=1 WEEK | U | U | 19872 | 7 | G | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125413812 | 12541381 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125413812 | 12541381 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125413812 | 12541381 | Incorrect dose administered | |
125413812 | 12541381 | Toxicity to various agents | |
125413812 | 12541381 | Transaminases increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |