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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126168792 | 12616879 | 2 | F | 200010 | 20160720 | 20160802 | 20160804 | EXP | US-JNJFOC-20160719469 | JOHNSON AND JOHNSON | LARSON. ACETAMINOPHEN-INDUCED ACUTE LIVER FAILURE: RESULTS OF A UNITED STATES MULTICENTER, PROSPECTIVE STUDY. HEPATOLOGY 2005. | 62.00 | YR | A | F | Y | 73.00000 | KG | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126168792 | 12616879 | 1 | PS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | U | U | 19872 | UNSPECIFIED | ||||||||
| 126168792 | 12616879 | 2 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | U | U | 19872 | 3000 | MG | UNSPECIFIED | QD | |||||
| 126168792 | 12616879 | 3 | SS | TYLENOL PM | ACETAMINOPHENDIPHENHYDRAMINE | 1 | Unknown | U | U | 999999 | UNSPECIFIED | ||||||||
| 126168792 | 12616879 | 4 | C | PREMARIN | ESTROGENS, CONJUGATED | 1 | Unknown | 0 | 25 | UG | UNSPECIFIED | ||||||||
| 126168792 | 12616879 | 5 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Unknown | 0 | 20 | MG | UNSPECIFIED | ||||||||
| 126168792 | 12616879 | 6 | C | PREVACID | LANSOPRAZOLE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126168792 | 12616879 | 2 | Pain in extremity |
| 126168792 | 12616879 | 3 | Product used for unknown indication |
| 126168792 | 12616879 | 4 | Product used for unknown indication |
| 126168792 | 12616879 | 5 | Product used for unknown indication |
| 126168792 | 12616879 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126168792 | 12616879 | HO |
| 126168792 | 12616879 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126168792 | 12616879 | Acute hepatic failure | |
| 126168792 | 12616879 | Acute kidney injury | |
| 126168792 | 12616879 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 126168792 | 12616879 | 2 | 2000 | 20001005 | 0 | |
| 126168792 | 12616879 | 3 | 2000 | 20001005 | 0 | |
| 126168792 | 12616879 | 4 | 20001004 | 0 | ||
| 126168792 | 12616879 | 5 | 20001004 | 0 | ||
| 126168792 | 12616879 | 6 | 20001005 | 0 |