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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125994411 | 12599441 | 1 | I | 20160718 | 20160727 | 20160727 | EXP | US-PERRIGO-16US018144 | PERRIGO | 62.00 | YR | M | Y | 0.00000 | 20160727 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125994411 | 12599441 | 1 | PS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | U | UNKNOWN | 75077 | MODIFIED-RELEASE TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125994411 | 12599441 | 1 | Back pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125994411 | 12599441 | HO |
| 125994411 | 12599441 | DE |
| 125994411 | 12599441 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125994411 | 12599441 | Cardiac arrest | |
| 125994411 | 12599441 | Cardio-respiratory arrest | |
| 125994411 | 12599441 | Hepatic failure | |
| 125994411 | 12599441 | Intentional product misuse | |
| 125994411 | 12599441 | Organ failure | |
| 125994411 | 12599441 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |