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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123516813 | 12351681 | 3 | F | 20160503 | 20160920 | 20160510 | 20160927 | EXP | US-JNJFOC-20160505175 | JOHNSON AND JOHNSON | 45.98 | YR | A | M | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123516813 | 12351681 | 1 | PS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | Y | N | 19872 | UNSPECIFIED | ||||||||
| 123516813 | 12351681 | 2 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | 7.5 G PER DAY FOR 3 DAYS. | Y | N | 19872 | 7.5 | G | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123516813 | 12351681 | 2 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123516813 | 12351681 | HO |
| 123516813 | 12351681 | LT |
| 123516813 | 12351681 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123516813 | 12351681 | Abdominal pain | |
| 123516813 | 12351681 | Hepatic encephalopathy | |
| 123516813 | 12351681 | Hepatic failure | |
| 123516813 | 12351681 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |