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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 95206316 | 9520631 | 6 | F | 20101030 | 20160817 | 20130913 | 20160829 | EXP | US-JNJFOC-20130904624 | JOHNSON AND JOHNSON | 25.41 | YR | A | F | Y | 68.04000 | KG | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 95206316 | 9520631 | 1 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | RECOMMENDED DAILY DOSE | N | 0 | UNKNOWN | ||||||||
| 95206316 | 9520631 | 2 | PS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | RECOMMENDED DAILY DOSE | N | 19872 | UNKNOWN | ||||||||
| 95206316 | 9520631 | 3 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Unknown | RECOMMENDED DAILY DOSE | N | 19872 | UNKNOWN | ||||||||
| 95206316 | 9520631 | 4 | SS | TYLENOL REGULAR STRENGTH | ACETAMINOPHEN | 1 | Unknown | N | 19872 | UNSPECIFIED | |||||||||
| 95206316 | 9520631 | 5 | SS | TYLENOL REGULAR STRENGTH | ACETAMINOPHEN | 1 | Unknown | N | 19872 | UNSPECIFIED | |||||||||
| 95206316 | 9520631 | 6 | SS | TYLENOL PM | ACETAMINOPHENDIPHENHYDRAMINE | 1 | Unknown | N | 999999 | UNSPECIFIED | |||||||||
| 95206316 | 9520631 | 7 | SS | TYLENOL EXTRA STRENGTH NIGHTTIME | ACETAMINOPHENDIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | N | 999999 | UNSPECIFIED | |||||||||
| 95206316 | 9520631 | 8 | C | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 95206316 | 9520631 | 9 | C | LORTAB | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 95206316 | 9520631 | 10 | C | SEASONIQUE | ETHINYL ESTRADIOLLEVONORGESTREL | 1 | Oral | LAST TAKEN: 05-MAY-2010 | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 95206316 | 9520631 | 1 | Influenza |
| 95206316 | 9520631 | 2 | Abdominal pain upper |
| 95206316 | 9520631 | 3 | Malaise |
| 95206316 | 9520631 | 5 | Product used for unknown indication |
| 95206316 | 9520631 | 6 | Product used for unknown indication |
| 95206316 | 9520631 | 7 | Product used for unknown indication |
| 95206316 | 9520631 | 8 | Abdominal pain upper |
| 95206316 | 9520631 | 9 | Malaise |
| 95206316 | 9520631 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 95206316 | 9520631 | HO |
| 95206316 | 9520631 | OT |
| 95206316 | 9520631 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 95206316 | 9520631 | Acute hepatic failure | |
| 95206316 | 9520631 | Anaemia | |
| 95206316 | 9520631 | Brain herniation | |
| 95206316 | 9520631 | Brain oedema | |
| 95206316 | 9520631 | Coagulopathy | |
| 95206316 | 9520631 | Hepatic encephalopathy | |
| 95206316 | 9520631 | Hepatic necrosis | |
| 95206316 | 9520631 | Overdose | |
| 95206316 | 9520631 | Respiratory failure | |
| 95206316 | 9520631 | Toxicity to various agents |
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 |
|---|---|---|---|---|---|---|
| 95206316 | 9520631 | 1 | 20100525 | 20100530 | 0 | |
| 95206316 | 9520631 | 2 | 20100525 | 20100530 | 0 | |
| 95206316 | 9520631 | 3 | 20100525 | 20100530 | 0 | |
| 95206316 | 9520631 | 5 | 2010 | 20100601 | 0 | |
| 95206316 | 9520631 | 6 | 2010 | 20100601 | 0 | |
| 95206316 | 9520631 | 7 | 2010 | 20100601 | 0 |