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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 886279712 | 8862797 | 12 | F | 201002 | 20160812 | 20121026 | 20160823 | EXP | US-JNJFOC-20121012206 | JOHNSON AND JOHNSON | 37.86 | YR | A | F | Y | 59.00000 | KG | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 886279712 | 8862797 | 1 | SS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | 1000MG AT 2 AM AND 3000MG AT 5 AM | U | U | 0 | 4000 | MG | TABLET | |||||
| 886279712 | 8862797 | 2 | PS | TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | 1 | Oral | 1000MG AT 2 PM AND 1000MG AT 10PM. | U | U | 19872 | 1000 | MG | TABLET | BID | ||||
| 886279712 | 8862797 | 3 | SS | MOTRIN | IBUPROFEN | 1 | Unknown | U | U | 17463 | UNSPECIFIED | ||||||||
| 886279712 | 8862797 | 4 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | Y | 0 | UNSPECIFIED | |||||||||
| 886279712 | 8862797 | 5 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 0 | 25 | MG | PROLONGED-RELEASE TABLET | QD | |||||||
| 886279712 | 8862797 | 6 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 0 | 50 | MG | PROLONGED-RELEASE TABLET | QD | |||||||
| 886279712 | 8862797 | 7 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 0 | 50 | MG | PROLONGED-RELEASE TABLET | QD | |||||||
| 886279712 | 8862797 | 8 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 0 | 25 | MG | PROLONGED-RELEASE TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 886279712 | 8862797 | 1 | Toothache |
| 886279712 | 8862797 | 2 | Toothache |
| 886279712 | 8862797 | 3 | Product used for unknown indication |
| 886279712 | 8862797 | 4 | Toothache |
| 886279712 | 8862797 | 5 | Depression |
| 886279712 | 8862797 | 6 | Depression |
| 886279712 | 8862797 | 7 | Anxiety |
| 886279712 | 8862797 | 8 | Anxiety |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 886279712 | 8862797 | OT |
| 886279712 | 8862797 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 886279712 | 8862797 | Accidental overdose | |
| 886279712 | 8862797 | Acute hepatic failure | |
| 886279712 | 8862797 | Acute kidney injury | |
| 886279712 | 8862797 | Hepatotoxicity | |
| 886279712 | 8862797 | Hypotension |
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 |
|---|---|---|---|---|---|---|
| 886279712 | 8862797 | 2 | 20100223 | 0 | ||
| 886279712 | 8862797 | 4 | 20100224 | 20100227 | 0 | |
| 886279712 | 8862797 | 5 | 20120925 | 20121001 | 0 | |
| 886279712 | 8862797 | 6 | 20121002 | 20130402 | 0 | |
| 886279712 | 8862797 | 7 | 20121002 | 20130402 | 0 | |
| 886279712 | 8862797 | 8 | 20120925 | 20121001 | 0 |