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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126211113 | 12621111 | 3 | F | 20160912 | 20160804 | 20160916 | PER | US-PFIZER INC-2016372031 | PFIZER | 69.00 | YR | M | Y | 0.00000 | 20160916 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126211113 | 12621111 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 50 MG, 1X/DAY | Y | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | QD | ||||||
| 126211113 | 12621111 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 100 MG, 1X/DAY | Y | 21992 | 100 | MG | PROLONGED-RELEASE TABLET | QD | ||||||
| 126211113 | 12621111 | 3 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 50 MG, UNK | Y | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | |||||||
| 126211113 | 12621111 | 4 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 25 MG, UNK | Y | 21992 | 25 | MG | PROLONGED-RELEASE TABLET | |||||||
| 126211113 | 12621111 | 5 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 50 MG, 1X/DAY | Y | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | QD | ||||||
| 126211113 | 12621111 | 6 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 25 MG, 1X/DAY | Y | 21992 | 25 | MG | PROLONGED-RELEASE TABLET | QD | ||||||
| 126211113 | 12621111 | 7 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | UNK | 0 | |||||||||||
| 126211113 | 12621111 | 8 | C | RAMIPRIL. | RAMIPRIL | 1 | UNK | 0 | |||||||||||
| 126211113 | 12621111 | 9 | C | PRIMIDONE. | PRIMIDONE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126211113 | 12621111 | 1 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126211113 | 12621111 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126211113 | 12621111 | Dizziness | |
| 126211113 | 12621111 | Drug withdrawal syndrome | |
| 126211113 | 12621111 | Fatigue | |
| 126211113 | 12621111 | Feeling abnormal |
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 |
|---|---|---|---|---|---|---|
| 126211113 | 12621111 | 2 | 20160418 | 201605 | 0 | |
| 126211113 | 12621111 | 3 | 201605 | 201606 | 0 | |
| 126211113 | 12621111 | 4 | 20160629 | 0 | ||
| 126211113 | 12621111 | 5 | 20160205 | 0 | ||
| 126211113 | 12621111 | 6 | 20160725 | 0 | ||
| 126211113 | 12621111 | 9 | 20160418 | 0 |