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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105875001 | 10587500 | 1 | I | 20141111 | 20141117 | 20141117 | PER | US-PFIZER INC-2014314101 | PFIZER | 82.00 | YR | F | Y | 58.00000 | KG | 20141117 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105875001 | 10587500 | 1 | PS | PRISTIQ EXTENDED RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 50 MG, UNK | D | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | |||||||
| 105875001 | 10587500 | 2 | SS | PRISTIQ EXTENDED RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 100 MG, UNK | D | 21992 | 100 | MG | PROLONGED-RELEASE TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105875001 | 10587500 | Depressed mood | |
| 105875001 | 10587500 | Emotional disorder | |
| 105875001 | 10587500 | Feeling abnormal | |
| 105875001 | 10587500 | Panic disorder | |
| 105875001 | 10587500 | Thinking abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |