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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125456871 | 12545687 | 1 | I | 20160705 | 20160711 | 20160711 | EXP | AU-PFIZER INC-2016332405 | PFIZER | 0.00 | M | Y | 0.00000 | 20160711 | CN | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125456871 | 12545687 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 100 MG, EVERY SECOND DAY | 21992 | 100 | MG | PROLONGED-RELEASE TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125456871 | 12545687 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125456871 | 12545687 | Anal incontinence | |
| 125456871 | 12545687 | Dependence | |
| 125456871 | 12545687 | Disorientation | |
| 125456871 | 12545687 | Dizziness | |
| 125456871 | 12545687 | Fatigue | |
| 125456871 | 12545687 | Feeling of body temperature change | |
| 125456871 | 12545687 | Headache | |
| 125456871 | 12545687 | Hyperhidrosis | |
| 125456871 | 12545687 | Insomnia | |
| 125456871 | 12545687 | Mood swings | |
| 125456871 | 12545687 | Pain | |
| 125456871 | 12545687 | Vomiting | |
| 125456871 | 12545687 | Withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |