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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98182803 | 9818280 | 3 | F | 20160902 | 20140115 | 20160908 | EXP | US-PFIZER INC-2010170303 | PFIZER | 0.00 | F | Y | 0.00000 | 20160908 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 98182803 | 9818280 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | UNK | 21992 | PROLONGED-RELEASE TABLET | ||||||||||
| 98182803 | 9818280 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 40 MG, UNK | 21992 | 40 | MG | PROLONGED-RELEASE TABLET | ||||||||
| 98182803 | 9818280 | 3 | SS | CELEBREX | CELECOXIB | 1 | UNK | U | 20998 | CAPSULE, HARD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 98182803 | 9818280 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 98182803 | 9818280 | Back pain | |
| 98182803 | 9818280 | Crying | |
| 98182803 | 9818280 | Dizziness | |
| 98182803 | 9818280 | Drug intolerance | |
| 98182803 | 9818280 | Drug withdrawal syndrome | |
| 98182803 | 9818280 | Emotional disorder | |
| 98182803 | 9818280 | Kidney infection | |
| 98182803 | 9818280 | Psychomotor hyperactivity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |