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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125377772 | 12537777 | 2 | F | 2016 | 20160706 | 20160707 | 20160720 | PER | US-PFIZER INC-2016333862 | PFIZER | 36.00 | YR | F | Y | 54.00000 | KG | 20160720 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125377772 | 12537777 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 200 MG, 2X/DAY | 21992 | 200 | MG | PROLONGED-RELEASE TABLET | BID | |||||||
| 125377772 | 12537777 | 2 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 21992 | PROLONGED-RELEASE TABLET | |||||||||||
| 125377772 | 12537777 | 3 | SS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 21992 | PROLONGED-RELEASE TABLET | |||||||||||
| 125377772 | 12537777 | 4 | C | RINGER-LACTATE | 2 | Intravenous (not otherwise specified) | UNK, THREE TIMES A WEEK | 0 | |||||||||||
| 125377772 | 12537777 | 5 | C | RINGER-LACTATE | 2 | 0 | |||||||||||||
| 125377772 | 12537777 | 6 | C | SALINE /00075401/ | SODIUM CHLORIDE | 1 | Intravenous (not otherwise specified) | UNK, THREE TIMES A WEEK | 0 | ||||||||||
| 125377772 | 12537777 | 7 | C | SALINE /00075401/ | SODIUM CHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125377772 | 12537777 | 1 | Impaired gastric emptying |
| 125377772 | 12537777 | 2 | Pain |
| 125377772 | 12537777 | 3 | Nausea |
| 125377772 | 12537777 | 4 | Dehydration |
| 125377772 | 12537777 | 5 | Malnutrition |
| 125377772 | 12537777 | 6 | Dehydration |
| 125377772 | 12537777 | 7 | Malnutrition |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125377772 | 12537777 | Abnormal dreams | |
| 125377772 | 12537777 | Condition aggravated | |
| 125377772 | 12537777 | Eye disorder | |
| 125377772 | 12537777 | Headache | |
| 125377772 | 12537777 | Hypotension | |
| 125377772 | 12537777 | Migraine | |
| 125377772 | 12537777 | Photopsia | |
| 125377772 | 12537777 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 125377772 | 12537777 | 1 | 201606 | 0 |