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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127226801 | 12722680 | 1 | I | 20160711 | 20160901 | 20160907 | 20160907 | PER | US-PFIZER INC-2016416126 | PFIZER | 54.00 | YR | M | Y | 73.00000 | KG | 20160907 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127226801 | 12722680 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | 100 MG, DAILY (EVERY MORNING) | Y | 21992 | 100 | MG | PROLONGED-RELEASE TABLET | |||||||
| 127226801 | 12722680 | 2 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 127226801 | 12722680 | 3 | C | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127226801 | 12722680 | 1 | Depression |
| 127226801 | 12722680 | 2 | Abdominal discomfort |
| 127226801 | 12722680 | 3 | Abdominal discomfort |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127226801 | 12722680 | Disturbance in attention | |
| 127226801 | 12722680 | Dyspepsia | |
| 127226801 | 12722680 | Hypersensitivity | |
| 127226801 | 12722680 | Intentional product misuse | |
| 127226801 | 12722680 | Nausea | |
| 127226801 | 12722680 | Nervousness | |
| 127226801 | 12722680 | Night sweats | |
| 127226801 | 12722680 | Pruritus | |
| 127226801 | 12722680 | Urticaria | |
| 127226801 | 12722680 | Withdrawal syndrome |
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 |
|---|---|---|---|---|---|---|
| 127226801 | 12722680 | 1 | 2007 | 201608 | 0 |