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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127375971 | 12737597 | 1 | I | 20131212 | 20160906 | 20160913 | 20160913 | EXP | GB-MHRA-ADR 23625380 | GB-PFIZER INC-2016421725 | PFIZER | 50.00 | YR | F | Y | 85.00000 | KG | 20160913 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127375971 | 12737597 | 1 | PS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 225 MG, 1X/DAY | N | 20699 | 225 | MG | QD | ||||||
| 127375971 | 12737597 | 2 | SS | VENLAFAXINE HCL | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 37.5 MG, 1X/DAY | N | 20699 | 37.5 | MG | QD | ||||||
| 127375971 | 12737597 | 3 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
| 127375971 | 12737597 | 4 | C | BUPROPION. | BUPROPION | 1 | 150 MG, 1X/DAY | 0 | 150 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127375971 | 12737597 | 1 | Major depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127375971 | 12737597 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127375971 | 12737597 | Abdominal discomfort | |
| 127375971 | 12737597 | Abdominal distension | |
| 127375971 | 12737597 | Abdominal pain | |
| 127375971 | 12737597 | Blood triglycerides increased | |
| 127375971 | 12737597 | Faeces discoloured | |
| 127375971 | 12737597 | Gastrointestinal motility disorder | |
| 127375971 | 12737597 | Nausea | |
| 127375971 | 12737597 | 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 |
|---|---|---|---|---|---|---|
| 127375971 | 12737597 | 1 | 2013 | 0 |