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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125880172 | 12588017 | 2 | F | 201605 | 20160829 | 20160725 | 20160906 | EXP | JP-PFIZER INC-2016355720 | PFIZER | 0.00 | F | Y | 0.00000 | 20160906 | MD | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125880172 | 12588017 | 1 | PS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | UNK | Y | 20699 | PROLONGED-RELEASE CAPSULE | ||||||||
| 125880172 | 12588017 | 2 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 150 MG, DAILY | Y | 20699 | 150 | MG | PROLONGED-RELEASE CAPSULE | ||||||
| 125880172 | 12588017 | 3 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 225 MG, DAILY | Y | 20699 | 225 | MG | PROLONGED-RELEASE CAPSULE | ||||||
| 125880172 | 12588017 | 4 | C | LAMICTAL | LAMOTRIGINE | 1 | Oral | 125 MG, DAILY | 0 | 125 | MG | ||||||||
| 125880172 | 12588017 | 5 | C | DEPAKENE | VALPROIC ACID | 1 | Oral | 200 MG, DAILY | 0 | 200 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125880172 | 12588017 | 1 | Depression |
| 125880172 | 12588017 | 4 | Depression |
| 125880172 | 12588017 | 5 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125880172 | 12588017 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125880172 | 12588017 | Abdominal pain upper | |
| 125880172 | 12588017 | Erosive oesophagitis | |
| 125880172 | 12588017 | Gastrooesophageal reflux disease | |
| 125880172 | 12588017 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 125880172 | 12588017 | 1 | 2016 | 2016 | 0 | |
| 125880172 | 12588017 | 2 | 20160502 | 20160606 | 0 | |
| 125880172 | 12588017 | 3 | 20160606 | 20160619 | 0 | |
| 125880172 | 12588017 | 4 | 2013 | 0 | ||
| 125880172 | 12588017 | 5 | 2013 | 0 |