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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127391641 | 12739164 | 1 | I | 20160525 | 20160905 | 20160912 | 20160912 | EXP | JP-PFIZER INC-2016419171 | PFIZER | 73.00 | YR | F | Y | 0.00000 | 20160912 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127391641 | 12739164 | 1 | PS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 225 MG, DAILY | 20699 | 225 | MG | PROLONGED-RELEASE CAPSULE | |||||||
| 127391641 | 12739164 | 2 | SS | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 225 MG, DAILY | 20699 | 225 | MG | PROLONGED-RELEASE CAPSULE | |||||||
| 127391641 | 12739164 | 3 | SS | ZYPREXA | OLANZAPINE | 1 | Oral | 1.25 MG, DAILY | 0 | 1.25 | MG | ||||||||
| 127391641 | 12739164 | 4 | SS | ZYPREXA | OLANZAPINE | 1 | Oral | 2.5 MG, DAILY | 0 | 2.5 | MG | ||||||||
| 127391641 | 12739164 | 5 | C | VASOLAN | VERAPAMIL HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 127391641 | 12739164 | 6 | C | LOSARTAN. | LOSARTAN | 1 | UNK | 0 | |||||||||||
| 127391641 | 12739164 | 7 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | UNK | 0 | |||||||||||
| 127391641 | 12739164 | 8 | C | ATORVASTATIN | ATORVASTATIN | 1 | UNK | 0 | |||||||||||
| 127391641 | 12739164 | 9 | C | MAGMITT | MAGNESIUM OXIDE | 1 | UNK | 0 | |||||||||||
| 127391641 | 12739164 | 10 | C | GASTER | FAMOTIDINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127391641 | 12739164 | 1 | Depression |
| 127391641 | 12739164 | 3 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127391641 | 12739164 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127391641 | 12739164 | Decreased appetite | |
| 127391641 | 12739164 | Disease recurrence | |
| 127391641 | 12739164 | Dizziness | |
| 127391641 | 12739164 | Insomnia | |
| 127391641 | 12739164 | Intestinal obstruction |
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 |
|---|---|---|---|---|---|---|
| 127391641 | 12739164 | 1 | 20160531 | 0 | ||
| 127391641 | 12739164 | 2 | 20160606 | 0 | ||
| 127391641 | 12739164 | 3 | 20160610 | 0 | ||
| 127391641 | 12739164 | 4 | 20160611 | 0 |