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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125867791 | 12586779 | 1 | I | 20160713 | 20160725 | 20160725 | PER | US-PFIZER INC-2016345544 | PFIZER | 68.00 | YR | F | Y | 79.37000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125867791 | 12586779 | 1 | PS | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | UNK | 19839 | |||||||||||
| 125867791 | 12586779 | 2 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | 500 MG, 2X/DAY | 0 | 500 | MG | BID | ||||||||
| 125867791 | 12586779 | 3 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | 500 MG, 1X/DAY | 0 | 500 | MG | QD | ||||||||
| 125867791 | 12586779 | 4 | SS | NAMENDA | MEMANTINE HYDROCHLORIDE | 1 | 2X/DAY | 0 | BID | ||||||||||
| 125867791 | 12586779 | 5 | SS | NAMENDA | MEMANTINE HYDROCHLORIDE | 1 | 1X/DAY | 0 | QD | ||||||||||
| 125867791 | 12586779 | 6 | SS | SEROQUEL | QUETIAPINE FUMARATE | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125867791 | 12586779 | Feeling abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |