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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125671351 | 12567135 | 1 | I | 20160324 | 20160718 | 20160718 | PER | US-PFIZER INC-3229033 | PFIZER | 0.00 | M | Y | 0.00000 | 20160718 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125671351 | 12567135 | 1 | PS | DIAZEPAM. | DIAZEPAM | 1 | UNK | U | UNK | 71583 | |||||||||
| 125671351 | 12567135 | 2 | SS | DIAZEPAM. | DIAZEPAM | 1 | U | 71583 | |||||||||||
| 125671351 | 12567135 | 3 | SS | CHANTIX | VARENICLINE TARTRATE | 1 | UNK | U | UNK | 21928 | FILM-COATED TABLET | ||||||||
| 125671351 | 12567135 | 4 | SS | DEPAKOTE | DIVALPROEX SODIUM | 1 | UNK | U | UNK | 0 | |||||||||
| 125671351 | 12567135 | 5 | SS | VALPROIC ACID. | VALPROIC ACID | 1 | UNK | U | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125671351 | 12567135 | 1 | Palpitations |
| 125671351 | 12567135 | 2 | Seizure |
| 125671351 | 12567135 | 3 | Seizure |
| 125671351 | 12567135 | 4 | Seizure |
| 125671351 | 12567135 | 5 | Seizure |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125671351 | 12567135 | Drug ineffective | |
| 125671351 | 12567135 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |