Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6808856 | 7447775 | I | 6808856-X | 20090901 | 20090920 | 20100630 | PER | US-PFIZER INC-2009273096 | PFIZERINC | YR | M | Y | 20100629 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6808856 | 1014001444 | PS | TIKOSYN | 1 | UNK | 020931 | |||||
| 6808856 | 1014001445 | I | BENADRYL | 1 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6808856 | 1014001445 | INSOMNIA |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6808856 | DRUG INTERACTION |
| 6808856 | INSOMNIA |
| 6808856 | MALAISE |
| 6808856 | NAUSEA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6808856 | 1014001444 | 20090901 | |||
| 6808856 | 1014001445 | 20090919 |