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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126477661 | 12647766 | 1 | I | 20160722 | 20160808 | 20160812 | 20160812 | EXP | IT-PFIZER INC-2016380708 | PFIZER | 37.00 | YR | M | Y | 0.00000 | 20160812 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126477661 | 12647766 | 1 | PS | XANAX | ALPRAZOLAM | 1 | Oral | UNK | 18276 | ORAL DROPS, SOLUTION | |||||||||
| 126477661 | 12647766 | 2 | SS | SPORANOX | ITRACONAZOLE | 1 | Oral | UNK | 0 | ||||||||||
| 126477661 | 12647766 | 3 | SS | DOMPERIDONE | DOMPERIDONE | 1 | Oral | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126477661 | 12647766 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126477661 | 12647766 | Drug abuse | |
| 126477661 | 12647766 | Intentional self-injury | |
| 126477661 | 12647766 | Sopor |
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 |
|---|---|---|---|---|---|---|
| 126477661 | 12647766 | 1 | 20160722 | 20160722 | 0 | |
| 126477661 | 12647766 | 2 | 20160722 | 20160722 | 0 | |
| 126477661 | 12647766 | 3 | 20160722 | 20160722 | 0 |