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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125598661 | 12559866 | 1 | I | 20160527 | 20160707 | 20160715 | 20160715 | EXP | IT-PFIZER INC-2016337041 | PFIZER | 23.00 | YR | F | Y | 0.00000 | 20160715 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125598661 | 12559866 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | Oral | 2 DF, TOTAL | U | 20235 | 2 | DF | |||||||
125598661 | 12559866 | 2 | SS | CARBOLITHIUM | LITHIUM CARBONATE | 1 | Oral | 10 DF,TOTAL | U | 0 | 10 | DF | TABLET | ||||||
125598661 | 12559866 | 3 | SS | VALIUM | DIAZEPAM | 1 | Oral | UNK | U | 0 | ORAL DROPS, SOLUTION |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125598661 | 12559866 | HO |
125598661 | 12559866 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125598661 | 12559866 | Drug abuse | |
125598661 | 12559866 | Malaise | |
125598661 | 12559866 | Nausea | |
125598661 | 12559866 | Suicide attempt |
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 |
---|---|---|---|---|---|---|
125598661 | 12559866 | 1 | 20160527 | 20160527 | 0 | |
125598661 | 12559866 | 2 | 20160527 | 20160527 | 0 | |
125598661 | 12559866 | 3 | 20160527 | 20160527 | 0 |