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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125694411 | 12569441 | 1 | I | 20150330 | 20160719 | 20160719 | PER | US-PFIZER INC-2015116064 | PFIZER | 61.00 | YR | F | Y | 81.63000 | KG | 20160719 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125694411 | 12569441 | 1 | PS | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Oral | 50 MG, 1X/DAY | U | 21992 | 50 | MG | PROLONGED-RELEASE TABLET | QD | |||||
125694411 | 12569441 | 2 | C | GABAPENTIN. | GABAPENTIN | 1 | UNK | 0 | |||||||||||
125694411 | 12569441 | 3 | C | XANAX | ALPRAZOLAM | 1 | UNK | 0 | |||||||||||
125694411 | 12569441 | 4 | C | ACICLOVIR | ACYCLOVIR | 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 |
---|---|---|---|
125694411 | 12569441 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |