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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126833361 | 12683336 | 1 | I | 20160820 | 20160825 | 20160825 | PER | US-PFIZER INC-2016397370 | PFIZER | 45.00 | YR | M | Y | 73.00000 | KG | 20160825 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126833361 | 12683336 | 1 | PS | VIAGRA | SILDENAFIL CITRATE | 1 | Oral | 100 MG, UNK | U | 20895 | 100 | MG | FILM-COATED TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126833361 | 12683336 | 1 | Erectile dysfunction |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126833361 | 12683336 | Abdominal discomfort | |
126833361 | 12683336 | Cyanopsia | |
126833361 | 12683336 | Headache | |
126833361 | 12683336 | Hiccups | |
126833361 | 12683336 | Photopsia |
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 |
---|---|---|---|---|---|---|
126833361 | 12683336 | 1 | 20160819 | 0 |