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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6808857 | 7447776 | I | 6808857-1 | 20090925 | 20100630 | PER | US-PFIZER INC-2009275670 | PFIZERINC | YR | F | Y | 20100629 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6808857 | 1014001446 | PS | VIAGRA | 1 | UNK | 020895 | |||||
6808857 | 1014001447 | SS | VIAGRA | 1 | 020895 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6808857 | 1014001446 | SCLERODERMA |
6808857 | 1014001447 | CARDIOVASCULAR DISORDER |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6808857 | CYANOPSIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |