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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127201612 | 12720161 | 2 | F | 201608 | 20160913 | 20160907 | 20160914 | PER | US-PFIZER INC-2016416749 | PFIZER | 64.00 | YR | F | Y | 0.00000 | 20160914 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127201612 | 12720161 | 1 | PS | SILDENAFIL CITRATE. | SILDENAFIL CITRATE | 1 | Unknown | 20 MG, 3X/DAY | Y | 21845 | 20 | MG | FILM-COATED TABLET | TID | |||||
127201612 | 12720161 | 2 | SS | SILDENAFIL CITRATE. | SILDENAFIL CITRATE | 1 | Unknown | 20 MG, 2X/DAY | Y | 21845 | 20 | MG | FILM-COATED TABLET | BID | |||||
127201612 | 12720161 | 3 | SS | REMODULIN | TREPROSTINIL | 1 | Intravenous drip | 0.025 UG/KG, UNK (1MG/ML) | 0 | .025 | UG/KG | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127201612 | 12720161 | 3 | Pulmonary arterial hypertension |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127201612 | 12720161 | Clitoral engorgement | |
127201612 | 12720161 | Vulvovaginal swelling |
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 |
---|---|---|---|---|---|---|
127201612 | 12720161 | 3 | 20120716 | 0 |