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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112184576 | 11218457 | 6 | F | 20160715 | 20150625 | 20160721 | EXP | US-PFIZER INC-2015206800 | PFIZER | 68.00 | YR | F | Y | 0.00000 | 20160721 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
112184576 | 11218457 | 1 | PS | REVATIO | SILDENAFIL CITRATE | 1 | 20 MG, 3X/DAY | 21845 | 20 | MG | FILM-COATED TABLET | TID | |||||||
112184576 | 11218457 | 2 | SS | REVATIO | SILDENAFIL CITRATE | 1 | ^200^ MG, 4 TABLETS THREE TIMES A DAY | 21845 | FILM-COATED TABLET | TID |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
112184576 | 11218457 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
112184576 | 11218457 | Alopecia | |
112184576 | 11218457 | Contusion | |
112184576 | 11218457 | Cough | |
112184576 | 11218457 | Dyspepsia | |
112184576 | 11218457 | Hair growth abnormal | |
112184576 | 11218457 | Intentional product use issue | |
112184576 | 11218457 | Skin atrophy |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |