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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125993672 | 12599367 | 2 | F | 20160912 | 20160727 | 20160914 | EXP | US-PFIZER INC-2016356820 | PFIZER | 77.00 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125993672 | 12599367 | 1 | PS | REVATIO | SILDENAFIL CITRATE | 1 | 20 MG, 3X/DAY | U | A563501 | 21845 | 20 | MG | FILM-COATED TABLET | TID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125993672 | 12599367 | 1 | Pulmonary hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125993672 | 12599367 | HO |
125993672 | 12599367 | DE |
125993672 | 12599367 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125993672 | 12599367 | Atrial fibrillation | |
125993672 | 12599367 | Cardiac failure congestive | |
125993672 | 12599367 | Dementia | |
125993672 | 12599367 | Pneumonia | |
125993672 | 12599367 | Renal failure | |
125993672 | 12599367 | Respiratory failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |