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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127389283 | 12738928 | 3 | F | 201607 | 20160914 | 20160912 | 20160919 | PER | US-PFIZER INC-2016426201 | PFIZER | 69.00 | YR | M | Y | 75.00000 | KG | 20160919 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127389283 | 12738928 | 1 | PS | VIAGRA | SILDENAFIL CITRATE | 1 | 50 MG, SINGLE, (HALF PILL OF THE 100 MG PILL, ONCE) | Y | 8575401S | 20895 | 50 | MG | FILM-COATED TABLET | ||||||
127389283 | 12738928 | 2 | SS | VIAGRA | SILDENAFIL CITRATE | 1 | 100 MG, UNK (TOOK 1/2 THE DOSAGE) | Y | 20895 | 100 | MG | FILM-COATED TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127389283 | 12738928 | 1 | Blood testosterone decreased |
127389283 | 12738928 | 2 | Erectile dysfunction |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127389283 | 12738928 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127389283 | 12738928 | Blood pressure increased | |
127389283 | 12738928 | Dyspnoea | |
127389283 | 12738928 | Erection increased | |
127389283 | 12738928 | Headache | |
127389283 | 12738928 | Nasal congestion | |
127389283 | 12738928 | Palpitations | |
127389283 | 12738928 | Tachypnoea |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |