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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126619231 | 12661923 | 1 | I | 20160810 | 20160817 | 20160817 | EXP | MX-ELI_LILLY_AND_COMPANY-MX201608007564 | ELI LILLY AND CO | 54.00 | YR | M | Y | 0.00000 | 20160817 | CN | MX | MX |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126619231 | 12661923 | 1 | PS | CIALIS | TADALAFIL | 1 | Oral | 20 MG, PRN | U | 21368 | 20 | MG | TABLET | ||||||
126619231 | 12661923 | 2 | SS | CIALIS | TADALAFIL | 1 | Oral | 5 MG, QD | U | 21368 | 5 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126619231 | 12661923 | 1 | Erectile dysfunction |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126619231 | 12661923 | Back pain | |
126619231 | 12661923 | Benign prostatic hyperplasia | |
126619231 | 12661923 | Erectile dysfunction | |
126619231 | 12661923 | Headache | |
126619231 | 12661923 | Prostatitis | |
126619231 | 12661923 | Tachycardia | |
126619231 | 12661923 | Vision blurred |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |