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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125901551 | 12590155 | 1 | I | 20160721 | 20160725 | 20160725 | EXP | GB-GLAXOSMITHKLINE-GB2016GSK106677 | GLAXOSMITHKLINE | 0.00 | M | Y | 0.00000 | 20160725 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125901551 | 12590155 | 1 | PS | Zeffix | LAMIVUDINE | 1 | 100 MG, UNK | U | 21003 | 100 | MG | ||||||||
125901551 | 12590155 | 2 | SS | TENOFOVIR DISOPROXIL FUMARATE. | TENOFOVIR DISOPROXIL FUMARATE | 1 | 245 MG, UNK | U | 0 | 245 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125901551 | 12590155 | 1 | Hepatitis |
125901551 | 12590155 | 2 | Hepatitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125901551 | 12590155 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125901551 | 12590155 | Infection | |
125901551 | 12590155 | Malaise |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |