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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126710711 | 12671071 | 1 | I | 20160504 | 20160810 | 20160822 | 20160822 | EXP | CN-PFIZER INC-2016387917 | PFIZER | 63.00 | YR | M | Y | 63.00000 | KG | 20160822 | OT | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126710711 | 12671071 | 1 | PS | GLUCOTROL XL | GLIPIZIDE | 1 | Oral | 5 MG, 1X/DAY | 5 | MG | Y | J85543 | 20329 | 5 | MG | GASTRO-RESISTANT TABLET | QD | ||
126710711 | 12671071 | 2 | SS | ANDUOMEI | GLIMEPIRIDE | 1 | Oral | 2 MG, 1X/DAY | 30 | MG | Y | 20160201 | 0 | 2 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126710711 | 12671071 | 1 | Diabetes mellitus |
126710711 | 12671071 | 2 | Diabetes mellitus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126710711 | 12671071 | HO |
126710711 | 12671071 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126710711 | 12671071 | Anaemia | |
126710711 | 12671071 | Hypoglycaemic coma | |
126710711 | 12671071 | Hypokalaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
126710711 | 12671071 | 1 | 20160503 | 20160503 | 0 | |
126710711 | 12671071 | 2 | 20160419 | 20160503 | 0 |