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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126459312 | 12645931 | 2 | F | 20160224 | 20160811 | 20160829 | PER | US-PFIZER INC-2016121854 | PFIZER | 83.00 | YR | M | Y | 70.00000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126459312 | 12645931 | 1 | PS | ERYTHROMYCIN. | ERYTHROMYCIN | 1 | 250 MG, 2X/DAY, THE FIRST DAY | U | 50609 | 250 | MG | BID | |||||||
126459312 | 12645931 | 2 | SS | ERYTHROMYCIN. | ERYTHROMYCIN | 1 | 250 MG, 1X/DAY | U | 50609 | 250 | MG | QD | |||||||
126459312 | 12645931 | 3 | C | VALSARTAN. | VALSARTAN | 1 | Oral | 160 MG, 1X/DAY | 0 | 160 | MG | TABLET | QD | ||||||
126459312 | 12645931 | 4 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | Oral | 10 MG, 1X/DAY | 0 | 10 | MG | TABLET | QD | ||||||
126459312 | 12645931 | 5 | C | TAMSULOSIN HCL | TAMSULOSIN | 1 | Oral | 0.4 MG, 1X/DAY | 0 | .4 | MG | QD | |||||||
126459312 | 12645931 | 6 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | 250 MG, AS NEEDED, IF HIS BLOOD SUGAR IS 180 OR HIGHER | 0 | 250 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126459312 | 12645931 | 1 | Influenza |
126459312 | 12645931 | 3 | Hypertension |
126459312 | 12645931 | 4 | Blood cholesterol increased |
126459312 | 12645931 | 5 | Prostatomegaly |
126459312 | 12645931 | 6 | Diabetes mellitus |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126459312 | 12645931 | Cough | |
126459312 | 12645931 | Diarrhoea | |
126459312 | 12645931 | Product use issue |
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 |
---|---|---|---|---|---|---|
126459312 | 12645931 | 1 | 20160212 | 0 |