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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90996828 | 9099682 | 8 | F | 2010 | 20160830 | 20130214 | 20160907 | EXP | PHHY2012MX085175 | SANDOZ | 0.00 | F | Y | 77.00000 | KG | 20160907 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90996828 | 9099682 | 1 | SS | DIOVAN | VALSARTAN | 1 | Oral | 1 DF (80 MG), QD (IN THE MORNING, 6 OR 7) | 0 | 1 | DF | TABLET | QD | ||||||
| 90996828 | 9099682 | 2 | SS | DIOVAN | VALSARTAN | 1 | Oral | 0.5 DF (160 MG), QD | 0 | .5 | DF | TABLET | QD | ||||||
| 90996828 | 9099682 | 3 | SS | DIOVAN | VALSARTAN | 1 | Oral | 1 DF (80 MG), QD (IN THE MORNING, 6 OR 7) | 0 | 1 | DF | TABLET | QD | ||||||
| 90996828 | 9099682 | 4 | SS | CO-DIOVAN | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Unknown | 1 DF (VALSARTAN 320 MG, HYDROCHLOROTHIAZIDE 12.5 MG), QD | 0 | 1 | DF | QD | |||||||
| 90996828 | 9099682 | 5 | SS | CO-DIOVAN | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Unknown | 2 DF (VALSARTAN 160 MG, HYDROCHLOROTHIAZIDE 12.5 MG), UNK | 0 | 2 | DF | ||||||||
| 90996828 | 9099682 | 6 | PS | LOSARTAN. | LOSARTAN | 1 | Unknown | U | 77424 | ||||||||||
| 90996828 | 9099682 | 7 | C | CALCIUM | CALCIUM | 1 | Unknown | U | 0 | ||||||||||
| 90996828 | 9099682 | 8 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Oral | 1 DF, QD | 0 | 1 | DF | TABLET | QD | ||||||
| 90996828 | 9099682 | 9 | C | GLUCOSAMINE | GLUCOSAMINE | 1 | Unknown | U | 0 | ||||||||||
| 90996828 | 9099682 | 10 | C | METOPROLOL. | METOPROLOL | 1 | Oral | 1 DF, UNK | 0 | 1 | DF | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 90996828 | 9099682 | 1 | Hypertension |
| 90996828 | 9099682 | 4 | Hypertension |
| 90996828 | 9099682 | 6 | Product used for unknown indication |
| 90996828 | 9099682 | 7 | Product used for unknown indication |
| 90996828 | 9099682 | 8 | Hypothyroidism |
| 90996828 | 9099682 | 9 | Product used for unknown indication |
| 90996828 | 9099682 | 10 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 90996828 | 9099682 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 90996828 | 9099682 | Arthropathy | |
| 90996828 | 9099682 | Blood pressure inadequately controlled | |
| 90996828 | 9099682 | Cardiomegaly | |
| 90996828 | 9099682 | Concomitant disease aggravated | |
| 90996828 | 9099682 | Drug prescribing error | |
| 90996828 | 9099682 | Fatigue | |
| 90996828 | 9099682 | Incorrect dose administered | |
| 90996828 | 9099682 | Influenza | |
| 90996828 | 9099682 | Nasopharyngitis | |
| 90996828 | 9099682 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 90996828 | 9099682 | 1 | 2005 | 0 | ||
| 90996828 | 9099682 | 2 | 200606 | 200607 | 0 | |
| 90996828 | 9099682 | 10 | 201602 | 0 |