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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122202322 | 12220232 | 2 | F | 20160921 | 20160330 | 20160928 | EXP | PHEH2016US007204 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160928 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122202322 | 12220232 | 1 | PS | DIOVAN HCT | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Unknown | 1 DF, (160 MG VALSARTAN AND 25 MG HYDROCHLOROTHIAZIDE) | U | 20818 | 1 | DF | TABLET | ||||||
122202322 | 12220232 | 2 | SS | VALSARTAN. | VALSARTAN | 1 | Unknown | U | 0 | ||||||||||
122202322 | 12220232 | 3 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | Unknown | 50 MG, UNK | U | 0 | 50 | MG | |||||||
122202322 | 12220232 | 4 | C | TIAZAC | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | 160 MG, UNK | U | 0 | 160 | MG | |||||||
122202322 | 12220232 | 5 | C | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | Unknown | U | 0 | ||||||||||
122202322 | 12220232 | 6 | C | MECLIZINE | MECLIZINE HYDROCHLORIDE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122202322 | 12220232 | 1 | Product used for unknown indication |
122202322 | 12220232 | 2 | Product used for unknown indication |
122202322 | 12220232 | 3 | Product used for unknown indication |
122202322 | 12220232 | 4 | Blood pressure measurement |
122202322 | 12220232 | 5 | Diabetes mellitus |
122202322 | 12220232 | 6 | Vertigo |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122202322 | 12220232 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122202322 | 12220232 | Cough | |
122202322 | 12220232 | Drug prescribing error | |
122202322 | 12220232 | Feeling abnormal | |
122202322 | 12220232 | Renal cancer recurrent |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |