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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126165943 | 12616594 | 3 | F | 20160513 | 20160720 | 20160802 | 20160818 | EXP | IT-MINISAL02-368046 | IT-TEVA-680195ACC | TEVA | 71.06 | YR | F | Y | 0.00000 | 20160818 | OT | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126165943 | 12616594 | 1 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 0 | 1 | DF | ||||||
126165943 | 12616594 | 2 | PS | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 76999 | 1 | DF | ||||||
126165943 | 12616594 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 0 | 1 | DF | ||||||
126165943 | 12616594 | 4 | SS | TOLEP - NOVARTIS FARMA S.P.A. | OXCARBAZEPINE | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 0 | 1 | DF | ||||||
126165943 | 12616594 | 5 | SS | NORVASC | AMLODIPINE BESYLATE | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 0 | 1 | DF | ||||||
126165943 | 12616594 | 6 | SS | TAREG - NOVARTIS EUROPHARM LTD | VALSARTAN | 1 | Oral | 1 DOSAGE FORMS DAILY; | U | U | 0 | 1 | DF |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126165943 | 12616594 | 1 | Diabetes mellitus |
126165943 | 12616594 | 2 | Thrombosis prophylaxis |
126165943 | 12616594 | 3 | Hypertension |
126165943 | 12616594 | 4 | Epilepsy |
126165943 | 12616594 | 5 | Hypertension |
126165943 | 12616594 | 6 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126165943 | 12616594 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126165943 | 12616594 | Dyspnoea | |
126165943 | 12616594 | Palpitations |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |