Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6811820 | 7457647 | I | 6811820-8 | 20100310 | 20100609 | 20100628 | EXP | 7007322 | DE-MERCK KGAA | 90 | YR | F | N | 20100614 | FRANCE |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6811820 | 1014012792 | PS | BISOPROLOL FUMARATE | 1 | ORAL | ORAL | D | D | 21292 | ||
6811820 | 1014054820 | SS | LEVOTHYROXINE SODIUM | 1 | ORAL | 1 DF (1 DF, 1 IN 1 D); ORAL | |||||
6811820 | 1014054823 | SS | ACTOS | 1 | ORAL | 1 DF (1 DF, 1 IN 1 D); ORAL | |||||
6811820 | 1014054826 | SS | COVERSYL (PERINDOPRIL) (TABLET) (PERINDORPIL) | 2 | ORAL | ORAL | |||||
6811820 | 1014054835 | SS | AMARYL | 1 | ORAL | ORAL | |||||
6811820 | 1014054837 | SS | LASIX | 1 | ORAL | 2 DF (2 DF, 1 D); ORAL | |||||
6811820 | 1014054838 | SS | ALDACTONE | 1 | ORAL | 1 DG (1 DF, 1 IN 1 D); ORAL | |||||
6811820 | 1014054842 | SS | POTASSIUM CHLORIDE | 1 | ORAL | 1 DF (1 DF, 1 IN 1 D); ORAL | |||||
6811820 | 1014054844 | SS | PREVISCAN (FLUINDIONE) (TABLET) (FLUINDIONE) | 2 | ORAL | 15 MG (15 MG, 1 IN 1 D); ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6811820 | 1014012792 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054820 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054823 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054826 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054835 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054837 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054838 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054842 | DRUG USE FOR UNKNOWN INDICATION |
6811820 | 1014054844 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6811820 | HO |
Reactions reported
Event ID | PT |
---|---|
6811820 | AORTIC VALVE STENOSIS |
6811820 | BRADYCARDIA |
6811820 | CARDIAC FAILURE |
6811820 | CARDIOMEGALY |
6811820 | DYSPNOEA |
6811820 | OEDEMA PERIPHERAL |
6811820 | OLIGURIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6811820 | FGN |
6811820 | HP |
6811820 | OTH |
Therapies reported
no results found |