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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122046388 | 12204638 | 8 | F | 20160809 | 20160323 | 20160819 | PER | PHEH2016US006772 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122046388 | 12204638 | 1 | PS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Oral | 200 MG, BID | F0001, F0002 | 207620 | 200 | MG | TABLET | BID | |||||
| 122046388 | 12204638 | 2 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Oral | 200 MG, QOD (EVERY OTHER DAY) | 207620 | 200 | MG | TABLET | |||||||
| 122046388 | 12204638 | 3 | SS | CARVEDILOL. | CARVEDILOL | 1 | Oral | 12.5 MG, BID | U | 0 | 12.5 | MG | BID | ||||||
| 122046388 | 12204638 | 4 | C | LASIX | FUROSEMIDE | 1 | Oral | 20 MG, QD | U | 0 | 20 | MG | QD | ||||||
| 122046388 | 12204638 | 5 | C | ASPIRIN//ACETYLSALICYLIC ACID | ASPIRIN | 1 | Oral | 81 MG, QD | U | 0 | 81 | MG | QD | ||||||
| 122046388 | 12204638 | 6 | C | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Oral | 100 MG, QD | U | 0 | 100 | MG | QD | ||||||
| 122046388 | 12204638 | 7 | C | GLIMEPIRIDE. | GLIMEPIRIDE | 1 | Oral | 1 MG, BID | U | 0 | 1 | MG | BID | ||||||
| 122046388 | 12204638 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 20 MG, QD | U | 0 | 20 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122046388 | 12204638 | 1 | Cardiac failure |
| 122046388 | 12204638 | 3 | Product used for unknown indication |
| 122046388 | 12204638 | 4 | Cardiac failure congestive |
| 122046388 | 12204638 | 5 | Product used for unknown indication |
| 122046388 | 12204638 | 6 | Diabetes mellitus |
| 122046388 | 12204638 | 7 | Product used for unknown indication |
| 122046388 | 12204638 | 8 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122046388 | 12204638 | Abdominal pain upper | |
| 122046388 | 12204638 | Balance disorder | |
| 122046388 | 12204638 | Blood potassium increased | |
| 122046388 | 12204638 | Contusion | |
| 122046388 | 12204638 | Diarrhoea | |
| 122046388 | 12204638 | Fall | |
| 122046388 | 12204638 | Nausea | |
| 122046388 | 12204638 | Rhinorrhoea | |
| 122046388 | 12204638 | Rib fracture |
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 |
|---|---|---|---|---|---|---|
| 122046388 | 12204638 | 1 | 20160119 | 0 |