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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127272022 | 12727202 | 2 | F | 20160906 | 20160909 | 20160909 | PER | PHEH2016US022541 | SANDOZ | 0.00 | M | Y | 0.00000 | 20160909 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127272022 | 12727202 | 1 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Unknown | 100 MG (49/51 MG), BID | 0 | 100 | MG | BID | |||||||
| 127272022 | 12727202 | 2 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Unknown | 50 MG (24/26 MG), QD | 0 | 50 | MG | QD | |||||||
| 127272022 | 12727202 | 3 | PS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | UNK | 86809 | ||||||||||
| 127272022 | 12727202 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 6 | C | LATANOPROST. | LATANOPROST | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 7 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 8 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 9 | C | FISH OIL | FISH OIL | 1 | Unknown | UNK | U | 0 | |||||||||
| 127272022 | 12727202 | 10 | C | COQ10 | UBIDECARENONE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127272022 | 12727202 | 1 | Product used for unknown indication |
| 127272022 | 12727202 | 3 | Product used for unknown indication |
| 127272022 | 12727202 | 4 | Product used for unknown indication |
| 127272022 | 12727202 | 5 | Product used for unknown indication |
| 127272022 | 12727202 | 6 | Product used for unknown indication |
| 127272022 | 12727202 | 7 | Product used for unknown indication |
| 127272022 | 12727202 | 8 | Product used for unknown indication |
| 127272022 | 12727202 | 9 | Product used for unknown indication |
| 127272022 | 12727202 | 10 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127272022 | 12727202 | Back pain | |
| 127272022 | 12727202 | Blood potassium increased | |
| 127272022 | 12727202 | Dizziness | |
| 127272022 | 12727202 | Drug prescribing error |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |