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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123838967 | 12383896 | 7 | F | 20160913 | 20160519 | 20160922 | EXP | PHEH2016US011850 | SANDOZ | 0.00 | M | Y | 0.00000 | 20160922 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123838967 | 12383896 | 1 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Oral | 200 MG, BID | U | F0008 | 0 | 200 | MG | BID | |||||
| 123838967 | 12383896 | 2 | PS | CARVEDILOL. | CARVEDILOL | 1 | Unknown | 6.25 MG, BID | U | 78227 | 6.25 | MG | BID | ||||||
| 123838967 | 12383896 | 3 | C | COREG | CARVEDILOL | 1 | Oral | 12.5 MG, BID | U | 0 | 12.5 | MG | BID | ||||||
| 123838967 | 12383896 | 4 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 81 MG, QD | U | 0 | 81 | MG | QD | ||||||
| 123838967 | 12383896 | 5 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | 300 MG, UNK | U | 0 | 300 | MG | |||||||
| 123838967 | 12383896 | 6 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Oral | 25 MG, QD | U | 0 | 25 | MG | QD | ||||||
| 123838967 | 12383896 | 7 | C | KEFLEX | CEPHALEXIN | 1 | Unknown | 500 MG, UNK | U | 0 | 500 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123838967 | 12383896 | 1 | Cardiac failure |
| 123838967 | 12383896 | 2 | Product used for unknown indication |
| 123838967 | 12383896 | 3 | Product used for unknown indication |
| 123838967 | 12383896 | 4 | Product used for unknown indication |
| 123838967 | 12383896 | 5 | Product used for unknown indication |
| 123838967 | 12383896 | 6 | Product used for unknown indication |
| 123838967 | 12383896 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123838967 | 12383896 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123838967 | 12383896 | Bladder cancer | |
| 123838967 | 12383896 | Dizziness | |
| 123838967 | 12383896 | Drug ineffective | |
| 123838967 | 12383896 | Dyspnoea exertional | |
| 123838967 | 12383896 | Hypotension | |
| 123838967 | 12383896 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |