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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127478341 | 12747834 | 1 | I | 201608 | 20160907 | 20160915 | 20160915 | PER | US-ELI_LILLY_AND_COMPANY-US201609002238 | ELI LILLY AND CO | 74.00 | YR | M | Y | 0.00000 | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127478341 | 12747834 | 1 | PS | EFFIENT | PRASUGREL HYDROCHLORIDE | 1 | Unknown | 10 MG, EACH MORNING | Y | U | C553964A | 22307 | 10 | MG | TABLET | QD | |||
| 127478341 | 12747834 | 2 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 3 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 4 | C | ATORVASTATIN | ATORVASTATIN | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 5 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 6 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 7 | C | FLUTICASONE | FLUTICASONEFLUTICASONE PROPIONATE | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 8 | C | TUDORZA GENUAIR | ACLIDINIUM BROMIDE | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 9 | C | MUCINEX DM | DEXTROMETHORPHAN HYDROBROMIDEGUAIFENESIN | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 10 | C | MUCINEX | GUAIFENESIN | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 11 | C | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 127478341 | 12747834 | 12 | C | CENTRUM SILVER /02363801/ | MINERALSVITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127478341 | 12747834 | 1 | Stent placement |
| 127478341 | 12747834 | 2 | Product used for unknown indication |
| 127478341 | 12747834 | 3 | Product used for unknown indication |
| 127478341 | 12747834 | 4 | Product used for unknown indication |
| 127478341 | 12747834 | 5 | Product used for unknown indication |
| 127478341 | 12747834 | 6 | Product used for unknown indication |
| 127478341 | 12747834 | 7 | Product used for unknown indication |
| 127478341 | 12747834 | 8 | Product used for unknown indication |
| 127478341 | 12747834 | 9 | Product used for unknown indication |
| 127478341 | 12747834 | 10 | Product used for unknown indication |
| 127478341 | 12747834 | 11 | Hypersensitivity |
| 127478341 | 12747834 | 12 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127478341 | 12747834 | Chest discomfort | |
| 127478341 | 12747834 | Chest pain | |
| 127478341 | 12747834 | Drug dose omission | |
| 127478341 | 12747834 | Dyspnoea |
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 |
|---|---|---|---|---|---|---|
| 127478341 | 12747834 | 1 | 201606 | 20160831 | 0 |