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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125615781 | 12561578 | 1 | I | 201507 | 20160714 | 20160715 | 20160715 | EXP | NO-009507513-1607NOR006753 | MERCK | 25.00 | YR | F | Y | 0.00000 | 20160715 | LW | NO | NO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125615781 | 12561578 | 1 | PS | SINGULAIR | MONTELUKAST SODIUM | 1 | Oral | UNK | 20830 | CHEWABLE TABLET | |||||||||
| 125615781 | 12561578 | 2 | SS | SINGULAIR | MONTELUKAST SODIUM | 1 | 20830 | CHEWABLE TABLET | |||||||||||
| 125615781 | 12561578 | 3 | C | CETIRIZINE HYDROCHLORIDE. | CETIRIZINE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 4 | C | SOMAC | PANTOPRAZOLE SODIUM | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 5 | C | PREDNISOLONE. | PREDNISOLONE | 1 | UNK | U | 0 | TABLET | |||||||||
| 125615781 | 12561578 | 6 | C | ALBYL-E | ASPIRINMAGNESIUM OXIDE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 7 | C | MICROGYNON | ETHINYL ESTRADIOLLEVONORGESTREL ACETATE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 8 | C | ATROVENT | IPRATROPIUM BROMIDE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 9 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 10 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK | U | 0 | ||||||||||
| 125615781 | 12561578 | 11 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125615781 | 12561578 | 1 | Asthma |
| 125615781 | 12561578 | 2 | Hypersensitivity |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125615781 | 12561578 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125615781 | 12561578 | Adverse event | |
| 125615781 | 12561578 | Asthenia | |
| 125615781 | 12561578 | Asthma | |
| 125615781 | 12561578 | Hypersensitivity | |
| 125615781 | 12561578 | Infection | |
| 125615781 | 12561578 | Neurological symptom | |
| 125615781 | 12561578 | Rash |
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 |
|---|---|---|---|---|---|---|
| 125615781 | 12561578 | 1 | 20110101 | 20160512 | 0 |