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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127568862 | 12756886 | 2 | F | 20160910 | 20160923 | 20160917 | 20160926 | PER | US-009507513-1609USA007066 | MERCK | 59.03 | YR | F | Y | 0.00000 | 20160926 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127568862 | 12756886 | 1 | PS | PROVENTIL | ALBUTEROL | 1 | Oral | UNK | 150356 | 20503 | INHALATION POWDER | ||||||||
| 127568862 | 12756886 | 2 | C | HYDREA | HYDROXYUREA | 1 | 0 | ||||||||||||
| 127568862 | 12756886 | 3 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | 0 | ||||||||||||
| 127568862 | 12756886 | 4 | C | LAMICTAL | LAMOTRIGINE | 1 | 0 | ||||||||||||
| 127568862 | 12756886 | 5 | C | TYLENOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 127568862 | 12756886 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127568862 | 12756886 | 1 | Asthma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127568862 | 12756886 | Chest discomfort | |
| 127568862 | 12756886 | Cough |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |