Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7299472 | 7778801 | F | 7299472-7 | 20101001 | 20110215 | 20110217 | EXP | D0070096A | GLAXOSMITHKLINE | 45 | YR | F | Y | 73 | KG | 20110217 | CN | GERMANY |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7299472 | 1015808085 | C | SINGULAIR | 1 | ORAL | ||||||
| 7299472 | 1015808086 | C | XOLAIR | 1 | SUBCUTANEOUS | ||||||
| 7299472 | 1015808084 | PS | ATMADISC FORTE | 2 | RESPIRATORY (INHALATION) | 2PUFF TWICE PER DAY | 021077 | ||||
| 7299472 | 1015808087 | C | BEROTEC | 1 | RESPIRATORY (INHALATION) |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7299472 | 1015808085 | ASTHMA |
| 7299472 | 1015808086 | ASTHMA |
| 7299472 | 1015808084 | ASTHMA |
| 7299472 | 1015808087 | ASTHMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7299472 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7299472 | LARYNGITIS |
| 7299472 | EPIGLOTTITIS |
| 7299472 | COUGH |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7299472 | 1015808085 | 20090901 | |||
| 7299472 | 1015808084 | 20090901 | 20110131 | 16 | MON |
| 7299472 | 1015808087 | 20070101 |