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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6194994 | 6997730 | I | 6194994-4 | 20090501 | 20090512 | 20090519 | EXP | A0783756A | GLAXOSMITHKLINE | 76 | YR | M | Y | 20090519 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6194994 | 1011592778 | PS | ADVAIR HFA | 1 | RESPIRATORY (INHALATION) | R342393 | 021077 | ||||
| 6194994 | 1011592779 | C | DILTIAZEM | 1 | |||||||
| 6194994 | 1011592780 | C | NEXIUM | 1 | |||||||
| 6194994 | 1011592781 | C | POTASSIUM CHLORIDE | 1 | |||||||
| 6194994 | 1011592782 | C | FUROSEMIDE | 1 | |||||||
| 6194994 | 1011592783 | C | SINGULAIR | 1 | |||||||
| 6194994 | 1011592784 | C | COUMADIN | 1 | |||||||
| 6194994 | 1011592785 | C | ENALAPRIL | 2 | |||||||
| 6194994 | 1011592786 | C | XOPENEX | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6194994 | 1011592778 | ASTHMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6194994 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6194994 | DYSPNOEA |
| 6194994 | HYPERTENSION |
| 6194994 | PRODUCT QUALITY ISSUE |
| 6194994 | PULMONARY CONGESTION |
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 |
|---|---|---|---|---|---|
| 6194994 | 1011592778 | 20020101 | 7 | YR |