FDA Adverse Event
Summary report: N
PROAIR (HFA)
MDR report key: 875515
·
Received July 2, 2007
Report
- Report Number
- MW5002907
- Date Received
- July 2, 2007
- Report Date
- July 2, 2007
- Manufacturer
- UNK
- Product Code
- CCQ
- Report Source
- Voluntary report
- Reporter Location
- FL, US
Narratives
Description of Event or Problem · 1
REPORTER SAYS THAT PRODUCT WAS PRESCRIBED TO HIM AS A REPLACEMENT FOR HIS OWN INHALER. HE HAS COPD. WHENEVER HE USES THE PRODUCT HIS CHEST TIGHTENS, INSTEAD OF IT PROVIDING HIM WITH "RELIEF". HIS OLD INHALER WAS MADE BY ARMSTRONG (ALBUTEROL INHALER). HE WAS TOLD BY THE PHARMACIST THAT THE OLD INHALER WAS DISCONTINUED, BECAUSE OF ITS INTERFERING WITH "THE ATMOSPHERE". HE'S BEEN TOLD THAT OTHERS ARE COMPLAINING ABOUT THE NEW PRODUCT NOT WORKING. HE IS GOING TO CONTACT HIS DOCTOR CONCERNING THE PROBLEM. HE SAYS THE PROAIR INHALER IS "KILLING" HIM!
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PROAIR (HFA) | INHALER | CCQ | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR |