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Fluticasone Propionate; Salmeterol Xinafoate Related Cataract

Official FDA Reports644
Social Media Events3
Active Ingredients
  • Fluticasone Propionate; Salmeterol Xinafoate
Additional Terms for Cataract
  • Now Have Cararacts
  • Cararacts

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Advair Diskus 100/50.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Fluticasone Propionate; Salmeterol Xinafoate

My side effects are hoarse voice and my eye doctor says I have small cataracts in both eyes. Also, I think it has effected my teeth but I'm afraid to go to the dentist because of this....


Source:" Advair Diskus inhalation : User Rating...

View full report on drug related cataract

Did the author experience cataract while taking fluticasone propionate; salmeterol xinafoate?

What is this?

Fluticasone Propionate; Salmeterol Xinafoate

This drug causes the usual fast heart rate, hoarse voice, phlegm production, am a non-smoker. This also delays healing of a cut, increased bleeding tendency and cataract formation which my eye surgeon...


Source:" Advair Diskus inhalation : User Rating...

View full report on drug related cataract

Did the author experience cataract while taking fluticasone propionate; salmeterol xinafoate?

What is this?

Fluticasone Propionate; Salmeterol Xinafoate

Medication works great but I am beginning to question how long I've been using it (over 5 yrs) since I developed cataracts in both eyes, am being watched for glaucoma (pressure in the eye) and osteopo...


Source:" Advair Diskus inhalation : User Rating...

View full report on drug related cataract

Did the author experience cataract while taking fluticasone propionate; salmeterol xinafoate?

What is this?

Tell us about your Experience with Fluticasone Propionate; Salmeterol Xinafoate Related Cataract

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Share Your Experience

Druginformer Identified Side Effects: Dysphonia, Cataract, Fear

Posted By Anonymous in fdb.rxlist.com on April 5, 2013 @ 12:00 am

My side effects are hoarse voice and my eye doctor says I have small cataracts in both eyes. Also, I think it has effected my teeth but I'm afraid to go to the dentist because of this....

Druginformer Identified Side Effects: Dysphonia, Palpitations, Cataract, Haemorrhage

Posted By Hoosier/Buckeye in fdb.rxlist.com on March 8, 2012 @ 12:00 am

This drug causes the usual fast heart rate, hoarse voice, phlegm production, am a non-smoker. This also delays healing of a cut, increased bleeding tendency and cataract formation which my eye surgeon...

Druginformer Identified Side Effects: Osteoporosis, Cataract

Posted By Ess in fdb.rxlist.com on January 8, 2008 @ 12:00 am

... great but I am beginning to question how long I've been using it (over 5 yrs) since I developed cataracts in both eyes, am being watched for glaucoma (pressure in the eye) and osteoporsis and I'm only...



* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.