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Fluticasone Propionate; Salmeterol Xinafoate Related Drug Effect Increased

Official FDA Reports17
Social Media Events3
Active Ingredients
  • Fluticasone Propionate; Salmeterol Xinafoate
Additional Terms for Drug Effect Increased
  • Worst Side Effects
  • Side Effects Were Not Well Tolerated
  • Got So Many Side Effects
  • Side Effects Far Outweigh Any Benefit
  • Had A Reaction To It
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  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

... this medication, all of those symptoms are gone and my teeth are recovering. Both my Internist and Dentist were unaware that this medication could cause these horrible side effects . I feel so much b...


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

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Did the author experience drug effect increased while taking fluticasone propionate; salmeterol xinafoate?

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Advair Diskus 100/50

Side Effects: terrible side effects , couldn't sleep, really bad muscle cramps in legs & feet, toes would bend back toward ankles, very painful, really painful heartburn, nothing helped. depression c...


Source:" viewrating.asp

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Did the author experience drug effect increased while taking advair diskus 100/50?

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Fluticasone Propionate; Salmeterol Xinafoate

NAMMARIE NEVER HAD A REACTION. IT WAS THE ONLY ONE THAT WORKED THE BEST. FOR ME. BOY IF I WAS A HOUR LATE. I COIULD TELL I FORGOT TO TAKE IT . SORRY U HAD A REACTION TO IT . BUT I GUESS SOMETIMES THAT ...


Source:" forums/copd-discussions/general-suppor...

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Tell us about your Experience with Fluticasone Propionate; Salmeterol Xinafoate Related Drug Effect Increased

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Share Your Experience

Druginformer Identified Side Effects: Fatigue, Myalgia, Disability, Drug effect increased, Muscle spasms

Posted By Carolyn_C in fdb.rxlist.com on March 19, 2014 @ 12:00 am

... filled and after reading the advair reviews listing similar side effects on Web MD, I withdrew from the medication. In addition to the tooth decay, I was chronically exhausted, awakened with severe ...

Druginformer Identified Side Effects: Pain, Depression, Drug effect increased, Dyspepsia, Insomnia, Muscle spasms

Posted By Anonymous in askapatient.com on February 9, 2007 @ 12:00 am

Side Effects: terrible side effects, couldn't sleep, really bad muscle cramps in legs & feet, toes would bend back toward ankles, very painful, really painful heartburn, nothing helped. depression c...

Druginformer Identified Side Effects: Drug effect increased

Posted By slhs3 in mdjunction.com on March 23, 2013 @ 12:00 am

NAMMARIE NEVER HAD A REACTION. IT WAS THE ONLY ONE THAT WORKED THE BEST. FOR ME. BOY IF I WAS A HOUR LATE. I COIULD TELL I FORGOT TO TAKE IT . SORRY U HAD A REACTION TO IT. BUT I GUESS SOMETIMES THAT ...



* 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.