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User Voices for Fluticasone Propionate; Salmeterol Xinafoate

The following are comments from users that experienced side effects while taking Fluticasone Propionate; Salmeterol Xinafoate

Cardiac Flutter

Side Effects: Heart palpitations and coughing. These side affects have been decreasing since I discontinued the drug. Advair seems to be fine for a short time, only to aggravate things later on.


Source: Advair Diskus (Fluticasone / Salmetero...

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

What is this?

Cough

Side Effects: Heart palpitations and coughing . These side affects have been decreasing since I discontinued the drug. Advair seems to be fine for a short time, only to aggravate things later on.


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Contusion

Side Effects: More easy bruising than when not on the medication. This isn't a big deal.

I am able to breath more easily. Taking the medication keeps my airways open and keeps me aliv...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Dry Mouth

Side Effects: I didn't observe any significant side effects aside from a little bit of dry mouth which is alleviated by drinking some water.

Much greater ability to breathe. I ...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Fungal Infection

Side Effects: I have not experienced any treatment side effects. I do have to rinse my mouth out after each dose to prevent oral yeast infection .

Advair keeps my asthma completely in...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Fear

... bouts of extreme fatigue, anxiety and occasional panic attacks that had nothing to do with COPD. Then I started to have choking fits. They were becoming so serious that I feared choking to death. I su...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Panic Attack

... first that they were side effects. I thought that my chronic bronchitis had gotten much worse. Then I began to develop bouts of extreme fatigue, anxiety and occasional panic attacks that had nothing t...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Fatigue

... Effects: I did not realize at first that they were side effects. I thought that my chronic bronchitis had gotten much worse. Then I began to develop bouts of extreme fatigue , anxiety and occasional p...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Decompression Sickness

... had gotten much worse. Then I began to develop bouts of extreme fatigue, anxiety and occasional panic attacks that had nothing to do with COPD. Then I started to have choking fits. They were becoming ...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Anxiety

... I did not realize at first that they were side effects. I thought that my chronic bronchitis had gotten much worse. Then I began to develop bouts of extreme fatigue, anxiety and occasional panic atta...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Hypersomnia

Side Effects: Wallet shock. Patient seems to overall fall asleep easier, but tends to have some problems getting a deep sleep, but this may or may not be related to the Advair. Other than that, the...


Source: Advair Diskus (Fluticasone / Salmetero...

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What is this?

Encephalitis

... Nocardia siriacogeorgensis, MRSA, MAC, aspergillus, pseudomonas among others were all found. the Nocardia in particualr had already caused a mild form of encephalitis .

reduction of a...


Source: Advair Diskus (Fluticasone / Salmetero...

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* 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.