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User Voices for Cevimeline Hydrochloride

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

Drug Ineffective

... all. If that wasn't bad enough I have severe burning in my lips I have to apply an Rx. ointment 10-15 times a day.Can this be reversed? The ointment is for yhe burning, does nothing for the dryness. I...


Source: Evoxac Oral : User Ratings covering us...

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Drug Ineffective

Pill 3X/day; 3 months on, 6 months off, 3 months on again as a second trial to test it's effectiveness on dry mouth. Result: no effect whatsoever .


Source: Evoxac Oral : User Ratings covering us...

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Drug Ineffective

I have used this drug for several years.It causes me to sweat but it does not help the dry mouth and eyes very much. I have also started to shake in my hands. So much that I couldn't get a spoon in m...


Source: Evoxac Oral : User Ratings covering us...

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Drug Ineffective

Didn't work well taking two 30mg a day but three times a day worked better.


Source: Evoxac Oral : User Ratings covering us...

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Drug Ineffective

I have it. I 've had punctal plugs and used evoxac with no help . I actually find that contact lenses help me during the day- I can't stand air coming in contact with my eyes. I get abraisions all the ...


Source: FibroColors/posts/153855088105651

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Drug Ineffective

They help get the word out. Advertising? Not sure how , if you feel the drug isn't working for you or too many side effects. Cancer patients also use this drug. I know we have some users he...


Source: Sjogren's Syndrome General Discussions...

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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.