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User Voices for Pyrithione Zinc

The following are comments from users that experienced side effects while taking Pyrithione Zinc

Pruritus

Not convinced one way or another In the winter, my scalp tends to get a tad dry and itchy . Normally, I don't do much about it and simply wait for the winter to end. This year I decided to do somethi...


Source: Selsun Blue Naturals Featured Review

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Dandruff

Dandruff Control - Yeah right! I have tried so many different dandruff shampoos that are on the market it is rediculous and I am still searching for the one that does as it promises. It seems like no ...


Source: Selsun Blue Naturals Featured Review

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Burning Sensation

As I snapped closed the lid to the dandruff shampoo which contained Pyrithione Zinc , the shampoo that was under the cap had shut directly in my eye causing immediate burning . I tried rinsing and rinsi...


Source: comments/pyrithione-zinc-topical/for-d...

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Eye Swelling

... a,but it was so hard to get my eye open. Once I took out my contact lense, the burning intensified. I went to bed that evening and awoke 2 hours later with severe pain, eye was swollen and closed shut ...


Source: comments/pyrithione-zinc-topical/for-d...

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Pain

... and rinsing a,but it was so hard to get my eye open. Once I took out my contact lense, the burning intensified. I went to bed that evening and awoke 2 hours later with severe pain ,eye was swollen and ...


Source: comments/pyrithione-zinc-topical/for-d...

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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.