DrugInformer Search


Ingredients: Cidofovir
Average User Review Score
* Based on 0 reviews from across the web.


Read more on Wikipedia

  Please use Workbench for in-depth research on Vistide.

Common adverse events from online conversations
* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

Tell us about your Experience with Vistide

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: None

Posted By InternationalNetworkOnPharmacy... in facebook.com on February 22, 2013 @ 12:00 am

Vistide is indicated for the treatment of cytomegalovirus (CMV) retinitis in patients with acquired immunodeficiency syndrome (AIDS). Vistide is a sterile, hypertonic aqueous solution for intravenous...

Druginformer Identified Side Effects: Initial insomnia, Amnesia

Posted By Anonymous in facebook.com on October 11, 2010 @ 12:00 am

... the four years that followed, I had bronchitis eight months out of the year; I lost my sense of balance; the slightest bit of alcohol made me sick; I had increasing trouble falling asleep; and I could...

Druginformer Identified Side Effects: None

Posted By Anonymous in facebook.com on November 15, 2009 @ 12:00 am

Terri Herbs did nothing for me. I tried acupuncture for well over 1 year with no results. My integrative medicine doctor said I was too sick to bother with herbs or supplements so he wanted to bring o...

Druginformer Identified Side Effects: None

Posted By Anonymous in eu-es.facebook.com

Ted A company that delivered contaminated vaccines with live avian flu and human flu viruses earlier this year is now to lead the charge for designing vaccines for the Mexican Swine Flu outbreak. Ac...

* 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.