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Wolfina

Ingredients: Rauwolfia Serpentina
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Wikipedia

Wolfina is a genus of fungi in the Chorioactidaceae family. There are three species in the genus, found in the USA and China.

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

Tell us about your Experience with Wolfina

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Druginformer Identified Side Effects: None

Posted By offical_kayla_ in twitter.com on June 20, 2014 @ 12:00 am

lol but I wanna know the Wolfina pack 👀

Druginformer Identified Side Effects: None

Posted By offical_kayla_ in twitter.com on June 20, 2014 @ 12:00 am

“ lol but I wanna know the Wolfina pack 👀” u dnt need to knoe us...

Druginformer Identified Side Effects: None

Posted By _JujuBean12 in twitter.com on June 20, 2014 @ 12:00 am

lol but I wanna know the Wolfina pack 👀

Druginformer Identified Side Effects: None

Posted By offical_kayla_ in twitter.com on June 20, 2014 @ 12:00 am

Wolfina's is cuttin up i tell u...

Druginformer Identified Side Effects: None

Posted By offical_kayla_ in twitter.com on June 15, 2014 @ 12:00 am

Wolfina's come as one, u come for one u come for ALL..!!!

Druginformer Identified Side Effects: None

Posted By ThatsRae_ in twitter.com on June 15, 2014 @ 12:00 am

Wolfina's come as one, u come for one u come for ALL..!!!

Druginformer Identified Side Effects: None

Posted By soregananda in twitter.com on June 10, 2014 @ 12:00 am

Wolfina is a fucking H cup oh my god kubo


* 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.