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Proamatine Related Chills

Official Government Database Reports2
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.

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Druginformer Identified Side Effects: Chills, Flushing, Bradycardia, Paraesthesia, Skin disorder

Posted By POTSgrrrrl in drugs.com on October 1, 2010 @ 12:00 am

... below the 50s when I walked a few yards. Bradycardia is a documented side effect, and unfortunately one I suffered from. Also had lots of goosebumps, tingling scalp, chills and flushing throughout t...

Druginformer Identified Side Effects: Pruritus, Chills, Discomfort, Paraesthesia, Skin disorder

Posted By Anonymous in askapatient.com on November 23, 2009 @ 12:00 am

Side Effects: tingly scalp, goosebumps, chills, itchy scalp. The only one that really bothers me is the itchy scalp. It can be embarrassing and very uncomfortable It was a miracle drug fo...

Druginformer Identified Side Effects: Chills, Discomfort, Disturbance in attention, Hot flush, Head deformity

Posted By Anonymous in drugratingz.com on February 28, 2008 @ 12:00 am

it really helped me with circulation and dizziness..it has some side effects that arent terrible just uncomfortable like bad chills,spacey, goosebumps on your scalp, heat flashes,ect. it is just incon...

* 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.