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Albuterol Related Hypertension

Official Government Database Reports1,125
Online Conversations6

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: Erythema, Hypersensitivity, Heart rate increased, Chest pain, Hypertension, Rash

Posted By Anonymous in askapatient.com on January 27, 2012 @ 12:00 am

Side Effects: immediate chest pain, bright red rash all over face, raised my pulse rate by 10, raised my BP from 115/60 to 150/65 looks like mine was an allergic reaction to this drug

Druginformer Identified Side Effects: Heart rate increased, Hypertension

Posted By restoredhope in www.dailystrength.org

Was taking both nebulizer and rescue inhaler every two hours DAILY. It did help at times. Hated the rapid heart rate and elevated blood pressure.

Druginformer Identified Side Effects: Hypertension

Posted By JazmineK in www.dailystrength.org

Creates hypertensio

Druginformer Identified Side Effects: Nervousness, Drug intolerance, Hypertension

Posted By Aqualung55 in www.dailystrength.org

Made me very nervous; increased BP and HR. Couldn't tolerate it and had no real improvement.

Druginformer Identified Side Effects: Feeling jittery, Hypertension, Psychomotor hyperactivity

Posted By MsSmiles in www.dailystrength.org

Made me extremely too hyper and jittery. Caused blood pressure to rise rapidly.

Druginformer Identified Side Effects: Dry mouth, Hypertension

Posted By marguerit in www.dailystrength.org

works, raises my blood pressure and gives me dry mouth

* 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.