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Cetirizine Hydrochloride Related Heart Rate

Official FDA Reports1
Social Media Events3
Active Ingredients
  • Cetirizine Hydrochloride
Additional Drug Brands and Names
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Additional Terms for Heart Rate
  • Heart Rates
  • Rapid/pounding Pulse

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Zyrtec.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Zyrtec

Anxiety, racing thoughts, head pressure, inability to focus, quickened heart rate . Originally I thought it was my morning coffee that gave me these symptoms, but I've drank two cups e...


Source:" ZYRTEC: Side effects, ratings, and pat...

View full report on drug related heart rate

Did the author experience heart rate while taking zyrtec?

What is this?

Cetirizine Hydrochloride

I had a reaction to cetirizine, racing heart rate and restless. Probably the povidone in it. This was a Member's Mark product purchased at Sam's Club and made in India. Why are they putting povidone i...


Source:" comments/cetirizine/for-allergic-rhini...

View full report on drug related heart rate

Did the author experience heart rate while taking cetirizine hydrochloride?

What is this?

Zyrtec

... which is a drug that basically resets the heartrate and causes extreme chest discomfort. Im now 16 and i've had to go to the emergency room about 5 times since then, my heart rate reaching about 260 b...


Source:" ZYRTEC: Side effects, ratings, and pat...

View full report on drug related heart rate

Did the author experience heart rate while taking zyrtec?

What is this?

Tell us about your Experience with Cetirizine Hydrochloride Related Heart Rate

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Share Your Experience

Druginformer Identified Side Effects: Headache, Anxiety, Heart rate, Disturbance in attention, Tachyphrenia

Posted By Anonymous in askapatient.com on June 6, 2014 @ 12:00 am

Anxiety, racing thoughts, head pressure, inability to focus, quickened heart rate. Originally I thought it was my morning coffee that gave me these symptoms, but I've drank two cups e...

Druginformer Identified Side Effects: Heart rate, Arrhythmia, Restlessness

Posted By Anonymous in drugs.com on November 4, 2009 @ 12:00 am

I had a reaction to cetirizine, racing heart rate and restless. Probably the povidone in it. This was a Member's Mark product purchased at Sam's Club and made in India. Why are they putting povidone i...

Druginformer Identified Side Effects: Chest discomfort, Palpitations, Cardiac flutter, Heart rate

Posted By Anonymous in askapatient.com on October 3, 2007 @ 12:00 am

... was racing 250 beats per minute and i found myself in the emergency room where i was given Adenosine, which is a drug that basically resets the heartrate and causes extreme chest discomfort. Im now 16...



* 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.