Does Zyrtec cause dementia?
Long-term use of Benadryl, an over-the-counter allergy medication, has been linked to an increased dementia risk.
In lieu of Benadryl, possible alternatives include cetirizine (Zyrtec), fexofenadine (Allegra) and loratadine (Claritin)..
What are the side effects of long term use of Zyrtec?
That said, Cetirizine can cause adverse effects, such as:some drowsiness.excessive tiredness.dry mouth.stomach pain.diarrhea.vomiting.
Is Zyrtec being recalled?
According to the most recent FDA Enforcement Report, Perrigo is recalling 14 batches of its private label version of Zyrtec. That amounts to 209,256 cartons of blister packs of cetirizine HCl 10-mg tablets.
Why is Zyrtec recalled?
Sandoz issued a voluntary recall of 1,023,430 units of Zyrtec (10 mg) capsules as a result of failed impurities and a specification being reported for impurity at the 21 month stability time point, according to an FDA Enforcement Report.
Does Zyrtec raise blood pressure?
For allergy sufferers with heart disease, medicines such as Allegra, Zyrtec or Claritin should be safe. However, medicines containing decongestants — including Allegra-D, Zyrtec-D and Claritin-D — could increase your blood pressure and heart rate or interfere with your heart medication.
Can Zyrtec cause numbness?
numbness, tingling, burning pain; decreased sense of taste; headache; upset stomach, nausea, constipation; or.
Does Drugs affect your memory?
Drug abuse is a serious factor in memory loss and a lack of concentration, which can affect aspects of your life you may not have considered. Drugs can make it hard for you to study, improve your skills at work, learn and retain new concepts, and even pay attention to what’s happening around you.
Do all antihistamines cause dementia?
But there was no association between dementia and antihistamine medications. A 2018 study had similar findings. While certain types of anticholinergic medications were linked to dementia, antihistamines were not.
Why was Zyrtec taken off the market?
According to the June 26, 2019, US Food and Drug Administration (FDA) Enforcement Report, P & L Developments initiated the recall after learning of a recall issued by its supplier over potential Burkholderia cepacia (B. cepacia) and Ralstonia pickettii (R. pickettii) contamination.