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Losartan Potassium Related Joint Swelling

Official FDA Reports426
Social Media Events4
Active Ingredients
  • Losartan Potassium
Additional Terms for Joint Swelling
  • Swollen Joints
  • Swelling Of Ankles
  • Feet And Ankles Are Swelling
  • Swelling Ankles
  • Swelling In My Legs
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  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Cozaar.


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

Losartan Potassium

did not take losartan for 8 days on vacation,result is swollen ankles ,cold night sweats, extreme fatigue.seeing doctor in. 2 days.


Source:" losartan-hydrochlorothiazide oral : Us...

View full report on drug related joint swelling

Did the author experience joint swelling while taking losartan potassium?

What is this?

Losartan Potassium

... it seemed to work. but in the past 4 months I have dealt with some many side effects that I just want to scream and I want people to know. It caused painful urination, swollen joint , fatigue, rash and ...


Source:" losartan-hydrochlorothiazide oral : Us...

View full report on drug related joint swelling

Did the author experience joint swelling while taking losartan potassium?

What is this?

Cozaar

I have been taking this drug for 3 days and now I have swollen ankles for the past 3 days


Source:" Cozaar Oral : User Ratings covering us...

View full report on drug related joint swelling

Did the author experience joint swelling while taking cozaar?

What is this?

Tell us about your Experience with Losartan Potassium Related Joint Swelling

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Feeling cold, Fatigue, Joint swelling, Night sweats

Posted By big mama in fdb.rxlist.com on March 25, 2014 @ 12:00 am

did not take losartan for 8 days on vacation,result is swollen ankles,cold night sweats, extreme fatigue.seeing doctor in. 2 days.

Druginformer Identified Side Effects: Back pain, Dysuria, Pruritus, Joint swelling, Feeling abnormal, Depression, Dry mouth, Rash, Somnolence, Vision blurred

Posted By Anonymous in fdb.rxlist.com on July 17, 2013 @ 12:00 am

... that I just want to scream and I want people to know. It caused painful urination,swollen joint, fatigue, rash and itching, nasal conjstn, blurry vision,dry mouth,back pain,and bowel troubles. It has ...

Druginformer Identified Side Effects: Joint swelling

Posted By Teresa W. in fdb.rxlist.com on July 23, 2012 @ 12:00 am

I have been taking this drug for 3 days and now I have swollen ankles for the past 3 days

Druginformer Identified Side Effects: Joint swelling, Haemorrhage

Posted By Anonymous in askapatient.com on September 20, 2006 @ 12:00 am

Side Effects: No side effects so far(?) I switched out of plendil because of gum bleeding, raw gums, and perpetually swollen ankles (and besides, it did not reduce my diastolic BP by much. Cozaaar, ...



* 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.