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Amlodipine Besylate Related Asthenia

Official FDA Reports4,209
Social Media Events3
Active Ingredients
  • Amlodipine Besylate
Additional Drug Brands and Names
Additional Terms for Asthenia
  • Loss Of Energy
  • Feeling Weak
  • General Weakness
  • Weakness - General
  • Weakness
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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 Amlodipine.


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

Norvasc

... med I have painful knees hips arm joints lower back pain. I cant get off the floor for the pain it causes. Arms and hands tingling in bed.shoulders aching. General weakness . Leg weakness. Agitation. F...


Source:" NORVASC: Side effects, ratings, and pa...

View full report on drug related asthenia

Did the author experience asthenia while taking norvasc?

What is this?

Amlodipine Besylate

... I went to my doctor for 5mg instead of 10mg, without reason he change to Amlodipine-Benaz 10/20mg sence my b/p has beem high in the morining and very low after meds are taken I feel weak and have a no...


Source:" amlodipine-benazepril Oral : User Rati...

View full report on drug related asthenia

Did the author experience asthenia while taking amlodipine besylate?

What is this?

Norvasc

This medication has lowered my BP, but it has caused leg swelling, loss of energy , confusion, vision problems and shaking inside my body. My Doctor just reduced the Dosage from 10mg. to 7 1/2mg.


Source:" Norvasc Oral : User Ratings covering u...

View full report on drug related asthenia

Did the author experience asthenia while taking norvasc?

What is this?

Tell us about your Experience with Amlodipine Besylate Related Asthenia

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Chest discomfort, Asthenia, Arthralgia, Back pain, Feeling cold, Pain, Agitation, Adverse event, Diabetic diet, Disturbance in attention, Fall, Fluid retention, Paraesthesia, Weight decreased, Weight increased

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

Side Effects: At first chest tightness and tingling in legs, agitation, overly excited,not relaxing. if late taking dose felt weird but hard to explain! Weight loss (good). After a while on this med ...

Druginformer Identified Side Effects: Asthenia

Posted By Nathan in fdb.rxlist.com on December 23, 2009 @ 12:00 am

... I went to my doctor for 5mg instead of 10mg, without reason he change to Amlodipine-Benaz 10/20mg sence my b/p has beem high in the morining and very low after meds are taken I feel weak and have a no...

Druginformer Identified Side Effects: Tremor, Asthenia, Blood pressure decreased, Confusional state, Oedema, Vision blurred

Posted By Patty in fdb.rxlist.com on July 18, 2009 @ 12:00 am

This medication has lowered my BP, but it has caused leg swelling, loss of energy, confusion, vision problems and shaking inside my body. My Doctor just reduced the Dosage from 10mg. to 7 1/2mg.



* 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.