Review: could Amlodipine Besylate cause Withdrawal Syndrome?


Summary

Withdrawal syndrome is found among people who take Amlodipine Besylate, especially for people who are female, 60+ old , have been taking the drug for 6 - 12 months, also take medication Calcium, and have Hypertension . We study 18,889 people who have side effects while taking Amlodipine besylate from FDA and social media. Among them, 11 have Withdrawal syndrome. Find out below who they are, when they have Withdrawal syndrome and more.

You are not alone

Join a support group for people who take Amlodipine besylate and have Withdrawal syndrome >>>

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Amlodipine Besylate

Amlodipine besylate has active ingredients of amlodipine besylate. It is often used in high blood pressure. (latest outcomes from Amlodipine besylate 19,664 users)

Withdrawal Syndrome

Withdrawal syndrome (a discontinuation syndrome is a set of symptoms occurred due to discontinuation of substance) has been reported by people with irritability, drug withdrawal syndrome, agitation, insomnia, sleep disorder (latest reports from 10,442 Withdrawal syndrome patients).

On Aug, 23, 2016

18,889 people reported to have side effects when taking Amlodipine Besylate.
Among them, 11 people (0.06%) have Withdrawal Syndrome


Number of reports submitted per year:

Could Amlodipine besylate cause Withdrawal syndrome?

Time on Amlodipine Besylate when people have Withdrawal Syndrome *:

  • < 1 month: 0.0 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 100 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Withdrawal Syndrome when taking Amlodipine Besylate *:

  • female: 54.55 %
  • male: 45.45 %

Age of people who have Withdrawal Syndrome when taking Amlodipine Besylate *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 16.67 %
  • 50-59: 0.0 %
  • 60+: 83.33 %

Top conditions involved for these people *:

  • Hypertension (6 people)
  • Neuralgia (3 people)
  • Hypothyroidism (2 people)
  • Hypersensitivity (2 people)
  • Anxiety (2 people)

Top co-used drugs for these people *:

  • Calcium (3 people)
  • Seroquel Xr (2 people)
  • Metoprolol Tartrate (2 people)
  • Gabapentin (2 people)
  • Fish Oil (2 people)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Withdrawal syndrome when taking Amlodipine besylate?

Browse all side effects of Amlodipine besylate

a b c d e f g h i j k l m n o p q r s t u v w x y z

Drugs that are associated with Withdrawal syndrome

Withdrawal syndrome

Could your condition cause Withdrawal syndrome

Withdrawal syndrome

Can you answer these questions?

More questions for: Amlodipine besylate, Withdrawal syndrome

You may be interested in these reviews

More reviews for: Amlodipine besylate, Withdrawal syndrome


NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.