Review: could Ibuprofen cause Intraocular Pressure Increased?


Summary

Intraocular pressure increased is found among people who take Ibuprofen, especially for people who are male, 60+ old , have been taking the drug for < 1 month, also take medication Xalatan, and have Neuralgia . We study 67,448 people who have side effects while taking Ibuprofen from FDA and social media. Among them, 53 have Intraocular pressure increased. Find out below who they are, when they have Intraocular pressure increased and more.

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 >>>

Ibuprofen

Ibuprofen has active ingredients of ibuprofen. It is often used in pain. (latest outcomes from Ibuprofen 92,738 users)

Intraocular Pressure Increased

Intraocular pressure increased has been reported by people with breathing difficulty, hypotension, pain, nausea, glaucoma (latest reports from 8,792 Intraocular pressure increased patients).

On Sep, 20, 2016

67,448 people reported to have side effects when taking Ibuprofen.
Among them, 53 people (0.08%) have Intraocular Pressure Increased


Number of reports submitted per year:

Could Ibuprofen cause Intraocular pressure increased?

Time on Ibuprofen when people have Intraocular Pressure Increased *:

  • < 1 month: 40 %
  • 1 - 6 months: 40 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 20 %

Gender of people who have Intraocular Pressure Increased when taking Ibuprofen *:

  • female: 38 %
  • male: 62 %

Age of people who have Intraocular Pressure Increased when taking Ibuprofen *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 2.27 %
  • 20-29: 0.0 %
  • 30-39: 9.09 %
  • 40-49: 13.64 %
  • 50-59: 15.91 %
  • 60+: 59.09 %

Severity if Intraocular Pressure Increased when taking Ibuprofen **:

  • least: 50 %
  • moderate: 50 %
  • severe: 0.0 %
  • most severe: 0.0 %

Top conditions involved for these people *:

  • Neuralgia (12 people, 22.64%)
  • Hypertension (11 people, 20.75%)
  • Neuropathy Peripheral (8 people, 15.09%)
  • Diabetes Mellitus (8 people, 15.09%)
  • Blood Cholesterol Increased (8 people, 15.09%)

Top co-used drugs for these people *:

  • Xalatan (14 people, 26.42%)
  • Lyrica (13 people, 24.53%)
  • Carvedilol (12 people, 22.64%)
  • Simvastatin (11 people, 20.75%)
  • Glyburide (11 people, 20.75%)

Top other side effects for these people *:

  • Visual Acuity Reduced (14 people, 26.42%)
  • Dizziness (14 people, 26.42%)
  • Vision Blurred (11 people, 20.75%)
  • Gastritis (11 people, 20.75%)
  • Diplopia (11 people, 20.75%)

* 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 Intraocular pressure increased when taking Ibuprofen?

Browse all side effects of Ibuprofen

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 Intraocular pressure increased

Intraocular pressure increased

Could your condition cause Intraocular pressure increased

Intraocular pressure increased

Related studies

Can you answer these questions?

More questions for: Ibuprofen, Intraocular pressure increased

You may be interested in these reviews

More reviews for: Ibuprofen, Intraocular pressure increased


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.