Repreve Side Effects


Common Repreve Side Effects

The most commonly reported Repreve side effects (click to view or check a box to report):

International Normalised Ratio Increased (1)
Intraocular Pressure Increased (1)
Hypoglycaemia (1)
Glaucoma (1)
Eye Pain (1)
Blood Glucose Decreased (1)

If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Repreve Side Effects Reported to FDA

Repreve Side Effect Report#5426210-2
Blood Glucose Decreased, Hypoglycaemia, International Normalised Ratio Increased
This is a report of a 75-year-old male patient (weight: NA) from Australia, suffering from the following health symptoms/conditions: NA, who was treated with Repreve (dosage: .25mg Per Day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Blood Glucose Decreased, Hypoglycaemia, International Normalised Ratio Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Repreve treatment in male patients, resulting in Blood Glucose Decreased side effect.
Repreve Side Effect Report#5283209-7
Eye Pain, Glaucoma, Intraocular Pressure Increased
This report suggests a potential Repreve Eye Pain side effect(s) that can have serious consequences. A 56-year-old female patient (weight: NA) from Australia was diagnosed with the following symptoms/conditions: restless legs syndrome,depression and used Repreve (dosage: .25mg Per Day) starting NS. After starting Repreve the patient began experiencing various side effects, including: Eye Pain, Glaucoma, Intraocular Pressure IncreasedAdditional drugs used concurrently:
  • Lexapro (10mg Per Day)
  • Metformin (1g Three Times Per Day)
  • Tibolone (2.5mg Per Day)
  • Pantoprazole Sodium (40mg Per Day)
Although Repreve demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eye Pain, may still occur.

The appearance of Repreve on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Repreve Side Effects for Women?

Women Side EffectsReports
Eye Pain 1
Glaucoma 1
Intraocular Pressure Increased 1

What are common Repreve Side Effects for Men?

Men Side EffectsReports
Blood Glucose Decreased 1
Hypoglycaemia 1
International Normalised Ratio Increased 1

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Repreve reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Repreve Safety Alerts, Active Ingredients, Usage Information

    More About Repreve

    Side Effects reported to FDA: 2

    Repreve safety alerts: No

    Latest Repreve clinical trials