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Jamp Olmesartan: Uses, Side Effects and Dosage

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Facts
Status:
Prescription (Rx)
Strength:
20 mg, 40 mg
Active ingredient:

Patient Medication Information: uses, side effects, how to take - Jamp Olmesartan

What is JAMP Olmesartan used for?

JAMP Olmesartan is an angiotensin receptor blocker (ARB) used to lower blood pressure in adults and children above 6 years old.

High blood pressure increases the workload of the heart and arteries. If this condition continues for a long time, damage to the blood vessels of the brain, heart, and kidneys can occur, and may eventually result in a stroke, heart or kidney failure. High blood pressure also increases the risk of heart attacks. Reducing your blood pressure decreases your risk of developing these illnesses.

How does JAMP Olmesartan work?

JAMP Olmesartan contains a drug olmesartan medoxomil which is a drug that prevents the hormone in your body that causes the blood vessels to constrict. JAMP Olmesartan lowers blood pressure by relaxing your blood vessels.

JAMP Olmesartan does not cure your high blood pressure. It helps to control it. Therefore, it is important to continue taking JAMP Olmesartan regularly even if you feel fine.

What are the ingredients in JAMP Olmesartan?

Medicinal ingredients: Olmesartan medoxomil

Non-medicinal ingredients: Colloidal silicon dioxide, hydroxy propyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, talc, titanium oxide.

Serious Warnings and Precautions

JAMP Olmesartan should not be used during pregnancy. Taking JAMP Olmesartan during pregnancy can cause harm and even death to your baby. If you discover that you are pregnant while taking JAMP Olmesartan, stop the medication as soon as possible and contact your doctor.

JAMP Olmesartan comes in the following dosage forms:

20 mg and 40 mg.

Do not use JAMP Olmesartan if:

  • are allergic to Olmesartan medoxomil or to any of the other ingredients of JAMP Olmesartan.
  • have experienced an allergic reaction with swelling of the hands, feet, or ankles, face, lips, tongue, throat, or sudden difficulty breathing or swallowing, to any ARB (You can recognize an ARB because its medicinal ingredient ends in “-SARTAN”). Be sure to tell your doctor, nurse, or pharmacist that this has happened to you.
  • are pregnant or intend to become pregnant. If this is the case, talk to your doctor as soon as possible. Taking JAMP Olmesartan during pregnancy can cause harm and even death to your baby.
  • are breastfeeding. It is possible that JAMP Olmesartan passes into breast milk.
  • have diabetes or kidney disease and are already taking a medicine that contains aliskiren (such as Rasilez), used to lower high blood pressure.

JAMP Olmesartan is not recommended for use in children below the age of 6 years.

To help avoid side effects and ensure proper use, talk to your healthcare professional before you take JAMP Olmesartan. Talk about any health conditions or problems you may have, including if you:

  • have experienced an allergic reaction to any drug used to lower blood pressure.
  • have a narrow heart valve or arteries.
  • had a heart attack or have heart or blood vessel disease.
  • had a stroke or have a condition that affects the blood supply to the brain.
  • have, liver or kidney disease.
  • have blocked bile ducts.
  • have diabetes.
  • are dehydrated or suffer from excessive vomiting, diarrhea, or sweating.
  • are on a low-salt diet.
  • are taking a salt substitute that contains potassium, potassium supplements, or a potassium-sparing diuretic (a specific kind of “water pill” that makes your body keep potassium).
  • are taking a medicine that contains aliskiren, such as Rasilez, used to lower high blood pressure.
  • are taking an angiotensin converting enzyme inhibitor (ACE Inhibitors). You can recognize ACE Inhibitors because their medicinal ingredient ends in “-PRIL”.
  • are less than 18 years old or the drug is for your child.

Other warnings you should know about:

JAMP Olmesartan can prevent the normal growth of your baby’s kidneys and skull if you take the drug during the second and third trimester. Your doctor may recommend an ultrasound.

JAMP Olmesartan can cause severe chronic diarrhea with substantial weight loss (sprue-like enteropathy). It can take months to years for symptoms to develop.

Driving and using machines: Before you perform tasks which may require special attention, wait until you know how you respond to JAMP Olmesartan. Dizziness, lightheadedness, or fainting can occur when you take the drug for the first time and when your dosage is increased.

Tell your healthcare professional about all the medicines you take, including any drugs, vitamins, minerals, natural supplements or alternative medicines.

The following may interact with JAMP Olmesartan:

  • Agents increasing serum potassium, such as a salt substitute that contains potassium, potassium supplements, or a potassium-sparing diuretic (a specific kind of “water pill”).
  • Blood pressure lowering drugs, including diuretics (“water pills”), aliskiren-containing products (e.g. Rasilez), or angiotensin converting enzyme inhibitors (ACE Inhibitors).
  • Diuretics.
  • Lithium used to treat bipolar disease.
  • Nonsteroidal anti-inflammatory drugs (NSAIDs), used to reduce pain and swelling. Examples include ibuprofen, naproxen, and celecoxib (COX-2 Inhibitor).

How to take JAMP Olmesartan:

  • JAMP Olmesartan may be taken with or without food.

  • Take exactly as directed by your Doctor. Do NOT take more of it than prescribed.

Usual dose:

For adult patients:

  • 20 mg tablet once daily.
  • Can be increased to 40 mg by your doctor if your blood pressure is not well controlled after two weeks of treatment.

For pediatric patients age (6 to 16 years old):

Weight between 20 kg to less than 35 kg:

  • 10 mg once daily.
  • Can be increased to 20 mg once daily by the doctor if blood pressure is not well controlled after two weeks of treatment.

Weight of 35 kg or more:

  • 20 mg once daily.
  • Can be increased to 40 mg once daily if blood pressure is not well controlled after two weeks of treatment.

Overdose:

If you think you, or a person you are caring for, have taken too much JAMP Olmesartan, contact your healthcare professional, hospital emergency department or regional poison control centre immediately, even if there are no symptoms.

Missed Dose:

If you have forgotten to take your dose during the day, carry on with the next one at the usual time. Do not double dose.

What are possible side effects from using JAMP Olmesartan?

These are not all the possible side effects you may feel when taking JAMP Olmesartan. If you experience any side effects not listed here, contact your doctor.

Any medicine may have unintended or undesirable effects, so-called side effects.

Side effects may include:

  • Back pain
  • Decreased appetite
  • Dizziness and headache
  • Gastrointestinal problems

    • Constipation
    • Diarrhea
    • Nausea
    • Upset stomach
    • Vomiting
  • Joint pain
  • Muscle cramps, spasms and pain
  • Rash, red itchy patches on skin
  • Restlessness and weakness
  • Upper respiratory infection

    • Congested and runny nose
    • Cough
    • Sore throat

JAMP Olmesartan can cause abnormal blood test results. Your doctor will decide when to perform blood tests and will interpret the results.

Serious side effects and what to do about them

Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
COMMON

Low Blood Pressure:

dizziness, fainting, lightheadedness.

√
Bronchitis: shortness of breath, weakness, high fever, coughing, fatigue, wheezing or whistling sound when breathing.√
Hematuria (blood in urine): pink, red or very dark urine.√
UNCOMMON
Ear Disorder (Vertigo): a sense of dizziness, spinning.√
Tachycardia (abnormally fast heartbeat): dizziness, light headedness, shortness of breath, racing heart.√

Serious side effects and what to do about them

Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
Hyperuricaemia (Increased levels of uric acid in the blood): swelling and redness in the joints.√
Chest Pain: Pressure or tightness in your chest√
Edema: unusual swelling of the arms, hands, legs, feet and ankles.√
Kidney Disorder: change in frequency of urination, nausea, vomiting, swelling of extremities, fatigue.√
Liver Disorder: yellowing of the skin or eyes, dark urine, abdominal pain, nausea, vomiting, loss of appetite.√
RARE
Acute Kidney Failure: decrease or absence of urine, generalized swelling, weakness, shortness of breath, or irregular heartbeats, loss of appetite, lethargy and fatigue.√

Allergic Reaction:

rash, hives, swelling of the face, lips, tongue or throat, difficulty swallowing or breathing.

√
Rhabdomyolysis (breakdown of damaged muscles): muscle pain that you cannot explain, muscle tenderness or weakness, dark brown urine.√

Increased Levels of Potassium in the Blood:

irregular heartbeats, muscle weakness and generally feeling unwell.

√
UNKNOWN

Sprue-like Enteropathy:

severe chronic diarrhea with substantial weight loss.

√

If you have a troublesome symptom or side effect that is not listed here or becomes bad enough to interfere with your daily activities, tell your healthcare professional.

Reporting Side Effects

You can report any suspected side effects associated with the use of health products to Health Canada by:

  • Visiting the Web page on Adverse Reaction Reporting (https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect- canada/adverse-reaction-reporting.html) for information on how to report online, by mail or by fax; or
  • Calling toll-free at 1-866-234-2345.

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

Storage:

Blister pack: The tablets should be stored at 15°C –30°C.

Bottle: The tablets should be stored at 15°C –30°C. Protect from moisture.

Keep out of sight and reach of children and pets.

If you want more information about JAMP Olmesartan:

  • Talk to your healthcare professional
  • Find the full product monograph that is prepared for healthcare professionals and includes this Patient Medication Information by visiting the Health Canada website (https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database.html)or the JAMP Pharma Corporation website (www.jamppharma.com) or by calling at 1-866-399-9091.

JAMP Pharma Corporation

1310 rue Nobel

Boucherville, Quebec

J4B 5H3, Canada

Last revised: October 26, 2021

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02461641

Revision date stated in the text: October 26, 2021

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Jamp Olmesartan

Rx or OTC
Prescription (Rx)?
DIN 02461641, 02461668
Schedule(s) PRESCRIPTION
Active ingredient(s) Olmesartan medoxomil
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. C Cardiovascular system drugs
    1. C09 Agents acting on the renin-angiotensin system
      1. C09C Angiotensin II receptor blockers (ARBs), plain
        1. C09CA Angiotensin II receptor blockers (ARBs), plain
          1. C09CA08 Olmesartan medoxomil
Company JAMP PHARMA CORPORATION
Current status Marketed
Current status date October 28, 2021
Strengths and forms
DIN Strength Dosage form(s) Current status
02461641 20 MG Tablet Marketed October 28, 2021
02461668 40 MG Tablet Marketed October 28, 2021

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.