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Sandoz Clonidine (Sandoz Canada, 0.025 mg): Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
0.025 mg
Active ingredient:
ATC code:

Patient Medication Information: uses, side effects, how to take - Sandoz Clonidine (Sandoz Canada, 0.025 mg)

ABOUT THIS MEDICATION

What the medication is used for:

Sandoz Clonidine Tablets are used to provide relief from hot flushes that may occur in women at menopause (change of life).

What it does:

Sandoz Clonidine Tablets helps reduce the frequency, severity and duration of menopausal flushing (due to decreased estrogen levels).

When it should not be used:

Do not take this medicine if:

  • You are allergic to clonidine hydrochloride or any other ingredients in Sandoz Clonidine or have a rare hereditary problem of galactose intolerance or the Lapp lactose deficiency. Sandoz Clonidine contains lactose.
  • You have a severe slow heart rate; Sandoz Clonidine can lower the heart and pulse rate.

What the medicinal ingredient is:

clonidine hydrochloride.

What the important nonmedicinal ingredients are:

The Sandoz Clonidine (clonidine hydrochloride) tablet core contains the following inactive ingredients: Povidone, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate.

The Sandoz Clonidine tablet coating contains FD&C Blue #2, hypromellose, polyethylene glycol, polyvinyl alcohol - partially hydrolyzed, talc and titanium dioxide.

What dosage forms it comes in:

Sandoz Clonidine is available in tablets. Each tablet contains 0.025 mg of clonidine hydrochloride.

WARNINGS AND PRECAUTIONS

BEFORE you use Sandoz Clonidine talk to your doctor or pharmacist about any health conditions or problems you may have, including if you:

  • have low blood pressure;
  • have a slow heart rate, or heart failure, or irregular
  • heart rate, or a recent heart attack;
  • have or have had a stroke;
  • have poor blood circulation to hands and feet such as

    • Raynaud’s syndrome;
    • are suffering from constipation;
    • have kidney disease;
    • have eye problems such as dry eye or wear contact lenses;
    • have or have had depression;
    • are pregnant or planning to become pregnant;

    • are breast-feeding.

Sandoz Clonidine is not to be used in patients under 18 years of age.

Sandoz Clonidine may cause sleepiness, dizziness and fainting. Do not drive or operate machinery until you know how the drug affects you.

INTERACTIONS WITH THIS MEDICATION

Tell your doctor or pharmacist all the medicines you are taking including all prescription, non-prescription and natural health products, particularly if you are taking the following medicines:

  • drugs that contain clonidine
  • drugs that lower blood pressure such as water pills, betablockers, vasodilators, calcium antagonists, ACE-inhibitors
  • drugs that slow the heart rate
  • drugs for depression and MAO inhibitors
  • alpha2 receptor blockers such as phentolamine
  • methylphenidate
  • indomethacin and other non-steroidal antiinflammatory agents
  • barbiturates or other sedatives, including alcohol

PROPER USE OF THIS MEDICATION

Follow your doctor’s instructions about when and how to take your medicine and always read the label.

Usual dose:

0.05 mg (two 0.025 mg tablets) twice a day. The tablets should be swallowed whole with water.

Do not stop taking Sandoz Clonidine without talking to your doctor since stopping Sandoz Clonidine suddenly may cause a severe withdrawal reaction, which in rare cases can cause death.

Overdose:

If you think you have taken too much Sandoz Clonidine, contact your healthcare professional, hospital emergency department or regional poison control centre immediately, even if there are no symptoms.

Missed Dose:

If you forget to take a dose take one as soon as you remember, then carry on as before.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Side effects may include: dry mouth, dizziness, tiredness, headache, nausea, vomiting, constipation, feeling weak (malaise), sleepiness, drowsiness and erectile dysfunction (trouble getting or keeping an erection), itchiness, rash, hive, hair loss.

If you experience any of these effects or any other effects not mentioned above and they continue or become troublesome, talk to your doctor or pharmacist.

Sandoz Clonidine can cause abnormal blood test results. Sandoz Clonidine may also increase blood sugar, you may need to test your blood sugar more often.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN 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

Blood pressure

effects: Fall in blood pressure on standing

√
Urinary effects: Urinary difficulty or retention√
UncommonAllergic reaction: Hives, swelling of lips, face or throat with difficulty breathing or speaking (signs of angioedema)√
Hypersensitivity reactions: Skin rash, skin eruption or other effect on the skin or eyes√
Muscle or joint effects: Muscle or joint pain and cramps of the lower limbs√

Hallucination:

Problem with circulation to the fingers and toes (Raynaud’s pheonomenon)

√
RareHeart effects: Racing or irregular heart rate, slow heart rate√
Blockage of the large bowel: Colicky pain, constipation, vomiting, liver problems√

Liver disorder:

Symptoms such as nausea, vomiting, dark/brown urine

√
Not KnownConfusion state√
SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effectTalk to your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases
Disability of the eye to change its focus from near to distant objects√

This is not a complete list of side effects. For any unexpected effects while taking Sandoz Clonidine, contact your doctor or pharmacist.

HOW TO STORE IT

The tablets should not be taken after the expiry date which is printed on the label.

Sandoz Clonidine Tablets should be stored at room temperature (15°C - 30°C). Protect from moisture.

Keep this medicine out of the sight and reach of children.

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.

MORE INFORMATION

If you want more information about Sandoz Clonidine:

  • 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://health-products.canada.ca/dpd-bdpp/index-eng.js); the manufacturer’s website (www.sandoz.ca), or by calling 1-800-361-3062.

Last Prepared: May 20, 2021.

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02516217

Revision date stated in the text: May 20, 2021

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

Drug information for Sandoz Clonidine (Sandoz Canada, 0.025 mg)

Rx or OTC
Prescription (Rx)?
DIN 02516217
Schedule(s) PRESCRIPTION
Active ingredient(s) Clonidine hydrochloride 0.025 MG
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. C Cardiovascular system drugs
    1. C02 Antihypertensives
      1. C02A Antiadrenergic agents, centrally acting
        1. C02AC Imidazoline receptor agonists
          1. C02AC01 Clonidine
Company SANDOZ CANADA INCORPORATED
Current status Marketed
Current status date February 2, 2022

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.