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Q-Gen Amlodipine: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled (Unreturned Annual)
Strength:
5 mg, 10 mg
ATC code:

Patient Medication Information: uses, side effects, how to take - Q-Gen Amlodipine

ABOUT THIS MEDICATION

What the medication is used for:

Q-GEN AMLODIPINE has been prescribed to you for:

  • The treatment of high blood pressure (hypertension), or
  • The management of a type of chest pain called angina. Q-GEN AMLODIPINE can be used by itself or with other medicines to treat these conditions.

What it does:

Q-GEN AMLODIPINE is a type of medicine known as a calcium channel blocker (CCB).

Q-GEN AMLODIPINE relaxes your blood vessels, which lets your blood flow more easily and helps lower your blood pressure. Q-GEN AMLODIPINE controls chest pain by improving the supply of blood and oxygen to the heart and by reducing its workload.

When it should not be used:

Do not use Q-GEN AMLODIPINE if:

  • You are allergic to amlodipine (the active ingredient in Q-

    Gen-Amlodipine), or to the inactive ingredients listed under “What the nonmedicinal ingredients are” below.

  • You have ever had an allergic reaction to a similar type of

    drug.

  • You have very low blood pressure (less than 90 mmHg

    systolic).

What the medicinal ingredient is:

Amlodipine besylate

What the nonmedicinal ingredients are:

Dibasic calcium phosphate anhydrous, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

What dosage forms it comes in:

Tablets 5 mg and 10 mg amlodipine (as amlodipine besylate).

WARNINGS AND PRECAUTIONS

BEFORE you use Q-GEN AMLODIPINE talk to your doctor or pharmacist if:

  • You ever had heart or blood vessel diseases.
  • You have aortic stenosis (narrowing of a valve of your heart).
  • You have liver or kidney problems.

    • You have very low blood pressure (less than 90 mmHg systolic).
    • You are pregnant, or plan to become pregnant.

      Q-GEN AMLODIPINE should not be used during pregnancy unless your doctor tells you otherwise.

    • You are breast-feeding. Do not breast-feed while taking Q-

      Gen-Amlodipine

    • You are older than 65 years.

Q-GEN AMLODIPINE may occasionally cause low blood pressure (hypotension). Your blood pressure should be carefully monitored, especially if you have had a stroke or take other drugs to lower your blood pressure.

If you take Q-GEN AMLODIPINE together with a drug known as beta-blockers (e.g. acebutolol, atenolol, metoprolol, nadolol), do not suddenly stop using the beta-blocker. If your doctor advises you to discontinue use of the beta-blocker, your dose should be decreased slowly, as recommended by your doctor, before stopping it completely.

Q-GEN AMLODIPINE is not recommended for use in children less than 6 years of age.

INTERACTIONS WITH THIS MEDICATION

Tell your doctor or pharmacists about all drugs you are taking including prescription, non-prescription medicines and natural or herbal remedies. Also mention if you drink alcoholic beverages or use drugs.

Drugs that may interact with Q-GEN AMLODIPINE include:

  • Erythromycin, an antibiotic
  • Diltiazem
  • Azole antifungals (e.g. ketoconazole, itraconazole)
  • HIV protease inhibitors (e.g. ritonavir)
  • St John's wort
  • Beta-blockers
  • Sildenafil (VIAGRA)

Do not eat grapefruit or drink grapefruit juice while on Q-Gen-Amlodipine

PROPER USE OF THIS MEDICATION

Take Q-GEN AMLODIPINE exactly as prescribed by your physician. It may be easier to take your dose if you do it at the same time every day, such as with breakfast or dinner, or at bedtime. Do not stop taking your medication without having first informed your doctor.

Usual dose:

For both high blood pressure and chest pain, the recommended initial dose of Q-GEN AMLODIPINE is 5 mg once daily. If necessary, your doctor may increase your dose to a maximum dose of 10 mg once daily.

Use in Patients with liver disease:

The starting dose is 2.5 mg once daily and can be gradually increased by your doctor.

Use in Children (6-17 years old):

The recommended dose is 2.5 mg to 5 mg once daily.

Overdose:

In case of drug overdose, contact a health care practitioner, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

One or more of the following signs may occur in an overdose: Low blood pressure and rapid heartbeat.

Missed Dose:

If you miss a dose, take it as soon as you remember. If it has been more than 12 hours since you missed your last dose, skip the missed dose and continue with the next dose at your regular time. Do not take double doses.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Along with its intended action, any medication may cause undesirable effects. The most common side effects of Gen amlodipine include swelling (edema) and headaches.

However, check with your doctor or pharmacist promptly if any of the following persist or become troublesome:

  • Tiredness, extreme sleepiness
  • Stomach pain, nausea
  • Dizziness

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND

WHAT TO DO ABOUT THEM

Symptom / effect

Talk with your

doctor or pharmacist

Stop taking drug and call your doctor or pharmacist
Only if severeIn all cases
Common

Flushing (hot or warm

feeling in your face)

U
Swelling of your legs or anklesU
UncommonArrhythmia (Rapid, slow or irregular heartbeat)U

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND

WHAT TO DO ABOUT THEM

Increased

frequency,

severity,

duration of

angina

(pressing or squeezing pain in your chest) or heart attack Jaundice

(yellowing of the skin or eye, dark urine,

nausea &

vomiting, loss of appetite)

Allergic

reactions (rash, hives, swelling of the face, throat, lips, difficulty

breathing or swallowing)

Talk with your doctor or pharmacist
U
U
UU

This is not a complete list of side effects. For any unexpected effects while taking Q-Gen-Amlodipine, contact your doctor or pharmacist.

HOW TO STORE IT

Keep Q-GEN AMLODIPINE out of the reach and sight of children. Store Q-GEN AMLODIPINE Tablets at room temperature (between 15-30°C). Protect Q-GEN AMLODIPINE from light .

REPORTING SUSPECTED SIDE EFFECTS

You can report any suspected adverse reactions associated with the use of health products to the Canada Vigilance Program by one of the following 3 ways:

--------------------------------------------------------------------------

  • Report online at www.healthcanada.gc.ca/medeffect
  • Call toll-free at 1-866-234-2345
  • Complete a Canada Vigilance Reporting Form and:

    • Fax toll-free to 1-866-678-6789, or
    • Mail to: Canada Vigilance Program Health Canada

      Postal Locator 0701D

      Ottawa, Ontario

      K1A 0K9

Postage paid labels, Canada Vigilance Reporting Form and the adverse reaction reporting guidelines are available on the MedEffect™ Canada Web site at www.healthcanada.gc.ca/medeffect.

NOTE: Should you require information related to the management of side effects, contact your health professional. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

Last revised: October 30, 2011

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02375222

Revision date stated in the text: October 30, 2011

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 Q-Gen Amlodipine

Rx or OTC
Prescription (Rx)?
DIN 02375222, 02375230
Schedule(s) PRESCRIPTION
Active ingredient(s) Amlodipine (amlodipine besylate)
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. C Cardiovascular system drugs
    1. C08 Calcium channel blockers
      1. C08C Selective calcium channel blockers with mainly vascular effects
        1. C08CA Dihydropyridine derivative selective calcium channel blockers with mainly vascular effects
          1. C08CA01 Amlodipine
Company Q-GEN PHARMACEUTICALS INC
Current status Cancelled (Unreturned Annual)
Current status date September 5, 2017
Strengths and forms
DIN Strength Dosage form(s) Current status
02375222 5 MG Tablet Cancelled (Unreturned Annual) September 5, 2017
02375230 10 MG Tablet Cancelled (Unreturned Annual) September 5, 2017

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.