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Amlodipine (Actavis Pharma): Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Pre Market
Strength:
2.5 mg, 5 mg, 10 mg
ATC code:

Patient Medication Information: uses, side effects, how to take - Amlodipine (Actavis Pharma)

ABOUT THIS MEDICATION

What the medication is used for:

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.

AMLODIPINE can be used by itself or with other medicines to treat these conditions.

What it does:

Amlodipine is a type of medicine known as a calcium channel blocker (CCB).

AMLODIPINE relaxes your blood vessels, which lets your blood flow more easily and helps lower your blood pressure.

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 AMLODIPINE if you:

  • Are allergic to amlodipine (the active ingredient in AMLODIPINE, or to the inactive ingredients listed under “What the nonmedicinal ingredients are” below.
  • Have ever had an allergic reaction to a similar type of drug.
  • 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, Magnesium Stearate, Microcrystalline Cellulose and Sodium Starch Glycolate

What dosage forms it comes in:

AMLODIPINE is available in 3 strengths, namely:

tablets 2.5 mg, 5 mg and 10 mg.

WARNINGS AND PRECAUTIONS

BEFORE you use AMLODIPINE talk to your doctor, nurse or pharmacist if you:

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

    • Are pregnant or plan to become pregnant. AMLODIPINE should not be used during pregnancy unless your doctor tells you otherwise.

    • Are breastfeeding. Do not breast-feed while taking AMLODIPINE.
    • Are older than 65 years.

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 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.

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

INTERACTIONS WITH THIS MEDICATION

As with most medicines, interactions with other drugs are possible. Tell your doctor, nurse or pharmacists about all the medicines you take, including drugs prescribed by other doctors, vitamins, minerals, natural supplements, or alternative medicines. Also mention if you drink alcoholic beverages.

Drug-Drug interaction:

Drugs that may interact with AMLODIPINE include:

  • Cyclosporin
  • Erythromycin, an antibiotic
  • Diltiazem
  • Azole antifungals (e.g. ketoconazole, itraconazole)
  • HIV protease inhibitors (e.g. ritonavir)
  • Beta-blockers
  • Sildenafil (VIAGRA)
  • Statin drugs used to treat high cholesterol (e.g. Simvastatin, Atorvastatin)
  • Tacrolimus (an anti-rejection drug)

Drug-Herb interaction:

  • St-John Wort

Drug-Food interaction:

Do not eat grapefruit or drink grapefruit juice while on AMLODIPINE.

PROPER USE OF THIS MEDICATION

Take AMLODIPINE exactly as prescribed by your doctor, nurse or pharmacist. 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 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:

If you think you have taken too much AMLODIPINE contact your doctor, nurse, pharmacist, 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

Side effects include:

  • Headaches
  • Tiredness, extreme sleepiness
  • Stomach pain, nausea
  • Dizziness
SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effectTalk with your doctor, nurse or pharmacistStop taking drug and seek immediate emergency medical help
Only if severeIn all cases
CommonFlushing: Hot or warm feeling in your face✓
Edema: Swelling of your legs or ankles✓
UncommonArrhythmia: Rapid, slow or irregular heartbeat✓
SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / effectTalk with your doctor, nurse or pharmacistStop taking drug and seek immediate emergency medical help
Only if severeIn all cases
Increased frequency, severity, duration of angina : Pressing or squeezing pain in your chest✓

Heart Attack:

Pain, fullness and/or squeezing of the chest, jaw pain and/or arm pain, shortness of breath

✓
Liver Disorder: Yellowing of the skin or eye, dark urine, abdominal pain, nausea, vomiting, loss of appetite✓
Allergic Reactions: Rash, hives, swelling of the face, lips, tongue or throat, difficulty breathing or swallowing✓
Low Blood Pressure: Dizziness, fainting, lightheadedness. May occur when you go from lying or sitting to standing up✓
Unknown

Extrapyramidal symptoms:

Muscle stiffness, body spasms, upward eye rolling, exaggeration of reflexe, drooling, difficulty moving how and when you want.

✓

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

HOW TO STORE IT

AMLODIPINE should be stored at room temperature between 15 - 30°C. Protect from light and moisture.

Keep AMLODIPINE out of the reach of children.

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 0701E

      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

This document plus the full product monograph, prepared for health professionals can be obtained by contacting the sponsor, Actavis Pharma Company, at: 1-866-254-6111

Last revised: May 12, 2015.

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02433176

Revision date stated in the text: May 12, 2015

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 Amlodipine (Actavis Pharma)

Rx or OTC
Prescription (Rx)?
DIN 02433176, 02433184, 02433192
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 ACTAVIS PHARMA COMPANY
Current status Cancelled Pre Market
Current status date September 1, 2017
Strengths and forms
DIN Strength Dosage form(s) Current status
02433176 2.5 MG Tablet Cancelled Pre Market September 1, 2017
02433184 5 MG Tablet Cancelled Pre Market September 1, 2017
02433192 10 MG Tablet Cancelled Pre Market September 1, 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.