Inderal 40mg Tablets

Manufacturer WYETH Active Ingredient Propranolol Tablets(proe PRAN oh lole) Pronunciation proe PRAN oh lole
It is used to treat high blood pressure.It is used to treat chest pain or pressure. It is used to help certain heart problems.It is used to prevent migraine headaches.It is used to treat tremor (essential).It is used after a heart attack to help prevent future heart attacks and lengthen life.It is used to treat pheochromocytoma. It is used to treat certain types of abnormal heartbeats.
đŸˇī¸
Drug Class
Antihypertensive, Antiarrhythmic, Antianginal, Migraine Prophylaxis
đŸ§Ŧ
Pharmacologic Class
Non-selective beta-adrenergic blocker
🤰
Pregnancy Category
Category C
✅
FDA Approved
Nov 1967
âš–ī¸
DEA Schedule
Not Controlled

Overview

â„šī¸

What is this medicine?

Propranolol is a type of medicine called a beta-blocker. It works by relaxing blood vessels and slowing your heart rate, which helps to lower blood pressure, relieve chest pain (angina), prevent migraines, and treat certain heart rhythm problems. It can also help with tremors and anxiety.
📋

How to Use This Medicine

Taking Your Medication Correctly

To ensure you get the most benefit from your medication, follow these guidelines:

Take your medication exactly as directed by your doctor.
Read all the information provided with your medication and follow the instructions carefully.
Some medications should be taken with food, while others should be taken on an empty stomach. If you're unsure, consult with your pharmacist for guidance.

It's essential to continue taking your medication as prescribed by your doctor or healthcare provider, even if you start to feel better.

Storing and Disposing of Your Medication

To maintain the effectiveness and safety of your medication:

Store it at room temperature, avoiding freezing temperatures.
Protect the medication from heat, cold, and light sources.
Keep the container lid tightly closed when not in use.

What to Do If You Miss a Dose

If you miss a dose, take the following steps:

Take the missed dose as soon as you remember.
If it's close to the time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule.
* Do not take two doses at the same time or take extra doses to make up for the missed one.
💡

Lifestyle & Tips

  • Do not stop taking this medication suddenly, especially if you have heart disease. Your doctor will tell you how to slowly reduce the dose over time.
  • Take your medication exactly as prescribed. Do not skip doses.
  • Monitor your blood pressure and heart rate regularly at home, if advised by your doctor.
  • Avoid or limit alcohol consumption, as it can increase the effects of propranolol.
  • Be aware that propranolol can mask the signs of low blood sugar (hypoglycemia), especially if you have diabetes.
  • Avoid activities requiring mental alertness, such as driving or operating machinery, until you know how this medication affects you, as it can cause dizziness or drowsiness.
  • Inform your doctor or dentist that you are taking propranolol before any surgery or dental procedures.

Dosing & Administration

đŸ‘¨â€âš•ī¸

Adult Dosing

Standard Dose: Varies by indication. For hypertension: 40 mg twice daily initially. For angina: 80-320 mg/day in 2-4 divided doses. For migraine prophylaxis: 80 mg/day initially, up to 160-240 mg/day.
Dose Range: 20 - 640 mg

Condition-Specific Dosing:

Hypertension: Initial: 40 mg twice daily; Maintenance: 120-240 mg/day in 2-3 divided doses.
Angina Pectoris: Initial: 80 mg/day in 2-4 divided doses; Maintenance: 160-320 mg/day.
Arrhythmias: 10-30 mg three or four times daily.
Migraine Prophylaxis: Initial: 80 mg/day in divided doses; Maintenance: 160-240 mg/day.
Essential Tremor: Initial: 40 mg twice daily; Maintenance: 120-320 mg/day.
Hypertrophic Subaortic Stenosis: 20-40 mg three or four times daily.
Pheochromocytoma (adjunct to alpha-blocker): 60 mg/day for 3 days pre-op; 30 mg/day for non-surgical.
đŸ‘ļ

Pediatric Dosing

Neonatal: Not established for routine use; specific indications (e.g., infantile hemangioma) require specialized dosing.
Infant: Not established for routine use; specific indications (e.g., infantile hemangioma) require specialized dosing.
Child: Hypertension: 0.5-1 mg/kg/day in 2-4 divided doses, max 2 mg/kg/day or 60 mg/day. Migraine prophylaxis: 10-20 mg 2-3 times daily. Infantile Hemangioma: 0.5-1 mg/kg/day, titrated up to 2-3 mg/kg/day.
Adolescent: Dosing similar to adult for some indications, adjusted by weight.
âš•ī¸

Dose Adjustments

Renal Impairment:

Mild: No adjustment typically needed.
Moderate: No adjustment typically needed.
Severe: Use with caution; consider lower initial doses and monitor response. Accumulation of active metabolites may occur.
Dialysis: Propranolol is not significantly removed by hemodialysis. No supplemental dose needed after dialysis. Use with caution in ESRD due to potential for increased levels of active metabolites.

Hepatic Impairment:

Mild: Consider lower initial doses and monitor response.
Moderate: Significant dose reduction required (e.g., 50% or more) due to extensive hepatic metabolism. Monitor closely.
Severe: Contraindicated or use with extreme caution and significant dose reduction. Monitor for adverse effects and drug levels if possible.

Pharmacology

đŸ”Ŧ

Mechanism of Action

Propranolol is a non-selective beta-adrenergic receptor blocker. It competitively blocks beta-1 (myocardial) and beta-2 (bronchial and vascular smooth muscle) adrenergic receptors. This leads to decreased heart rate, decreased myocardial contractility, decreased cardiac output, and reduced blood pressure. It also inhibits renin release from the kidneys. Its anti-migraine effect is thought to be due to its ability to block beta-2 receptors in cerebral vasculature, preventing vasodilation, and potentially central effects.
📊

Pharmacokinetics

Absorption:

Bioavailability: 25-50% (highly variable due to extensive first-pass metabolism)
Tmax: 1-1.5 hours (immediate release); 6 hours (extended release)
FoodEffect: Food increases bioavailability and reduces peak plasma concentrations, leading to a smoother plasma profile.

Distribution:

Vd: 4 L/kg
ProteinBinding: 90-95%
CnssPenetration: Yes (lipophilic, crosses blood-brain barrier)

Elimination:

HalfLife: 3-6 hours (immediate release); 8-11 hours (extended release)
Clearance: 0.16-0.36 L/hr/kg
ExcretionRoute: Renal (primarily as metabolites)
Unchanged: <1% (in urine)
âąī¸

Pharmacodynamics

OnsetOfAction: Within 30 minutes (oral)
PeakEffect: 1-1.5 hours (oral)
DurationOfAction: 6-12 hours (immediate release); 24 hours (extended release)

Safety & Warnings

âš ī¸

BLACK BOX WARNING

WARNING: Abrupt Cessation of Therapy. Exacerbation of angina pectoris and, in some cases, myocardial infarction and ventricular arrhythmia have been observed in patients with coronary artery disease following abrupt cessation of therapy with beta-blockers. When discontinuing chronically administered propranolol, particularly in patients with ischemic heart disease, the dosage should be gradually reduced over a period of 1 to 2 weeks and the patient should be carefully monitored. If angina markedly worsens or acute coronary insufficiency develops, propranolol administration should be reinstituted promptly, at least temporarily, and other measures appropriate for the management of unstable angina pectoris should be taken. Patients should be warned against interruption or discontinuation of therapy without the physician's advice. Because coronary artery disease is common and may be unrecognized, it may be prudent to discontinue propranolol therapy slowly even in patients treated only for hypertension.
âš ī¸

Side Effects

Urgent Side Effects: Seek Medical Help Right Away

Although rare, some people may experience severe and potentially life-threatening side effects while taking this medication. If you notice any of the following symptoms, contact your doctor immediately or seek emergency medical attention:

Signs of an allergic reaction, such as:
+ Rash or hives
+ Itching or red, swollen, blistered, or peeling skin (with or without fever)
+ Wheezing or tightness in the chest or throat
+ Difficulty breathing, swallowing, or talking
+ Unusual hoarseness or swelling of the mouth, face, lips, tongue, or throat
Signs of low blood sugar, including:
+ Dizziness or lightheadedness
+ Headache or feeling sleepy
+ Weakness, shaking, or a rapid heartbeat
+ Confusion, hunger, or sweating
Signs of lupus, such as:
+ A rash on the cheeks or other body parts
+ Easy sunburning
+ Muscle or joint pain
+ Chest pain or shortness of breath
+ Swelling in the arms or legs
Severe dizziness or fainting
New or worsening chest pain
Slow or irregular heartbeat
Shortness of breath, significant weight gain, or swelling in the arms or legs
Confusion or hallucinations (seeing or hearing things that are not there)
Memory problems or loss
Depression or other mood changes
Abnormal sensations, such as burning, numbness, or tingling
Feeling cold in the arms or legs
Changes in skin color (pale, blue, gray, purple, or red)
Changes in eyesight
Unexplained bruising or bleeding
Fever, chills, or sore throat
Erectile dysfunction
Severe skin reactions, including:
+ Stevens-Johnson syndrome (SJS)
+ Toxic epidermal necrolysis (TEN)
+ Other severe skin reactions, such as red, swollen, blistered, or peeling skin; skin irritation (with or without fever); red or irritated eyes; or sores in the mouth, throat, nose, or eyes

Other Possible Side Effects

Like all medications, this drug can cause side effects. While many people may not experience any side effects or only minor ones, it's essential to discuss any concerns with your doctor. If you experience any of the following side effects, contact your doctor if they bother you or do not go away:

Dizziness, drowsiness, tiredness, or weakness
Upset stomach or vomiting
Stomach pain or cramps
Diarrhea or constipation
Sleep disturbances
Vivid or unusual dreams

Reporting Side Effects

This list is not exhaustive, and you may experience other side effects. If you have questions or concerns about side effects, contact your doctor. You can also report side effects to the FDA at 1-800-332-1088 or online at https://www.fda.gov/medwatch.
🚨

Seek Immediate Medical Attention If You Experience:

  • Severe dizziness or fainting
  • Very slow heart rate (less than 50 beats per minute)
  • Difficulty breathing, wheezing, or shortness of breath
  • Swelling of ankles or feet, sudden weight gain (signs of heart failure)
  • Unusual tiredness or weakness
  • Coldness, numbness, or pain in fingers or toes
  • Severe depression or mood changes
📋

Before Using This Medicine

Before Taking This Medication: Important Information to Share with Your Doctor

It is essential to inform your doctor about the following:

Any allergies you have, including allergies to this medication, its components, or other substances, such as foods or drugs. Be sure to describe the allergic reaction you experienced, including any symptoms that occurred.
Certain heart conditions, including:
+ Abnormal heart rhythms (heart block or sick-sinus syndrome)
+ Heart failure (a weakened heart)
+ Low blood pressure
+ Poor blood circulation to your arms or legs
+ Shock caused by heart problems
+ A slow heartbeat
* Respiratory issues, such as:
+ Asthma
+ Chronic obstructive pulmonary disease (COPD) or other breathing problems

This list is not exhaustive, and it is crucial to discuss all your medications (prescription, over-the-counter, natural products, and vitamins) and health conditions with your doctor and pharmacist. They will help determine if it is safe to take this medication with your existing treatments and health status. Never start, stop, or adjust the dosage of any medication without first consulting your doctor.
âš ī¸

Precautions & Cautions

Important Warnings and Cautions

It is essential to inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication.

Caution with Daily Activities
Until you know how this medication affects you, avoid driving and other activities that require you to be alert. To minimize the risk of dizziness or fainting, get up slowly from a sitting or lying down position, and be cautious when climbing stairs.

Monitoring and Lab Tests
Follow your doctor's instructions for monitoring your blood pressure and heart rate. Be aware that this medication may affect certain laboratory tests, so inform all your healthcare providers and lab personnel that you are taking this medication.

Interactions with Other Substances
Discuss with your doctor before consuming alcohol. If you smoke, talk to your doctor about the potential risks. This medication may mask some symptoms of low blood sugar, such as a rapid heartbeat, which can increase the risk of severe or prolonged hypoglycemia, especially in people with diabetes, children, and those who are fasting or have undergone surgery.

Diabetes Management
If you have high blood sugar (diabetes), closely monitor your blood sugar levels while taking this medication.

Stopping the Medication
Do not stop taking this medication abruptly, as this can lead to worsening chest pain and, in some cases, heart attack, especially if you have certain types of heart disease. To avoid side effects, your doctor will instruct you on how to gradually stop taking this medication. If you experience new or worsening chest pain or other heart problems, contact your doctor immediately.

Thyroid Conditions
This medication may make it more challenging to recognize symptoms of an overactive thyroid, such as a rapid heartbeat. If you have an overactive thyroid and stop taking this medication suddenly, your condition may worsen and become life-threatening. Consult with your doctor if you have any concerns.

Interactions with Other Medications
If you have high blood pressure, talk to your doctor before taking over-the-counter (OTC) products that may increase blood pressure, such as cough or cold medications, diet pills, stimulants, non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen or naproxen, and certain natural products or aids.

Allergic Reactions
If you have a history of severe allergic reactions, discuss with your doctor the potential risks of anaphylaxis. If you use epinephrine to treat severe allergic reactions, inform your doctor, as this medication may affect the efficacy of epinephrine.

Pregnancy and Breastfeeding
If you are pregnant, plan to become pregnant, or are breastfeeding, consult with your doctor to discuss the benefits and risks of taking this medication to you and your baby.
🆘

Overdose Information

Overdose Symptoms:

  • Severe bradycardia (very slow heart rate)
  • Severe hypotension (very low blood pressure)
  • Cardiogenic shock
  • Heart failure
  • Bronchospasm (difficulty breathing)
  • Hypoglycemia (low blood sugar)
  • Seizures
  • Coma

What to Do:

Seek immediate medical attention. Call 911 or your local emergency number. For poison control, call 1-800-222-1222. Treatment may involve atropine for bradycardia, glucagon, intravenous fluids, vasopressors, and bronchodilators.

Drug Interactions

đŸšĢ

Contraindicated Interactions

  • Non-dihydropyridine calcium channel blockers (e.g., verapamil, diltiazem) - risk of severe bradycardia, heart block, heart failure.
  • MAO inhibitors - risk of severe hypertension (theoretical, due to potential for increased catecholamines).
🔴

Major Interactions

  • Other beta-blockers (additive effects, severe bradycardia/hypotension)
  • Antiarrhythmics (e.g., amiodarone, disopyramide, flecainide, quinidine) - increased risk of bradycardia, AV block, myocardial depression.
  • Clonidine (risk of rebound hypertension upon clonidine withdrawal if propranolol is not tapered first).
  • Digoxin (increased risk of bradycardia, AV block).
  • Insulin and oral hypoglycemics (propranolol can mask symptoms of hypoglycemia and prolong hypoglycemic episodes).
  • Alpha-1 blockers (e.g., prazosin, doxazosin) - increased risk of first-dose hypotension.
  • Phenothiazines (e.g., chlorpromazine, thioridazine) - increased plasma levels of both drugs.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine, quinidine) - increased propranolol levels.
  • CYP1A2 inhibitors (e.g., fluvoxamine, cimetidine) - increased propranolol levels.
🟡

Moderate Interactions

  • NSAIDs (e.g., ibuprofen, naproxen) - may reduce antihypertensive effect of propranolol.
  • Sympathomimetics (e.g., epinephrine, pseudoephedrine) - reduced beta-agonist effect, potential for unopposed alpha-stimulation (hypertension, bradycardia).
  • Ergot alkaloids (e.g., ergotamine) - increased risk of peripheral ischemia.
  • Rifampin, phenobarbital, phenytoin (CYP inducers) - decreased propranolol levels.
  • Alcohol (may increase propranolol levels and enhance hypotensive effect).
đŸŸĸ

Minor Interactions

  • Antacids (aluminum/magnesium hydroxide) - may decrease propranolol absorption (separate administration).
  • Cholestyramine/colestipol - may decrease propranolol absorption.

Monitoring

đŸ”Ŧ

Baseline Monitoring

Blood Pressure (BP)

Rationale: To establish baseline and guide initial dosing for hypertension or other cardiovascular conditions.

Timing: Prior to initiation of therapy.

Heart Rate (HR)

Rationale: To establish baseline and assess for bradycardia, a common side effect.

Timing: Prior to initiation of therapy.

Electrocardiogram (ECG)

Rationale: To assess for pre-existing conduction abnormalities (e.g., AV block) or arrhythmias.

Timing: Prior to initiation, especially in patients with cardiac history.

Renal Function (BUN, Creatinine)

Rationale: Although primarily metabolized by liver, severe renal impairment can affect metabolite excretion.

Timing: Prior to initiation, especially in patients with renal disease.

Liver Function Tests (LFTs)

Rationale: Propranolol is extensively metabolized by the liver; hepatic impairment requires dose adjustment.

Timing: Prior to initiation, especially in patients with hepatic disease.

Blood Glucose

Rationale: Propranolol can mask symptoms of hypoglycemia and prolong hypoglycemic episodes, especially in diabetics.

Timing: Prior to initiation, especially in diabetic patients.

📊

Routine Monitoring

Blood Pressure (BP)

Frequency: Regularly (e.g., weekly initially, then monthly or as clinically indicated)

Target: Individualized based on indication (e.g., <130/80 mmHg for hypertension)

Action Threshold: Hypotension (e.g., SBP <90 mmHg or symptomatic), uncontrolled hypertension.

Heart Rate (HR)

Frequency: Regularly (e.g., weekly initially, then monthly or as clinically indicated)

Target: Typically >50-60 bpm (unless specific therapeutic goal for lower HR)

Action Threshold: Bradycardia (<50 bpm or symptomatic), significant changes from baseline.

Symptoms of Bronchospasm/Dyspnea

Frequency: At each visit

Target: N/A

Action Threshold: New or worsening shortness of breath, wheezing, especially in patients with asthma/COPD.

Symptoms of Heart Failure

Frequency: At each visit

Target: N/A

Action Threshold: New or worsening edema, weight gain, dyspnea, fatigue.

Blood Glucose (in diabetics)

Frequency: Regularly, as per diabetes management plan

Target: Individualized

Action Threshold: Frequent or severe hypoglycemic episodes.

đŸ‘ī¸

Symptom Monitoring

  • Bradycardia (slow pulse)
  • Hypotension (dizziness, lightheadedness, fainting)
  • Fatigue, weakness
  • Shortness of breath, wheezing, cough (especially in patients with underlying respiratory disease)
  • Cold extremities (fingers and toes)
  • Insomnia, nightmares
  • Depression
  • Nausea, vomiting, diarrhea, constipation
  • Sexual dysfunction

Special Patient Groups

🤰

Pregnancy

Propranolol is Pregnancy Category C. It should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Beta-blockers can cause fetal growth restriction, bradycardia, and hypoglycemia in the neonate. Neonates exposed to beta-blockers in utero should be monitored for signs of bradycardia, hypoglycemia, and respiratory depression for the first few days of life.

Trimester-Specific Risks:

First Trimester: Limited data, but generally considered low risk for major malformations. Use only if clearly needed.
Second Trimester: Potential for fetal growth restriction, bradycardia, and hypoglycemia. Close fetal monitoring recommended.
Third Trimester: Increased risk of neonatal bradycardia, hypoglycemia, respiratory depression, and hypotonia. Delivery should be planned in a facility with neonatal resuscitation capabilities.
🤱

Lactation

Propranolol is excreted into breast milk in small amounts. The American Academy of Pediatrics considers it 'compatible with breastfeeding'. However, monitor breastfed infants for signs of beta-blockade (e.g., bradycardia, lethargy, poor feeding, hypoglycemia), especially in neonates or premature infants.

Infant Risk: Low to moderate risk. Monitor for bradycardia, hypotension, and hypoglycemia.
đŸ‘ļ

Pediatric Use

Dosing is weight-based and varies significantly by indication. Not recommended for routine use in very young infants except for specific conditions like infantile hemangioma. Close monitoring for adverse effects (e.g., bradycardia, hypotension, hypoglycemia) is crucial, especially in younger children.

👴

Geriatric Use

Elderly patients may be more sensitive to the effects of propranolol, particularly bradycardia and hypotension. Lower initial doses and slower titration may be necessary. Renal and hepatic function should be assessed, as age-related decline in these functions can affect drug clearance.

Clinical Information

💎

Clinical Pearls

  • Always taper propranolol gradually over 1-2 weeks when discontinuing, especially in patients with ischemic heart disease, to avoid rebound angina, MI, or arrhythmias.
  • Propranolol is non-selective, meaning it blocks both beta-1 and beta-2 receptors. This can lead to bronchospasm in patients with asthma or COPD and can mask symptoms of hypoglycemia in diabetics.
  • Food increases the bioavailability of propranolol and can reduce peak plasma concentrations, leading to a smoother effect. Consistent administration with or without food is important.
  • Patients should be advised to check their pulse regularly and report any significant slowing or symptoms of bradycardia.
  • Due to its lipophilicity, propranolol can cross the blood-brain barrier, which may contribute to CNS side effects like fatigue, insomnia, and nightmares.
  • Propranolol is often used off-label for performance anxiety (stage fright) due to its ability to reduce physical symptoms like palpitations and tremor.
🔄

Alternative Therapies

  • Other beta-blockers (e.g., metoprolol, atenolol, carvedilol, bisoprolol)
  • Calcium channel blockers (e.g., amlodipine, nifedipine, verapamil, diltiazem)
  • ACE inhibitors (e.g., lisinopril, enalapril)
  • Angiotensin Receptor Blockers (ARBs) (e.g., losartan, valsartan)
  • Diuretics (e.g., hydrochlorothiazide, furosemide)
  • Alpha-blockers (e.g., prazosin, doxazosin)
  • Other antiarrhythmics (e.g., amiodarone, sotalol)
  • Other migraine prophylactic agents (e.g., topiramate, amitriptyline, CGRP inhibitors)
💰

Cost & Coverage

Average Cost: $10 - $50 per 30 tablets (40mg)
Generic Available: Yes
Insurance Coverage: Tier 1 (Generic) or Tier 2 (Preferred Brand)
📚

General Drug Facts

If your symptoms or health issues persist or worsen, it's essential to contact your doctor for further guidance. To ensure your safety, never share your medication with others or take someone else's medication. Some medications may come with an additional patient information leaflet, so be sure to check with your pharmacist for more information. If you have any questions or concerns about your medication, don't hesitate to reach out to your doctor, nurse, pharmacist, or other healthcare provider. In the event of a suspected overdose, immediately call your local poison control center or seek emergency medical attention. When seeking help, be prepared to provide details about the medication taken, the amount, and the time it occurred.