Alahist IR 2mg Tablets

Manufacturer POLY Active Ingredient Dexbrompheniramine Tablets(DEX brome fen IR a meen) Pronunciation DEX-brohm-FEN-ir-a-meen
It is used to ease allergy signs.
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Drug Class
Antihistamine
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Pharmacologic Class
H1-receptor antagonist (first-generation)
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Pregnancy Category
Category C
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FDA Approved
Jan 1970
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DEA Schedule
Not Controlled

Overview

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What is this medicine?

Alahist IR contains dexbrompheniramine, an antihistamine that helps relieve allergy symptoms like sneezing, runny nose, and itchy eyes. It works by blocking a natural substance called histamine that your body makes during an allergic reaction. This medication can make you feel drowsy.
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How to Use This Medicine

Taking Your Medication

To use this medication correctly, follow your doctor's instructions and read all the information provided. You can take this medication with or without food. If it causes stomach upset, taking it with food may help.

Storing and Disposing of Your Medication

Keep your medication at room temperature in a dry place, avoiding storage in a bathroom. Ensure all medications are stored safely and out of reach of children and pets. When disposing of unused or expired medication, do not flush it down the toilet or pour it down the drain unless instructed to do so. Instead, consult your pharmacist for guidance on proper disposal. Many communities have drug take-back programs, which your pharmacist can help you find.

Missing a Dose

If you take this medication regularly and miss a dose, take it as soon as you remember. However, if it's close to the time for your next dose, skip the missed dose and resume your regular schedule. Do not take two doses at once or extra doses. If you take this medication as needed, follow your doctor's instructions and do not take it more frequently than recommended.
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Lifestyle & Tips

  • Avoid driving or operating heavy machinery until you know how this medication affects you, as it can cause drowsiness or dizziness.
  • Avoid alcohol and other medications that cause drowsiness, as this can worsen the sedative effects.
  • Drink plenty of fluids to help with dry mouth, a common side effect.
  • If you experience blurred vision, avoid activities requiring clear vision.
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Available Forms & Alternatives

Dosing & Administration

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Adult Dosing

Standard Dose: 2 mg orally every 4 to 6 hours
Dose Range: 2 - 12 mg

Condition-Specific Dosing:

maximumDailyDose: 12 mg
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Pediatric Dosing

Neonatal: Not established
Infant: Not established (generally not recommended for children under 2 years)
Child: 6-12 years: 1 mg orally every 4 to 6 hours (maximum 6 mg/day)
Adolescent: >12 years: 2 mg orally every 4 to 6 hours (maximum 12 mg/day)
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Dose Adjustments

Renal Impairment:

Mild: Use with caution; consider lower starting dose
Moderate: Use with caution; consider dose reduction
Severe: Use with caution; significant dose reduction or avoidance may be necessary due to increased risk of adverse effects
Dialysis: Considerations: Not well studied; likely not dialyzable due to high protein binding and large volume of distribution. Avoid or use with extreme caution.

Hepatic Impairment:

Mild: Use with caution; consider lower starting dose
Moderate: Use with caution; consider dose reduction
Severe: Use with caution; significant dose reduction or avoidance may be necessary due to impaired metabolism and increased risk of adverse effects

Pharmacology

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Mechanism of Action

Dexbrompheniramine is a first-generation antihistamine that competitively antagonizes H1-histamine receptors, thereby preventing histamine from binding and producing its effects (e.g., vasodilation, increased capillary permeability, pruritus, bronchoconstriction). It also possesses significant anticholinergic (drying) and sedative properties due to its ability to cross the blood-brain barrier and block muscarinic acetylcholine receptors.
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Pharmacokinetics

Absorption:

Bioavailability: Not precisely quantified, but well absorbed orally
Tmax: Approximately 2-5 hours
FoodEffect: Food may slightly delay absorption but does not significantly affect the extent of absorption.

Distribution:

Vd: Not precisely quantified, but widely distributed throughout body tissues
ProteinBinding: Approximately 70-80%
CnssPenetration: Yes

Elimination:

HalfLife: Approximately 10-25 hours (highly variable)
Clearance: Not precisely quantified
ExcretionRoute: Primarily renal (urine), with some fecal excretion
Unchanged: Small percentage (less than 1%)
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Pharmacodynamics

OnsetOfAction: Within 15-60 minutes
PeakEffect: Approximately 2-6 hours
DurationOfAction: 4-6 hours

Safety & Warnings

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Side Effects

Urgent Side Effects: Seek Medical Help Immediately
If you experience any of the following symptoms, call your doctor or seek medical attention right away, as they may be signs of a severe and potentially life-threatening reaction:
- Signs of an allergic reaction, such as rash, hives, itching, red, swollen, blistered, or peeling skin (with or without fever), wheezing, tightness in the chest or throat, trouble breathing, swallowing, or talking, unusual hoarseness, or swelling of the mouth, face, lips, tongue, or throat.

Other Possible Side Effects
Most medications can cause side effects, but many people either do not experience them or have only mild symptoms. If you encounter any of the following side effects or any other unusual effects that bother you or do not go away, contact your doctor for advice:
- Feeling sleepy
- Feeling nervous and excitable

Note: This list does not include all possible side effects. If you have concerns about side effects, consult your doctor. For medical advice regarding 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.
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Seek Immediate Medical Attention If You Experience:

  • Severe drowsiness or sedation that interferes with daily activities
  • Significant dizziness or lightheadedness
  • Difficulty urinating or painful urination
  • Severe dry mouth or throat
  • Blurred vision or changes in vision
  • Confusion, hallucinations, or unusual excitement (especially in children or elderly)
  • Fast or irregular heartbeat
  • Signs of an allergic reaction (rash, itching/swelling, severe dizziness, trouble breathing)
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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 symptoms you experienced as a result of the allergy.
All medications you are currently taking, including prescription and over-the-counter (OTC) drugs, natural products, and vitamins. This information will help your doctor and pharmacist assess potential interactions between this medication and other substances you are taking.
* Any existing health problems, as this medication may interact with certain conditions.

To ensure your safety, it is crucial to verify that it is safe to take this medication with all your current medications and health conditions. Never start, stop, or adjust the dose of any medication without first consulting your doctor.
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Precautions & Cautions

It is essential to inform all your healthcare providers, including doctors, nurses, pharmacists, and dentists, that you are taking this medication. To minimize the risk of severe side effects, do not exceed the dosage prescribed by your doctor. Adhering to the recommended treatment duration is also crucial; do not take this drug for longer than specified by your healthcare provider.

Until you are familiar with how this medication affects you, it is advisable to avoid operating a vehicle, performing tasks that require alertness, or engaging in activities that demand your full attention. Additionally, refrain from consuming alcohol while taking this drug, as it may exacerbate its effects.

Before using marijuana, other cannabis products, or any prescription or over-the-counter (OTC) medications that may cause drowsiness or impair your reactions, consult with your doctor to discuss potential interactions. If the patient is a child, exercise caution when administering this drug, as children may be at a higher risk of experiencing excitability.

If you are pregnant, planning to become pregnant, or are breast-feeding, it is crucial to discuss the benefits and risks of this medication with your doctor, considering both your health and the well-being of your baby.
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Overdose Information

Overdose Symptoms:

  • Severe drowsiness or deep sleep (coma)
  • Severe dry mouth, nose, and throat
  • Flushing of the skin
  • Dilated pupils
  • Blurred vision
  • Fever
  • Agitation, hallucinations, seizures (especially in children)
  • Loss of coordination
  • Rapid or irregular heartbeat
  • Low blood pressure
  • Urinary retention

What to Do:

In case of suspected overdose, seek immediate medical attention or call a poison control center. In the US, call 1-800-222-1222. Be prepared to provide information about the medication taken, dose, and time.

Drug Interactions

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Contraindicated Interactions

  • Monoamine Oxidase Inhibitors (MAOIs) (concurrent use or within 14 days of MAOI discontinuation)
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Major Interactions

  • Alcohol
  • Other CNS depressants (e.g., opioids, benzodiazepines, sedatives, hypnotics, anxiolytics, tricyclic antidepressants)
  • Other anticholinergic drugs (e.g., atropine, scopolamine, some antipsychotics, some antidepressants, other antihistamines)
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Moderate Interactions

  • Potassium chloride (oral forms) (increased risk of GI lesions due to anticholinergic effects)
  • Beta-2 agonists (e.g., albuterol) (potential for additive cardiovascular effects, though less common)
  • Metoclopramide (antagonism of prokinetic effect)
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Minor Interactions

  • Not specifically identified for minor interactions; generally additive effects with other drugs causing similar side effects.

Monitoring

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Baseline Monitoring

Patient history (allergies, pre-existing conditions like glaucoma, prostatic hypertrophy, asthma, cardiovascular disease)

Rationale: To identify contraindications or conditions requiring caution due to anticholinergic or sedative effects.

Timing: Prior to initiation of therapy

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Routine Monitoring

Symptom relief (e.g., sneezing, rhinorrhea, itching)

Frequency: As needed, during therapy

Target: Reduction or resolution of target symptoms

Action Threshold: Lack of efficacy may indicate need for alternative therapy or dose adjustment.

Adverse effects (e.g., drowsiness, dizziness, dry mouth, blurred vision, urinary retention, constipation)

Frequency: Regularly, especially during initial therapy and dose adjustments

Target: Absence or mild, tolerable side effects

Action Threshold: Severe or intolerable side effects warrant dose reduction or discontinuation.

Mental status/Cognitive function (especially in elderly or children)

Frequency: Periodically, as clinically indicated

Target: Normal cognitive function for age

Action Threshold: Signs of confusion, disorientation, or paradoxical excitation require immediate evaluation and discontinuation.

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Symptom Monitoring

  • Drowsiness
  • Dizziness
  • Dry mouth
  • Blurred vision
  • Urinary retention
  • Constipation
  • Nervousness
  • Insomnia (paradoxical effect, especially in children)
  • Tachycardia
  • Hypotension

Special Patient Groups

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Pregnancy

Category C. Use during pregnancy only if the potential benefit justifies the potential risk to the fetus. Studies in animals have shown adverse effects, and there are no adequate and well-controlled studies in pregnant humans. First-generation antihistamines are generally avoided in the third trimester due to potential for adverse effects in the neonate.

Trimester-Specific Risks:

First Trimester: Limited data; generally considered low risk for major malformations, but caution advised.
Second Trimester: Generally considered safer than first or third trimester, but still use with caution.
Third Trimester: Potential for adverse effects in the neonate, including irritability, tremors, and respiratory distress, due to anticholinergic effects. Avoid use if possible.
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Lactation

Not recommended. Dexbrompheniramine is excreted into breast milk and can cause drowsiness, irritability, or paradoxical excitation in the nursing infant. It may also decrease milk supply due to its anticholinergic effects. If use is unavoidable, monitor infant closely for adverse effects.

Infant Risk: Moderate to High (L3-L4) - Risk of sedation, irritability, and potential for decreased milk supply.
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Pediatric Use

Use with caution, especially in children under 6 years of age. Not recommended for children under 2 years due to increased risk of respiratory depression and paradoxical excitation. Children may be more susceptible to the sedative and anticholinergic effects, or may experience paradoxical excitation (nervousness, restlessness, insomnia).

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Geriatric Use

Use with extreme caution. Elderly patients are more susceptible to the sedative, anticholinergic (e.g., dry mouth, blurred vision, urinary retention, constipation), and hypotensive effects. Increased risk of falls, confusion, and delirium. Lower doses are often recommended, and alternative non-sedating antihistamines should be considered.

Clinical Information

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Clinical Pearls

  • Dexbrompheniramine is a first-generation antihistamine known for its significant sedative and anticholinergic side effects.
  • Patients should be warned about impaired ability to drive or operate machinery.
  • Avoid concurrent use with alcohol or other CNS depressants.
  • Exercise caution in elderly patients due to increased susceptibility to adverse effects, particularly confusion, urinary retention, and falls.
  • Not recommended for children under 2 years of age; use with caution in older children due to risk of paradoxical excitation.
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Alternative Therapies

  • Second-generation antihistamines (e.g., Loratadine, Cetirizine, Fexofenadine, Levocetirizine, Desloratadine) - generally preferred due to less sedation and anticholinergic effects.
  • Nasal corticosteroids (e.g., Fluticasone, Mometasone) - for allergic rhinitis.
  • Mast cell stabilizers (e.g., Cromolyn sodium) - for allergy prevention.
  • Decongestants (e.g., Pseudoephedrine, Phenylephrine) - often combined with antihistamines for congestion relief.
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Cost & Coverage

Average Cost: $5 - $20 per 30 tablets (generic 2mg)
Generic Available: Yes
Insurance Coverage: Tier 1 (Preferred Generic)
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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 medical attention. When seeking help, be prepared to provide details about the medication taken, the amount, and the time it happened.