Brompheniramine: Difference between revisions

Brompheniramine
	Adult Indications & Dosage
	Pediatric Indications & Dosage
	Contraindications
	Warnings & Precautions
	Adverse Reactions
	Drug Interactions
	Use in Specific Populations
	Administration & Monitoring
	Overdosage
	Pharmacology
	Clinical Studies
	How Supplied
	Images
	Patient Counseling Information
	Precautions with Alcohol
	Brand Names
	Look-Alike Names

VisualWikitext

Latest revision as of 18:19, 18 August 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

Disclaimer

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NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Overview

Brompheniramine is an anticholinergic that is FDA approved for the treatment of hay fever (allergic rhinitis) or upper respiratory allergies. Common adverse reactions include hypersensitivity, drowsiness.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Temporarily relieves these symptoms due to hay fever (allergic rhinitis) or upper respiratory allergies:

Runny nose.
Sneezing.
Itching of the nose or throat.
Itchy, watery eyes.

Off-Label Use and Dosage (Adult)

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Brompheniramine in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

There is limited information regarding FDA-Labeled Use of Brompheniramine in pediatric patients.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Brompheniramine in pediatric patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Brompheniramine in pediatric patients.

Contraindications

Hypersensitivity to any of the ingredients.

Warnings

Ask a doctor before use if you have

A breathing problem such as emphysema or chronic bronchitis.
Glaucoma.
Trouble urinating due to enlargement of the prostate gland.

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
When using this product.

Excitability may occur, especially in children.
May cause drowsiness.
Avoid alcoholic drinks.
Alcohol, sedatives, and tranquilizers may increase the drowsiness effect.
Use caution when driving a motor vehicle or operating machinery.

If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

Overdose may cause hallucinations, convulsions, and death.

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Clinical Trial Experience of Brompheniramine in the drug label.

Postmarketing Experience

There is limited information regarding Postmarketing Experience of Brompheniramine in the drug label.

Drug Interactions

There is limited information regarding Brompheniramine Drug Interactions in the drug label.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA):

Pregnancy Category

Pregnancy Category (AUS):

Australian Drug Evaluation Committee (ADEC) Pregnancy Category

There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Brompheniramine in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Brompheniramine during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Brompheniramine with respect to nursing mothers.

Pediatric Use

There is no FDA guidance on the use of Brompheniramine with respect to pediatric patients.

Geriatic Use

There is no FDA guidance on the use of Brompheniramine with respect to geriatric patients.

Gender

There is no FDA guidance on the use of Brompheniramine with respect to specific gender populations.

Race

There is no FDA guidance on the use of Brompheniramine with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Brompheniramine in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Brompheniramine in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Brompheniramine in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Brompheniramine in patients who are immunocompromised.

Administration and Monitoring

Administration

Oral.

Monitoring

There is limited information regarding Monitoring of Brompheniramine in the drug label.

IV Compatibility

There is limited information regarding IV Compatibility of Brompheniramine in the drug label.

Overdosage

There is limited information regarding Chronic Overdose of Brompheniramine in the drug label.

Pharmacology

There is limited information regarding Brompheniramine Pharmacology in the drug label.

Mechanism of Action

There is limited information regarding Brompheniramine Mechanism of Action in the drug label.

Structure

There is limited information regarding Brompheniramine Structure in the drug label.

Pharmacodynamics

There is limited information regarding Pharmacodynamics of Brompheniramine in the drug label.

Pharmacokinetics

There is limited information regarding Pharmacokinetics of Brompheniramine in the drug label.

Nonclinical Toxicology

There is limited information regarding Nonclinical Toxicology of Brompheniramine in the drug label.

Clinical Studies

There is limited information regarding Clinical Studies of Brompheniramine in the drug label.

How Supplied

Supplied in a tight, light-resistant container with a child-resistant cap.
Contains color additives including FD&C Yellow No. 5 (tartrazine).
Ala-Hist IR Tablets are dark green caplet shaped, scored tablets, debossed "Poly" bisect "783" on one side and plain on the other

Storage

Store at 15° - 30°C (59° - 86°F).

Images

Drug Images

{{#ask: Page Name::Brompheniramine |?Pill Name |?Drug Name |?Pill Ingred |?Pill Imprint |?Pill Dosage |?Pill Color |?Pill Shape |?Pill Size (mm) |?Pill Scoring |?NDC |?Drug Author |format=template |template=DrugPageImages |mainlabel=- |sort=Pill Name }}

Package and Label Display Panel

This image is provided by the National Library of Medicine.

{{#ask: Label Page::Brompheniramine |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}

Patient Counseling Information

Directions for Use

Precautions with Alcohol

Alcohol-Brompheniramine interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

ALA-HIST IR ®^[1]

Look-Alike Drug Names

There is limited information regarding Brompheniramine Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

↑ "ALA-HIST IR- dexbrompheniramine maleate tablet".

{{#subobject:

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 |Label Name=Bromphen 01.jpg

}}

{{#subobject:

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 |Label Name=Bromiphen 02.jpg

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{{#subobject:

 |Label Page=Brompheniramine
 |Label Name=Bromphen 04.png

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[1] "ALA-HIST IR- dexbrompheniramine maleate tablet".

[1]

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+|aOrAn=an
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+:* [[Runny nose]].
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-:* Dosage
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+Hypersensitivity to any of the ingredients.
-<!--Warnings-->
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-|warnings=* Description
+:* A breathing problem such as [[emphysema]] or [[chronic bronchitis]].
+:* [[Glaucoma]].
-====Precautions====
+:* Trouble urinating due to enlargement of the [[prostate gland]].
+* Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
-* Description
+* When using this product.
+:* Excitability may occur, especially in children.
-<!--Adverse Reactions-->
+:* May cause [[drowsiness]].
+:* Avoid alcoholic drinks.
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+:* Alcohol, [[sedatives]], and [[tranquilizers]] may increase the drowsiness effect.
+:* Use caution when driving a motor vehicle or operating machinery.
+* If [[pregnant]] or [[breast]]-feeding, ask a health professional before use.
+* Keep out of reach of children.
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 |clinicalTrials=There is limited information regarding <i>Clinical Trial Experience</i> of {{PAGENAME}} in the drug label.
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-=====Metabolic and Nutritional=====
-=====Musculoskeletal=====
-=====Neurologic=====
-=====Respiratory=====
-=====Skin and Hypersensitivy Reactions=====
-=====Special Senses=====
-=====Urogenital=====
-=====Miscellaneous=====
-<!--Postmarketing Experience-->
 |postmarketing=There is limited information regarding <i>Postmarketing Experience</i> of {{PAGENAME}} in the drug label.
+|drugInteractions=<!--Use in Specific Populations-->
-=====Body as a Whole=====
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-=====Endocrine=====
-=====Hematologic and Lymphatic=====
-=====Metabolic and Nutritional=====
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@@ Line 264: / Line 74: @@
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@@ Line 313: / Line 99: @@
 <!--How Supplied-->
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+|howSupplied=* Supplied in a tight, light-resistant container with a child-resistant cap.
-|packLabel=<!--Patient Counseling Information-->
+* Contains color additives including FD&C Yellow No. 5 (tartrazine).
-|fdaPatientInfo=There is limited information regarding <i>Patient Counseling Information</i> of {{PAGENAME}} in the drug label.
+* Ala-Hist IR Tablets are dark green caplet shaped, scored tablets, debossed "Poly" bisect "783" on one side and plain on the other
+|storage=* Store at 15° - 30°C (59° - 86°F).
-<!--Precautions with Alcohol-->
+|packLabel=[[File:Bromphen 01.jpg|thumb|none|400px|This image is provided by the National Library of Medicine.]]
+[[File:Bromiphen 02.jpg|thumb|none|400px|This image is provided by the National Library of Medicine.]]
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+[[File:Bromphenramine 01.png|thumb|none|400px|This image is provided by the National Library of Medicine.]]
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Brompheniramine: Difference between revisions

Latest revision as of 18:19, 18 August 2015

Disclaimer

Overview

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Off-Label Use and Dosage (Adult)

Non–Guideline-Supported Use

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

Non–Guideline-Supported Use

Contraindications

Warnings

Adverse Reactions

Clinical Trials Experience

Postmarketing Experience

Drug Interactions

Use in Specific Populations

Pregnancy

Labor and Delivery

Nursing Mothers

Pediatric Use

Geriatic Use

Gender

Race

Renal Impairment

Hepatic Impairment

Females of Reproductive Potential and Males

Immunocompromised Patients

Administration and Monitoring

Administration

Monitoring

IV Compatibility

Overdosage

Pharmacology

Mechanism of Action

Structure

Pharmacodynamics

Pharmacokinetics

Nonclinical Toxicology

Clinical Studies

How Supplied

Storage

Images

Drug Images

Package and Label Display Panel

Patient Counseling Information

Directions for Use

Precautions with Alcohol

Brand Names

Look-Alike Drug Names

Drug Shortage Status

Price

References

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