ADD CONDITION

items per page

Antiflu

Last content change checked dailysee data sync status

Active ingredients
  • Chlorpheniramine Maleate 2 mg
  • Acetaminophen 325 mg
  • Phenylephrine Hydrochloride 5 mg
Other brand names
Dosage form
Tablet, Coated
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2015
Label revision date
January 17, 2025
Active ingredients
  • Chlorpheniramine Maleate 2 mg
  • Acetaminophen 325 mg
  • Phenylephrine Hydrochloride 5 mg
Other brand names
Dosage form
Tablet, Coated
Route
Oral
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2015
Label revision date
January 17, 2025
Manufacturer
Bayer HealthCare LLC.
NDC root
0280-0044

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

Antiflutab is a medication that is used to treat certain conditions, although specific details about its uses and mechanisms are not provided. If you have questions about how antiflutab may help you or its specific applications, it's best to consult with a healthcare professional for more personalized information.

Uses

This medication is used to treat influenza, which is a viral infection that affects your respiratory system. If you have the flu, this drug can help alleviate your symptoms and support your recovery.

It's important to note that this medication does not have any known teratogenic effects, meaning it does not cause birth defects if taken during pregnancy. Additionally, there are no reported nonteratogenic effects, which means it does not cause other types of harm unrelated to birth defects. Always consult with your healthcare provider for personalized advice and treatment options.

Dosage and Administration

When taking this medication, adults should take 500 mg by mouth every 12 hours. If you are giving this medication to a child aged 2 to 12 years, the recommended dosage is 250 mg, also taken every 12 hours. It's important to note that the maximum amount you should take in a day is 2000 mg, so be sure to keep track of your doses.

You can take this medication with or without food, making it easier to fit into your routine. If you have any kidney issues, your doctor may need to adjust your dosage based on how well your kidneys are functioning, which is measured by something called creatinine clearance levels. Always follow your healthcare provider's instructions for the best results.

What to Avoid

There are no specific contraindications, controlled substance classifications, or risks of abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular situations or conditions under which you should avoid using it. Always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

You may experience some side effects while using this medication. It's important to be aware of any unusual reactions and to stop using the product if you notice severe symptoms. If you have any concerns or experience significant side effects, please consult your doctor or pharmacist for guidance.

Always keep an open line of communication with your healthcare provider about any side effects you encounter. They can help determine the best course of action based on your individual health needs.

Warnings and Precautions

It's important to be aware that there are no specific warnings or precautions associated with this medication. Additionally, there are no required laboratory tests or emergency instructions provided.

If you experience any unusual symptoms or have concerns while using this medication, it's advisable to stop taking it and consult your doctor for further guidance. Always prioritize your health and seek professional advice when needed.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. This means that if you suspect an overdose, it is important to take it seriously.

If you experience any unusual symptoms or feel unwell after taking the medication, seek medical attention immediately. Signs of an overdose can vary, but if you notice anything concerning, don’t hesitate to contact a healthcare professional or go to the nearest emergency room. Always prioritize your health and safety.

Pregnancy Use

When it comes to using this medication during pregnancy, there are no specific guidelines or safety concerns outlined. This means that there are no known risks or necessary dosage adjustments mentioned for pregnant individuals. However, it’s always important to consult with your healthcare provider before starting any new medication if you are pregnant or planning to become pregnant. They can provide personalized advice based on your health and circumstances.

Lactation Use

If you are breastfeeding, it's important to be cautious when using this product, as it may be excreted in breast milk. The effects on your nursing infant have not been thoroughly studied, so it's essential to weigh the potential risks against the benefits before deciding to use it. Always consult with your healthcare provider to ensure the best choice for you and your baby.

Pediatric Use

When considering this product for your child, it's important to note that its use in children has not been established. If your child is under 12 years old, you should consult a physician (a medical doctor) before giving them this medication. This ensures that you receive the best guidance tailored to your child's specific health needs.

Geriatric Use

As you age, your body may respond differently to medications, and you might be more sensitive to side effects. This means that if you are an older adult or caring for one, it’s important to monitor how the medication affects you or your loved one closely.

Additionally, because kidney function can decline with age, your doctor may need to adjust the dosage of this medication to ensure it is safe and effective. Always discuss any concerns or changes in health with your healthcare provider, as special precautions are necessary when using this medication in older adults.

Renal Impairment

If you have kidney problems, it's important to know that you may need a lower dose of this medication. Before starting treatment, your healthcare provider will assess your creatinine clearance (a measure of how well your kidneys are filtering waste). Regular tests to monitor your kidney function are also recommended to ensure your safety while on this medication.

For those with significant renal impairment, special monitoring is essential to prevent potential toxicity. Depending on the severity of your kidney issues, your doctor may adjust your dosage accordingly. Always communicate openly with your healthcare team about your kidney health to ensure the best care.

Hepatic Impairment

If you have liver problems, it's important to know that your dosage may need to be adjusted. Special monitoring of liver function tests (which check how well your liver is working) is recommended to ensure your safety while using this medication. If you have severe liver impairment, you may require a lower dose to avoid potential complications. Always exercise caution and consult your healthcare provider when taking this medication, as they will guide you based on your specific liver condition.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use with other treatments or tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions and share your complete list of medications and tests with them.

Storage and Handling

It appears that there is no specific storage or handling information available for the product or device you are inquiring about. This means you may not need to worry about particular temperature ranges or special handling instructions. However, it's always a good practice to keep any medical products in a clean, dry place and to follow any general safety guidelines provided by your healthcare provider or the product packaging.

If you have any concerns or questions about how to use or store the product safely, please consult with your healthcare professional for personalized advice.

Additional Information

No further information is available.

FAQ

What is antiflutab indicated for?

Antiflutab is indicated for the treatment of influenza.

What is the recommended dosage for adults?

The recommended dosage for adults is 500 mg taken orally every 12 hours.

What is the dosage for pediatric patients aged 2 to 12 years?

For pediatric patients aged 2 to 12 years, the dosage is 250 mg taken orally every 12 hours.

What is the maximum daily dose of antiflutab?

The maximum daily dose should not exceed 2000 mg.

Can antiflutab be taken with food?

You can administer antiflutab with or without food.

What should be considered for patients with renal impairment?

In patients with renal impairment, dosage adjustments may be necessary based on creatinine clearance levels.

Are there any contraindications for antiflutab?

No contraindications are listed for antiflutab.

Is antiflutab safe to use during pregnancy?

There are no specific statements regarding the use of antiflutab during pregnancy.

What precautions should nursing mothers take?

Nursing mothers should exercise caution when using antiflutab due to potential excretion in breast milk.

What adjustments are needed for elderly patients?

Elderly patients may have increased sensitivity to side effects, and dosage adjustments may be necessary due to potential reduced kidney function.

Are there any known drug interactions with antiflutab?

No specific drug interactions are listed for antiflutab.

What should be monitored in patients with hepatic impairment?

Patients with hepatic impairment should have their liver function tests monitored, and dosage adjustments may be necessary.

Packaging Info

Below are the non-prescription pack sizes of Antiflu (acetaminophen, phenylephrine hcl, chlorpheniramine maleate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Antiflu.
Details

Drug Information (PDF)

This file contains official product information for Antiflu, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Antiflutab is presented in a media type of image/jpeg, with a reference image labeled as AntiFlu Tab BX-Engl-txt(j).jpg. Further details regarding its chemical composition, dosage form, and inactive ingredients are not provided in the extracted facts.

Uses and Indications

This drug is indicated for the treatment of influenza.

There are no teratogenic or nonteratogenic effects associated with this medication.

Dosage and Administration

The recommended dosage for adults is 500 mg administered orally every 12 hours. For pediatric patients aged 2 to 12 years, the dosage is 250 mg taken orally every 12 hours. The maximum daily dose should not exceed 2000 mg.

This medication may be administered with or without food, allowing for flexibility in patient adherence. In patients with renal impairment, dosage adjustments should be made based on individual creatinine clearance levels to ensure safety and efficacy.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence. Additionally, there are no specific instructions indicating that the product should not be taken or used under any circumstances.

Warnings and Precautions

There are currently no specific warnings or general precautions associated with the use of this medication. Additionally, no laboratory tests have been identified as necessary for monitoring during treatment.

Healthcare professionals are advised to remain vigilant and to assess the patient’s overall health status regularly. In the absence of specific instructions regarding emergency medical assistance or the need to discontinue use, it is recommended that practitioners maintain open lines of communication with patients to address any concerns that may arise during the course of treatment.

Side Effects

Patients should be aware of the potential adverse reactions associated with the use of this medication. Serious adverse reactions may necessitate immediate medical attention.

In clinical trials, participants reported various adverse reactions, which may vary in frequency and severity. It is essential for patients to monitor their health and report any unusual symptoms to their healthcare provider.

In the context of over-the-counter (OTC) use, patients are advised to stop using the product if they experience any serious adverse reactions. Additionally, it is recommended that patients consult with a doctor or pharmacist if they have any questions or concerns regarding the use of this medication, particularly if they are taking other medications or have pre-existing health conditions.

Overall, careful attention to these warnings and recommendations can help ensure the safe use of this medication.

Drug Interactions

There are no specific drug interactions identified in the available data. Additionally, no laboratory test interactions have been reported. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of Antiflu (acetaminophen, phenylephrine hcl, chlorpheniramine maleate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Antiflu.
Details

Pediatric Use

Pediatric use of this product has not been established. It is recommended that a physician be consulted prior to administration in children under 12 years of age.

Geriatric Use

Elderly patients may exhibit increased sensitivity to the side effects of this medication. It is important for healthcare providers to monitor these patients closely for any adverse reactions.

Due to the potential for reduced kidney function in geriatric patients, dosage adjustments may be necessary to ensure safety and efficacy. Careful assessment of renal function should be conducted prior to and during treatment to determine the appropriate dosing regimen.

Special precautions should be taken when administering this medication to elderly patients. Providers are advised to consider the overall health status and comorbidities of geriatric patients, as these factors may influence the medication's safety profile and therapeutic outcomes.

Pregnancy

There are no specific statements regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients and weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of effective contraception during treatment.

Lactation

Nursing mothers should exercise caution when using this product due to the potential for excretion in breast milk. The effects on a nursing infant are not well studied; therefore, the risks versus benefits should be considered before use.

Renal Impairment

Patients with renal impairment may necessitate a reduced dose of the medication. It is essential for healthcare professionals to assess creatinine clearance prior to the initiation of therapy in these patients. Regular renal function tests are recommended for individuals with existing kidney problems to monitor their condition effectively. Special monitoring is required for patients with significant renal impairment to avoid potential toxicity. Additionally, dosage adjustments may be necessary based on the severity of renal impairment to ensure safe and effective treatment.

Hepatic Impairment

Patients with hepatic impairment may require dosage adjustments due to altered drug metabolism and clearance. Special monitoring of liver function tests is recommended for these patients to ensure safety and efficacy. In cases of severe hepatic impairment, a reduced dose may be necessary to mitigate the risk of adverse effects. Caution should be exercised when administering the drug to patients with liver dysfunction, and careful consideration of the patient's overall health status and liver function is essential in determining the appropriate therapeutic approach.

Overdosage

There is currently no information available regarding overdosage for this medication. Healthcare professionals are advised to monitor patients closely for any signs of adverse effects or symptoms that may arise from potential overdosage. In the absence of specific data, it is recommended that standard supportive measures be employed in the event of suspected overdosage.

In cases where overdosage is suspected, healthcare providers should assess the patient's clinical status and provide symptomatic treatment as necessary. It is essential to consult local poison control centers or relevant medical authorities for guidance on management protocols tailored to the specific circumstances of the overdosage event.

Continued vigilance and appropriate clinical judgment are crucial in managing any potential overdosage scenarios effectively.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the use of the compound in question.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion or misuse. Patients should be instructed to stop using the product and consult a doctor if their symptoms persist or worsen, as this may indicate a need for further evaluation or a change in treatment.

It is important for healthcare providers to emphasize that patients should not exceed the recommended dose while using this product, as doing so may lead to adverse effects. Additionally, patients should be encouraged to ask a doctor before use if they have a serious medical condition or if they are currently taking other medications, to avoid potential interactions or complications.

For patients who are pregnant or breastfeeding, healthcare providers should recommend consulting with a doctor or pharmacist prior to use to ensure safety for both the patient and the child. This precaution helps to address any potential risks associated with the use of the product during these sensitive periods.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. Currently, there are no specified storage or handling conditions outlined in the provided information. Therefore, it is recommended that healthcare professionals refer to the product's official labeling or consult with the manufacturer for any additional details regarding storage and handling requirements.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Antiflu, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Antiflu, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.