Fexofenadine Hcl 180 Mg

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fexofenadine orally disintegrate the footsteps from the package just before keeping the pills. Place the pill on the tongue and allow it to unwind without chewing. Swallow a certain number of times while the pill is dissolving.

Fexofenadine tablets.

Drug medical testing. com. last updated on September 21, 2022.

Use of fexofenadine Pill:

  • Used to relieve allergic character.
  • Used to heal hive.

What should I tell my doctor before taking fexofenadine pills?

  • If you are allergic to to fexofenadine or other parts of this medicine. fexofenadine tablets).
  • If you are allergic to this medicine ( fexofenadine tablet); all parts of these medicines ( fexofenadine tablet); or any other kind of medicine, food, or medication. Tell your doctor about your allergy and any symptoms you have.

This medicine can interact with other medicines and health problems.

Tell your doctor and pharmacist about all your avenues (prescription or freely available medications, natural products, vitamins) and health problems. You should make sure that you are safe on the medication to ensure that it is safe for you ( fexofenadine pills) all medical medications and health problems. Do not start, stop, or change your medication dosage without consulting your doctor.

What should I do or not do while taking fexofenadine pills?

  • Tell all your own medical staff that you can do this medicine ( fexofenadine tablet) use. This applies to health care providers, nurses, pharmacists, and dentists.
  • This medication may affect certain laboratory tests. Tell all of your own health care providers and the laboratory that you are using this medication ( fexofenadine tablets).
  • Consult your doctor before drinking alcohol or using other medications or natural products that may delay the effects.
  • Consult your doctor if you drink grapefruit juice or eat grapefruit.
  • Use this medication if you are 65 years of age or older ( fexofenadine (Pill) Caution. More side effects may then occur.
  • If you are pregnant, tell your doctor if you want to conceive or breastfeed. You need to have a conversation about the benefits and risks to you and your baby.

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How is this drug (fexofenadine tablets) taken over other drugs?

Use this medicine ( fexofenadine (Tablet) prescribed by your doctor. Read all the information you received. Pay attention to all instructions.

  • Do not take this medicine (Fexofenadine Tablets) with fruit juice. fexofenadine tablet) with fruit juice.
  • Do not take this medicine (tablet) containing magnesium or aluminum at the same time as a stomach acid inhibitor. fexofenadine (Tablet). Consult your own physician or pharmacist.
  • Take with an absolute glass of water.

What if I skip a dose?

  • Take the missed dose as soon as you think of it.
  • If there is almost time for the proper dose, skip the missed dose and return to normal time.
  • Do not take two doses or additional doses at the same time.

What side effects should I notify my doctor about immediately?

Warning/Caution: Despite the fact that it may be rare, some people may have very annoying and sometimes fatal side effects when using the drug. If you have any of the symptoms or signs that may be associated with a fairly annoying side effect, tell your doctor or find medical help right away.

  • Signs of an allergic reaction, such as skin rashes. Birdhouses; itching; skin with or without scar color, swollen, blistered, or fever. ho respectful thoughts; stuffing in the chest or throat. Difficulty breathing, swallowing, or talking. Unusual ho ho s; or, swelling of mouth, face, lips, tongue, or larynx.
  • Blushing.

What are other side effects of Fexofenadine Pills?

All medications can cause side effects. However, almost all have no or only mild side effects. Call your doctor or seek medical assistance if any of these side effects or you are concerned or have not passed.

These are not all side effects that may occur. If you have questions about side effects, call your own physician. Ask your own doctor about side effects.

You can report side effects to the FDA at 1-800-332-1088. https: / / You can report side effects to the FDA at www. FDA.Gov/Medwatch.

If you suspect an overdose:

If you suspect an overdose has occurred, call Anti-Gentrum or seek medical assistance immediately. Be prepared to tell or show them what was taken, how much was taken, and when it happened.

How should I keep and/or throw away Fexofenadine pills?

  • Store at room temperature.
  • Keep in a dry room. Do not store in a bathroom.
  • Store all medications in an unoccupied space. Keep all medications out of the reach of children and pets.
  • Throw away unused or expired medications. Do not rinse out the toilet, flush the toilet or throw it down the sink unless you are told to do so. If you have questions about the best way to throw away your medications, talk to your own pharmacist. There may be a medical program in your area.

Refusing to Use and Be Responsible for Customer Information

  • Call your own doctor if your symptoms or welfare problems do not worsen or if they do.
  • Do not share your medications with other medications and do not take other medications.
  • Some medications may have one package leaflet. Contact your pharmacist. If you have any questions about this medication ( fexofenadine tablet), talk to your own doctor, nurse, pharmacist, or other care provider.
  • If you suspect an overdose has occurred, call Anti-Gentrum or seek medical assistance immediately. Be prepared to tell or show them what was taken, how much was taken, and when it happened.

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Fexofenadine HCl 180 mg

Fexofenadine hydrochloride is considered a histamine H 1-receptor with the chemical title (±)-4- [1 hydroxy-4- [4-(hydroxydiphenylmethyl)-1-piperidinyl]-butbyl], alpha-dimeslo. The correct chemical structure contains

Molecular collection is 538, 13, empirical formula is C 32 H 39 No 4-HCl.

Fexofenadine hydrochloride is a white crystalline powder broken in snow white. It is readily soluble in formaldehyde and ethanol, soluble in chloroform and water, and insoluble in hexane. Fexofenadine hydrochloride is a shellfish and is like a zwitterion in the physical pH aqua medium

Fexofenadine hydrochloride is formulated as an orally-introduced tablet. Each tablet comes in 30, 60, or 180 mg fexofenadine hydrochloride (dose dependent) and appropriate excipients: croscarmellose sodium, magnesium stearate, microcrystalline cellulose, and boaratin-type starch. The Aqua membrane coating of the tablets is prepared from iron oxide concentrate, polyethylene glycol, povidone, silicon dioxide, and titanium dioxide.

Clinical Pharmacological Manipulation Mechanism

Fex phenazine hydrochloride, the most important active metabolite of terfenadine, is an antihistaminic product with selective antagonistic effects on peripheral H 1 receptors. Both enantiomelane of fexofenadine hydrochloride exhibited nearly identical antihistaminic effects. Fexofenadine hydrochloride inhibited antigen-induced bronchospasm in sensitized guinea pigs and inhibited histamine delivery by rat peritoneal fertilizer cells. The clinical significance of these results is unknown. No anti-colling or Alfa-1-addrenoblocking effects were observed in experimental animals. In addition, virtually no calming or other effects on the central nervous system were observed. Studies on the diffusion of radiolabeled tissue in rats show that fexofenadine Do not leak blood brain barrier.

Indications and UseSeasonal allergic rhinitis

Salt salts plant tablets are indicated for the relief of symptoms of seasonal allergic rhinitis in adults and children 6 years of age and older. Effective treatment symptoms are sneezing, nosebleeds, nose/nose/neck/throat, itching/tears/red eyes.

Chronic idiopathic ur measles

For the treatment of uncomplicated cutaneous manifestations of acquired idiopathic ur measles in adults and children 6 years of age and older, salt saline plants are indicated. It is important to reduce itching and blister count.

Saline hydrochloride tablets are contraindicated in patients with known hypersensitivity to one of the ingredients.

Patient Information

Patients using Fexofenadine Hydrochloride should receive correct information.

Fexofenadine hydrochloride tablets are prescribed to illuminate symptoms of seasonal allergic rhinitis or acquired idiopathic ur measles (ur measles). Patients should be instructed to take hydrochloride salts only according to the prescription. Do not exceed the correct dosage. If during the use of fexofenadine, the hydrochloride pills cause unwanted effects, stop using and consult a physician.

This product should not be used in patients with increased sensitivity to the product or in one of its components.

During pregnancy or lactation, patients should be advised that this product should be used only if the possible benefit justifies the possible risk to the fetus or nursing infant.

Patients should be advised to take the tablets with water. Patients should be advised to store the medication in a sealed container in a cool, dry place, out of the reach of children.

Drug Interactions with Erythromycin and Ketoconazole

Fexofenadine has been shown to have the lowest (approximately 5%) metabolism. Most importantly, of fexofenadine plasma concentrations increased when the hydrochloride salt was combined with ketoconazole or erythromycin. of fexofenadine Field fexofenadine did not affect the pharmacokinetics of erythromycin or ketoconazole in two separate studies, fexofenadine Healthy volunteers were treated with 120 mg hydrochloride twice daily (total daily dose 240 mg), 500 mg erythromycin every 8 hours, or 400 mg ketoconazole once daily, under steady-state criteria. Virtually no difference in unnecessary events or QT C interruptions was observed when subjects received fexofenadine hydrochloride alone or in combination with erythromycin or ketoconazole. The results of these studies are summarized in the relevant tables.

Effects on steady state fexofenadine Pharmacokinetics after a total of 7 days of administration fexofenadine 120 mg every 12 hours (twice the recommended dose twice daily) in healthy volunteers (n=24)

Concomitant medications C MAXSS (peak plasma concentration) AUC SS (0-12H) (systemic exposure level)
Erythromycin +82% (0-12H) +109% (500 mg every 8 hours)
(500 mg every 8 hours)
Ketoconazole +135% (500 mg every 8 hours) +164% (400 mg once daily)
(400 mg once daily)
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Changes in plasma levels were within the range of plasma levels achieved in appropriate, well-controlled clinical trials.

The mechanisms of these interactions were evaluated in vitro, in situ, and in vivo animal models. These studies suggest that when combined with ketoconazole or erythromycin, fexofenadine enhance absorption in the gastrointestinal tract. This was observed to increase bioavailability of fexofenadine possibly due to transport effects such as P-glycoprotein; in vivo animal studies continue to show that ketoconazole decreases gastrointestinal secretion in addition to enhancing absorption. fexofenadine Erythromycin, on the other hand, decreases biliary excretion.

Drug Interactions with Antacids

120 mg dose. of fexofenadine Hydrochloride (2 x 60 mg capsules) administered for 15 minutes, followed by reduction of an antacid (MAALOX®) containing aluminum and magnesium. fexofenadine 41% AUC, 43% CMAX. fexofenadine hydrochloride should not be combined with gastric acid inhibitors containing aluminum and magnesium.

Interactions with Fruit Juices

Fruit juices such as grapefruit, orange, and apple can reduce bioavailability and exposure. of fexofenadine The field is based on the results of three clinical studies that combined pharmacokinetic population analysis with the introduction of histamine-induced Katon’s wheel and flare. The size of the wheel and flare was quite large. fexofenadine Grapefruit or orange juice was administered for the hydrochloride compared to water. Based on reports in the literature, the same effect could be extrapolated to other fruit juices such as apple juice. The clinical significance of these studies is unknown. Additionally, a population interference analysis of the aggregate data from the grapefruit and orange juice studies used data from the bioequivalence studies which reduced bioavailability by 36%. of fexofenadine 36% reduction. Thus, maximizing the effect of fexofenadine of hydrochloride (see DOSAGE AND ADMINISTRATION).

Carcinogenesis, mutagenesis, birth defects

Carcinogenic potential and oxidation of reproduction of fexofenadine With the introduction of appropriate terfenadine studies, hydrochloride was considered fexofenadine Exposure to hydrochloride (based on plasma surface subconcentration and time [AUC] values). In an 18-month study in mice and a 24-month study in rats, no substantial signs of carcinogenicity were observed at oral doses of terfenadine up to 150 mg/kg (leading to increased terfenadine exposure). to fexofenadine Approximately 3 and 5 effects than the effect of the very appropriate daily oral doses. of fexofenadine hydrochloride in adults [180 mg] and boys [60 mg] accordingly.

In vitro (bacterial conversion mutations, CHO/HGPRT mutations and rat lymphocyte chromosome aberration tests) and in vivo studies (mouse brain microbial assay), fexofenadine hydrochloride has not produced a mutagenic direction.

In a study on nutritional supplementation in rats, a dose-related decrease in transplantation and structure after transplantation to fexofenadine 180 the effects of the most recommended oral dose on hydrochloride about three times greater than the effects of the most recommended oral dose of mg fexofenadine (hydrochloride). In mice, fexofenadine hydrochloride had no effect on fertility in males or females with average food doses up to 4438 mg/kg (approximately 10 times the maximum adequate oral dose in humans. of fexofenadine 180 mg hydrochloride) based on AUC comparisons.

There was little evidence of teratogenicity in rats or rabbits at oral doses of terfenadine up to 300 mg/kg (which reduced the effects of the most recommended daily oral dose in humans). to fexofenadine Approximately three times the effect of the most recommended daily oral dose in humans and 30 times the exposure of the humane dose of fexofenadine (180 mg hydrochloride) based on AUC comparisons.

In mice, virtually no adverse effects were observed during pregnancy and virtually no teratogenic effects were observed fexofenadine Nutritional doses up to 3730 mg/kg (approximately 15 very adequate oral humane doses) of fexofenadine 180 mg hydrochloride) based on AUC comparisons.

There are no adequate and fully controlled studies in pregnant women. May only be used during pregnancy if the fetal risk is likely to justify it.

Rats exposed to oral doses of 150 mg/kg terfenadine (approximately 3 times the daily oral dose suitable for people. of fexofenadine Based on comparison, 180 mg of hydrochloride in adults of fexofenadine hydrochloride AUCS).

It is not known if fexofenadine Excreted in breast milk. There are no adequate and fully controlled studies for breastfeeding women. Almost all medications vary in breast milk, so caution is advised when footprints appear! fexofenadine Hydrochloride is administered to copper women.

Recommended doses for patients 6 to 11 years are based on comparisons with cross-sectional pharmacokinetic studies of fexofenadine hydrochloride in adult and pediatric subjects and safety profiles. of fexofenadine hydrochloride in both adult and pediatric subjects at doses above the correct dose.

The safety of fexofenadine Tablets containing hydrochloride at a dose of 30 mg twice a week have been demonstrated in 438 pediatric subjects aged 6-11 years with seasonal allergic rhinitis twice a day for 2 weeks. Safety. of fexofenadine Hydrochloride for the treatment of acquired idiopathic ur measles in subjects aged 6-11 years is based on the pharmacokinetics of a cross-section of of fexofenadine hydrochloride and safety profile in adults and children. of fexofenadine In both adult and pediatric subjects at doses above the specified dosage.

The effectiveness of fexofenadine Hydrochloride for the cure of seasonal allergic rhinitis in subjects aged 6 to 11 years was demonstrated in one study (n = 411). fexofenadine Hydrochloride tablets 30 mg twice daily reduced significant joint characteristics compared to placebo, extrapolation of demonstrated performance in subjects 12 years and older, and pharmacokinetic comparisons between adults and children. Efficacy of fexofenadine hydrochloride for the treatment of acquired idiopathic ur measles in patients 6-11 years of age is based on extrapolation of the proven efficacy of of fexofenadine hydrochloride and course of disease in adult patients with this condition, the pathophysiology, and the efficacy of the product in children may be essentially comparable to the efficacy of the course and product in adult patients.

Three studies of medical protection compared 15 mg twice daily (n = 85) with 30 mg twice daily (n = 330). of fexofenadine Placebo (n = 430) was done in children 6 months to 5 years of age. General, fexofenadine hydrochloride was tolerated in these studies. Given the well-known safety profile, no sudden adverse effects were observed. of fexofenadine And possibly side effects in this patient population. (See Side Effects and Clinical Pharmacology.)

Safety and Efficacy of fexofenadine hydrochloride in pediatric patients under 6 years of age has not been established.

Clinical studies of fexofenadine The hydrochloride pills and capsules did not include the required number of described subjects 65 years of age and older to determine if this population would respond differently than younger subjects. Other reported clinical skills showed no difference in response between old and young subjects. This product is known to be quite differentiated by the kidneys, and the risk of toxic reactions to this product may be greater in patients with reduced renal function. Elderly patients are at greater risk of renal impairment, so it is prudent to exercise caution in dose selection and may have a healthier renal prognosis (see CLINICAL PHARMACOLOGY).

Seasonal allergic rhinitis

In a placebo-controlled clinical study of seasonal allergic rhinitis in 2461 subjects aged 12 years and older fexofenadine hydrochloride capsules at doses ranging from 20 mg to 240 mg twice daily, unwanted incidents were comparable in fexofenadine hydrochloride and placebo-coated subjects. All reported unnecessary incidents exceeded 1% of subjects receiving the correct dose of hydrochloride (60 mg capsules twice daily). of fexofenadine hydrochloride (60 mg capsules twice daily), and these occurred more frequently fexofenadine hydrochloride dumps placebo are shown in Table 1.

In a U.S. placebo-controlled clinical study involving 570 subjects aged 12 years and older, adverse effects were comparable to those in the U.S. placebo-controlled clinical study. fexofenadine hydrochloride tablets at doses of 120 or 180 mg once daily, side effects were comparable to those in in fexofenadine hydrochloride and placebo subjects. Table 1 also provides a summary of adverse effects reported by more than 2% of subjects treated with fexofenadine Frequently encounter hydrochloride tablets at a dose of 180 mg once a day fexofenadine hydrochloride, then placebo.

The incidence of adverse effects, including drowsiness, was not dose-related but comparable in age-, sex-, and race-specific subgroups.

Table 1 Undesirable Skills in Subjects 12 Years of Age and Older Speak Up in Placebo-Controlled Clinical Studies on Seasonal Allergic Rhinitis in the United States

Dose twice daily in fexofenadine Capsules at a rate greater than 1% of the dose
Unwanted experience Fexofenadine 60 mg twice daily (n = 679) Placebo twice daily (n = 671)
Viral infections (cold, flu) 2, 5%. 1, 5% Nausea
Nausea 1, 6% Nausea 1, 5% Nausea
DysmeLORHEA 1, 5% Nausea 0, 3% Drowsiness
Drowsiness 1, 3% Drowsiness 0, 9% Dyspepsia
Indigestion 1, 3% Drowsiness 0, 6%
Fatigue 1, 3% Drowsiness 0, 9% Dyspepsia
Dosed once daily in fexofenadine Hydrochloride tablets with doses greater than 2%.
Unwanted experience Fexofenadine 180 mg once daily (n = 283) Placebo (n = 293)
Headache 10, 6%. 7, 5% Upper respiratory tract infection
Upper respiratory tract infection 3, 2% (n = 293) 3, 1%
Back pain 2, 8% 1, 4%

Frequency and size of laboratory disorders were similar in in fexofenadine hydrochloride and placebo-coated subjects.

Table 2 provides a summary of adverse effects in subjects 6 to 11 years reported in more than 2% of treated subjects fexofenadine A placebo-controlled study of seasonal allergic rhinitis in the United States and Canada has hydrochloride tablets at a dose of 30 mg twice daily. fexofenadine hydrochloride, then placebo.

Table 2 Side effects reported in placebo-controlled studies of seasonal allergic rhinitis in pediatric subjects aged 6-11 years in the United States and Canada at ≥2%.

Unwanted experience Fexofenadine 30 mg twice daily (n = 209) Placebo (n = 229)
Headache 7, 2%. 6, 6% (n = 229)
Injury 2, 9% Injury 1, 3% Drowsiness
Cough 3, 8%. 1, 3% Drowsiness
High temperature 2, 4% 0, 9% Dyspepsia
Pain 2, 4% 0, 4%
Middle ear infection 2, 4% 0, 0% 0, 0
Upper respiratory tract infection 4, 3% (1, 7%) 1, 7%

Three studies were conducted on 845 children over a period of 6 months, 15 mg twice daily (n = 85), compared to placebo, 30 mg twice daily (n = 330) for the experimental formulation (n = 430). of fexofenadine Compared to placebo (n = 430). General, fexofenadine hydrochloride was tolerated in these studies. Given the well-known safety profile, no sudden adverse effects were observed. of fexofenadine and possibly side effects in this patient population. (See WARNINGS for pediatric use.)

Chronic idiopathic ur measles

Unnecessary incidents reported by subjects aged 12 years and older in a placebo-controlled study of acquired idiopathic ur measles were comparable to those reported in a placebo-controlled study of seasonal allergic rhinitis. In a placebo-controlled clinical study of acquired idiopathic ur measles, 726 patients aged 12 years and older received fexofenadine hydrochloride tablets given twice daily in doses ranging from 20 to 240 mg had comparable adverse effects. in fexofenadine patients who received hydrochloride and placebo. Table 3 provides a summary of unnecessary incidents for subjects aged 12 years and older reported by more than 2% of subjects who used the product. fexofenadine In controlled clinical studies in the United States and Canada, the more common twice-daily 60 mg hydrochloride tablets were 60 mg fexofenadine hydrochloride, then placebo.

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A placebo-controlled clinical study in the U.S. included 167 subjects aged 12 years and older. fexofenadine received 180 mg hydrochloride tablets and had comparable unwanted symptoms in fexofenadine subjects receiving hydrochloride and placebo. Table 3 also provides a summary of unwanted symptoms reported by more than 2% of subjects who received the product. fexofenadine Frequently encounter hydrochloride tablets at a dose of 180 mg once a day fexofenadine hydrochloride, then placebo.

The safety of fexofenadine Hydrochloride in the treatment of acquired idiopathic ur measles in children 6 to 11 years of age, based on protective profile. of fexofenadine Hydrochloride in adults and young adults at doses above the correct dose (see Pediatric Uses).

Table 3: Idiopathic narcotic paralysis with adverse effects reported in patients 12 years and older in placebo-controlled studies

Twice-daily administration fexofenadine In U.S. and Canadian studies, the rate of hydrochloride is greater than 2%.
Unwanted experience Fexofenadine 60 mg twice daily (n = 191) Placebo (n = 183)
Indigestion 4, 7%. 4, 4% Muscular pain
Muscle pain 2, 6% Muscle pain 2, 2%
Back pain 2, 1% 1, 1%
Dizziness 2, 1% 1, 1%
Limb pain 2, 1% 0, 0% 0, 0
Administer once daily fexofenadine Hydrochloride in US studies at levels above 2%.
Unwanted experience Fexphenadine 180 mg once daily (n = 167) Placebo (n = 92)
Headache 4, 8%. 3, 3% (n = 92)
Nasopharyngitis 2, 4% 2, 2%
Infected upper respiratory tract 2, 4% 2, 2%

Actions reported during controlled clinical examinations by subjects with seasonal allergic rhinitis have been reported occasionally during postmarketing surveillance, with less than 1% and an incidence of idiopathic ur measles similar to placebo: insomnia, stress, sleep disturbances or paronychia rarely, skin rash, ur measles, pruritus, hypersensitivity reactions have been reported with these symptoms including angioedema, chest palpitation, dyspnea, blushing, and systemic anaphylaxis.

Reports of fexofenadine Overdose due to hydrochloride has not been investigated with limited information. Dizziness, drowsiness, and dryness have been reported in the last place.1 Dosage of fexofenadine A maximum of 800 mg hydrochloride (6 healthy volunteers at this dose level) was administered twice a month for up to 690 mg (3 healthy volunteers at this dose level) or once a day for up to 240 mg (234 healthy volunteers at this dose level) compared to placebo, without clinically significant adverse effects The product was administered without cause of any clinically significant adverse effects.

In the event of an overdose, consider the usual means of immediate product removal. Symptomatic and supportive treatment is recommended. Following administration of terfenadine, product was not effectively removed by hemodialysis. fexofenadine Most important active metabolite of terfenadine from blood (up to 1.7% removed).

At doses of perol of fexofenadine HCl of up to 5000 mg/kg in mice exceeded the most appropriate daily oral dose in adult mice and more than 200 above the optimal daily oral dose in children of Mg/m 2 base and up to 5000 mg in rats (rat ( Rattenb 230 one more than the most appropriate daily oral dose in adults and 400 more than the most appropriate daily oral dose in MG/M 2-based persons). In addition, there were no clinical signs of toxicity or gross pathological findings observed. Almost no signs of toxicity were observed at oral doses up to 2000 mg/kg (300 above the most appropriate daily oral dose for adult humans and 530 above the most appropriate daily oral dose for mg/m 2 base children).

Medication and Management

Seasonal allergic rhinitis mature and young children over 12 years of age

The recommended dosage of hydrochloride salt is 60 mg twice daily or 180 mg with water once daily. A dose of 60 mg once daily is recommended as a starting dose for patients with impaired renal function (see Clinical Pharmacology).

Children 6 to 11 years of age

The correct dosage of fexofenadine hydrochloride is 30 mg twice daily with water. A starting dose of 30 mg once daily is recommended for pediatric patients with impaired renal function (see Clinical Pharmacology).

Chronic idiopathic ur measles

Adults ≥ 12 years and young children

The recommended dosage of hydrochloride salt is 60 mg twice daily or 180 mg with water once daily. A dose of 60 mg once daily is recommended as a starting dose for patients with impaired renal function (see Clinical Pharmacology).

Children 6 to 11 years of age

The correct dosage of fexofenadine hydrochloride is 30 mg twice daily with water. A starting dose of 30 mg once daily is recommended for pediatric patients with impaired renal function (see Clinical Pharmacology).

Fexofenadine Hydrochloride 30 mg is available in a bottle of HDPE 100 (NDC 66993-106-02) with a slider/wax lined polypropylene screw cap with heated foil.

Fexofenadine hydrochloride 60 mg tablets are available in HDPE 100 (NDC 66993-107-02) bottles with pulp/wax lined polypropylene screw caps with heated foil and HDPE 500 bottles (NDC 6993-104-04-04 and HDP E-02) available in. Polypropylene. Pulp/wax lined screw cap with heated foil in the seal.

Fexofenadine Hydrochloride 180 mg available in HDPE 100 bottles (NDC 66993-109-02) with pulp/wax lined polypropylene screw caps with heated foil inner seal and HDPE 500 bottles (NDC 66993-09-04) Available in. Pulp/wax lined with heated foil inner seal.

Fex Phenazine Hydrochloride tablets are covered with a peach membrane. The tablets have the correct original individual numbers: the 30 mg tablets have 03 on one side, the 60 mg tablets have 06 on one side and 018 on the other.

Save the hydrochloride salts at a controlled room temperature of 20-25°C (68-77°F). (See USP Controlled Room Temperature). The hydrochloride salts should be protected from excess moisture.

Hertz. manufactured August 2006 by: Sanofi-Aventis U. S. LLC. Bridgewater, NJ 08807 USA.

Made: Prasco Laboratories Cincinnati, OH 45249 USA

©2006 Sanofi-Aventis U. S. LLC

Image markers & lt; Pran & gt;, prescription drugs, freely available medications, vitamins, and herbal products. Not all interactions between drugs are mentioned here.

Label Image

Fexofenadine

Generic name: fexofenadine [Fex-hoh-fen-a-deen] Brand: Allegra 12 Hour Allergy, Allegra 24 Hour Allergy, Allegra Allergy, Allegra Allergy, Allegra OTC, Allah Ace,. 8 brands Allergy Relief (Fexphenadine HCl) Allergy Relief (Fexphenadine HCL), Pediatric Allergy, Pediatric Allergy, Pediatric Dosing Allegra ODT: Oral Suspension All Oral tablets; orally disintegrating tablets class of drugs: antihistamines

Carmen Fuchs Diagnosis, Bpharm. last updated on January 31, 2023.

What is fexofenadine ?

Fexofenadine is an antihistamine that can be used to treat signs of allergy (including SEN fever) in adults and children.

Fexofenadine is also used to treat itchy skin and hives caused by a condition called idiopathic ur measles in adults and children at least 6 years old.

Fexofenadine works selectively on histamine-1 sensors that are in our body but not in the central nervous system – they are called peripheral histamine sensors. Because it works on these sensors, fexofenadine it causes drowsiness much faster than some older antihistamines.

Histamine is a chemical excreted by fertilizer cells in response to allergens and is responsible for nearly all signs of allergy, including eyes, runny nose, sneezing, and itching. Fexofenadine binds to histamine sensors, preventing histamine from acting on these sensors and reducing allergy symptoms.

Numerous brands and forms are available of fexofenadine available.

Fexofenadine was approved by the FDA in 1996.

Related/similar substances

Warning.

Do not take fexofenadine Fruit juices (apple, orange, grapefruit, etc.).

Before taking this medication

You should not use fexofenadine If you are allergic to it.

Ask your doctor or pharmacist if fexofenadine Is it safe to use?

Ask your doctor to use it fexofenadine If you are pregnant or breastfeeding.

Elderly people may be more sensitive to the effects of this medication; if you are over 65 years of age, ask your doctor before taking it. fexofenadine .

This medication can retain phenylalanine and may be harmful if you have phenylketonuria (PKU).

How should I take fexofenadine ?

Take fexofenadine As indicated on the label or as prescribed by your doctor.

Always follow the directions on the drug label about giving your child cough and cold preparations.

  • Ask your doctor before getting data on fexofenadine Liquid to children under 2 years of age.
  • Disintegrating (melting) pills are not for use in children under 6 years of age.
  • 12-hour and 24-hour forms of fexofenadine Not for use in babies under 12 years of age.

Take this medicine only with water.

Take the disintegrating pills on an empty stomach.

Shake the oral suspension (liquid) before measuring the dose. Use the dosing cup supplied or use the dosing device on the medication (without a kitchen spoon).

fexofenadine orally disintegrate the footsteps from the package just before keeping the pills. Place the pill on the tongue and allow it to unwind without chewing. Swallow a certain number of times while the pill is dissolving.

If complaint does not improve or gets worse, call your own doctor.

Store fexofenadine In original package at room temperature, away from moisture and heat. Do not show water-based medicine.

What happens if I overdo the dosage?

Fexofenadine is used as needed. If following a dosing schedule, skip the missed dose. Do not use two doses at the same time.

What happens if I overdose?

Find appropriate medical help or call the Poison Line at 1-800-222-1222.

Overdose symptoms of fexofenadine May cause dry mouth, dizziness, and drowsiness.

What should I ignore fexofenadine ?

Do not take fexofenadine Fruit juices (e.g., apple, orange, grapefruit). These juices have a good chance of making it harder for the body to record. fexofenadine .

Do not take stomach acid inhibitors around 2 hours before or after fexofenadine . Do not use fexofenadine At the same time as stomach acid inhibitors containing magnesium or aluminum.

Ask your doctor or pharmacist before using any other cough or cold that may contain similar ingredients.

Fexofenadine Side Effects

Find emergency medical help if you have symptoms of an allergic reaction to fexofenadine Birdhouses; rough breathing; swelling of the face, lips, tongue, or throat.

Fexofenadine can cause nonsense side effects. Stop using it. fexofenadine And call your doctor immediately if you are suffering from any of these side effects:

  • Flu-like symptoms (fever, shakiness, unusual fatigue);.
  • New or worsening cough; or
  • Pain; or
  • Ear infection signs ear pain or absolute sensation, hearing difficulty, small stones from the ear, baby bother.

Common side effects of fexofenadine may include:

  • Headache; or
  • Back pain; or
  • Freezing symptoms; breathless nose; sinus pain; sore throat.

This is not an absolute list of side effects; other side effects may occur. Ask your doctor about side effects; you can report side effects to the FDA at 1-800-FDA-1088.

other medications affected. fexofenadine ?

Using fexofenadine Other medications that make you drowsy may exacerbate this effect. Ask your doctor before using opioids, sleeping pills, muscle relaxants, or medications for anxiety or aggression.

Ask your doctor or pharmacist before using fexofenadine Other Medication Details:

This list is not complete. Other medications may affect you fexofenadine Prescription drugs and freely available medications, vitamins, and herbal products. Not all possible interactions between drugs are mentioned here.

Where can I get more information?

Keep this and all other medications out of the reach of children and do not share your medications with other medications.

More about fexofenadine

  • Check for interactions.
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  • Pregnancy
  • Class of drugs: antihistamines
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For more information

Always consult your physician to ensure that the information on this page is used in your own case.

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Family Medicine

Family MedicineIn 2024 our team of doctors and nurses provide a comprehensive range of family planning services. Our doctors have expertise in antenatal care, preconception planning, and STD checks. Contraceptive advice including Mirena and Implanon insertion is available.

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Alex Koliada, PhD

Alex Koliada, PhD

Alex Koliada, PhD, is a well-known doctor. He is famous for his studies of ageing, genetics and other medical conditions. He works at the Institute of Food Biotechnology and Genomics NAS of Ukraine. His scientific researches are printed by the most reputable international magazines. Some of his works are: Differences in the gut Firmicutes to Bacteroidetes ratio across age groups in healthy Ukrainian population [BiomedCentral.com]; Mating status affects Drosophila lifespan, metabolism and antioxidant system [Science Direct]; Anise Hyssop Agastache foeniculum Increases Lifespan, Stress Resistance, and Metabolism by Affecting Free Radical Processes in Drosophila [Frontiersin].
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