Cintar

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Cintar

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Cintar

What is Cintar?

Cintar is a pharmacological treatment used primarily in the management of gastrointestinal motility disorders. It belongs to a class of medications known as prokinetics, which are designed to enhance the movement of food and waste through the digestive tract.

Mechanism of Action

The active component in Cintar works by stimulating specific receptors in the gut wall. This stimulation increases the release of acetylcholine, a neurotransmitter that triggers the muscles in the digestive system to contract. By improving the coordination and strength of these contractions, the medication helps to accelerate gastric emptying and reduce the transit time of material through the esophagus and stomach.

Primary Uses

Cintar is typically utilized to address symptoms associated with a slowed digestive process. These clinical applications include:

  • Gastroesophageal Reflux Disease (GERD): Helping to reduce the upward flow of stomach acid into the esophagus by strengthening the lower esophageal sphincter and clearing the stomach more efficiently.
  • Functional Dyspepsia: Alleviating sensations of fullness, bloating, and upper abdominal discomfort after eating.
  • Gastroparesis: Assisting in the management of delayed stomach emptying, which can be caused by various underlying metabolic or systemic conditions.

Clinical Role

As a prokinetic agent, Cintar focuses on the mechanical function of the digestive system rather than altering the acidity of the stomach. It is often integrated into a broader management plan that may include dietary adjustments and lifestyle changes to improve overall digestive health and comfort.

What side effects are possible with Cintar?

Possible Side Effects and Safety Information

Cintar's safety profile is defined by officially documented adverse reactions classified by frequency and system-organ class, as compiled from government regulatory sources. The most frequently encountered adverse reactions typically involve the Central Nervous System (CNS) and Gastrointestinal (GI) systems.

Frequency of Adverse Reactions

Side effects are officially classified using frequency bands based on clinical data:

  • Common (May affect up to 1 in 10 people): Somnolence (drowsiness), fatigue, headache, dizziness, dry mouth, nausea, and pharyngitis (sore throat).
  • Uncommon (May affect up to 1 in 100 people): Asthenia (extreme weakness), malaise, agitation, pruritus (itching), and rash.
  • Rare (May affect up to 1 in 1,000 people): Hypersensitivity reactions (allergic reactions), convulsions, confusion, abnormal liver function, and increased weight.
  • Very Rare (May affect up to 1 in 10,000 people): Syncope (fainting), tremor, fixed drug eruption, and urinary retention.

Serious Adverse Reactions and Safety Constraints

The official label documents rare but clinically significant adverse reactions, primarily categorized as severe hypersensitivity reactions, which include anaphylaxis and angioedema (swelling). Convulsions and reports of abnormal liver function are also formally documented as rare adverse events.

Specific safety considerations are noted for certain populations. Clearance of the medicine is decreased in patients with renal or hepatic impairment, generally necessitating dose adjustment consideration. Caution is also advised for patients who have risk factors for urinary retention or who are epileptic, due to the potential for increasing these risks.

Furthermore, the label notes that severe itching (pruritus) has been reported to occur following the discontinuation of long-term daily use.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose with Cetirizine Dihcl (Cintar) is formally documented in regulatory sources and requires immediate attention due to the risk of severe complications.

Documented Manifestations and Severe Outcomes

Overdose presentations primarily involve effects on the central nervous system (CNS). Common documented manifestations include pronounced somnolence, drowsiness, fatigue, and confusion. In pediatric patients, initial signs may involve restlessness and irritability before the onset of depression. Other reported physiological effects include tachycardia (fast heart rate), urinary retention, and diarrhea.

Severe or life-threatening outcomes described in official documents are rare but can include seizures (convulsions), coma, and severe cardiac effects.

Required Emergency Actions

When an overdose is suspected, government regulatory guidance mandates seeking immediate medical attention and contacting a Poison Control Center right away.

Urgent medical help must be sought immediately if the affected person collapses, has a seizure, is experiencing trouble breathing, or cannot be awakened.

Management procedures are strictly symptomatic and supportive, as official prescribing information confirms there is no known specific antidote for Cetirizine Dihcl. Regulatory information also notes that the drug is not effectively removed by dialysis.

Therapeutic Uses of Cintar

What Cintar Treats: Main Uses and Benefits

Cintar is commonly used to help with symptoms related to heightened physiological activity caused by allergies, providing support that helps ease the overall symptom burden. It is relevant in conditions characterized by periods of heightened symptoms and systemic discomfort.

Symptom Management for Allergies and Hives

Cintar is applied across domains where additional symptomatic support is needed. It is considered relevant for conditions involving episodic or fluctuating manifestations such as seasonal hay fever, persistent year-round allergies, and recurrent Chronic Idiopathic Urticaria (hives). It is commonly used to help with symptom clusters that may become disruptive, including sneezing, runny nose, itching of the eyes or throat, and symptoms related to skin itching (pruritus) that interfere with daily functioning. This use contributes to easing the overall symptom load during symptomatic periods.

“This therapeutic use is relevant when supportive symptom management is appropriate, assisting with relief from the noticeable physiological strain of allergic episodes.”

For patients managing recurrent discomfort, this therapeutic use may assist with maintaining a sense of stability when symptoms are more noticeable during difficult episodes.


Quick Fact: Relief for Rhino-Ocular and Dermal Symptoms Cintar is applied for managing the two key symptom categories of allergies: discomfort in the rhino-ocular areas (sneezing, runny nose, itchy eyes) and dermal manifestations (itching and hives).

Eligibility and Restrictions for Use

Who Can and Cannot Use Cintar?

Official regulatory documents strictly define the patient populations eligible to use Cintar (Cetirizine Dihcl), primarily based on age, organ function, and known sensitivities. The medicine is contraindicated for patients with a known hypersensitivity to cetirizine, any of the excipients, hydroxyzine, or other piperazine derivatives. Use is also absolutely prohibited for patients with severe renal impairment (end-stage renal disease, CrCL below 10–15 mL/min).

Population Eligibility Status Regulatory Classification (Examples)
Contraindicated Severe Renal Impairment, Hypersensitivity to Hydroxyzine
Conditional Use Moderate Renal Impairment, Predisposition to Urinary Retention
Not Recommended Children under 6 years (for tablet form), Lactating Women

Age-related eligibility covers adults and adolescents, and children as young as 6 months for liquid formulations under specific conditions. However, the tablet form is not recommended for children under six, as the dose cannot be adjusted appropriately. Conditional use is required for patients with moderate renal impairment or a history of conditions predisposing to urinary retention or convulsions; in these groups, official labeling recommends caution. Use during pregnancy and lactation is generally restricted and advised with caution.

What should I know about interactions with other medicines?

Cintar (cetirizine) is a second-generation antihistamine with a low potential for significant drug interactions. However, it is essential to inform your healthcare provider of all other medications, supplements, and products you are using.

Medications that Increase Sedation Risk

The most important interaction is the potential for additive effects with substances that depress the central nervous system (CNS). Concurrent use may increase side effects such as drowsiness, reduced alertness, and impaired psychomotor function.

  • Alcohol: Avoid or severely limit alcohol consumption while taking this medicine.
  • CNS Depressants: Use with caution when taken with other agents that cause drowsiness. These include, but are not limited to, tranquilizers, sedatives, prescription pain medications (opioids), and certain anti-anxiety drugs (benzodiazepines).

Other Drug Interactions

Clinical studies have generally shown no major drug interactions with Cintar when used at the recommended dose.

Concomitant Drug Interaction Note
Theophylline (400 mg/day) A minor, non-clinically significant 16% decrease in Cintar clearance (elimination from the body) was observed. Theophylline's action was not affected.
Azithromycin, Erythromycin, Ketoconazole No clinically significant pharmacokinetic interactions have been found.

Food and Laboratory Tests

Food does not affect the overall amount of Cintar absorbed (AUC), meaning it can be taken with or without a meal. However, a meal may slightly delay the time it takes to reach maximum concentration in the blood. Like all antihistamines, Cintar can inhibit the response to allergy skin tests, and a washout period of approximately 72 hours (3 days) is generally recommended before testing.

Mechanism of Action

Cintar’s primary mechanism of action involves functioning as a selective antagonist at the Histamine H1-receptors ( H1R), which are expressed on peripheral cells, including endothelial cells and sensory nerve endings. By binding to and occupying these receptors, the drug blocks the attachment of endogenous histamine, thereby suppressing the downstream Gq/11 signaling cascade. This blockade modulates local vascular dynamics by counteracting histamine-induced vasodilation and reducing the resulting increase in capillary permeability.

Beyond this receptor action, the mechanism also involves H1R-independent modulation of the cellular inflammatory cascade. This secondary effect suppresses the migration and chemotaxis of eosinophils and restricts the expression of adhesion molecules (VCAM-1 and ICAM-1) on endothelial surfaces, limiting cellular infiltration within peripheral tissues.

Furthermore, the chemical properties of Cetirizine Dihcl ensure peripheral selectivity due to minimal crossing of the Blood-Brain Barrier (BBB). This targeted distribution concentrates the H1 antagonism on peripheral sites, resulting in minimal receptor occupancy within the central nervous system.

Dosage and Administration Information

Cintar, which contains Cetirizine Dihcl, is administered either through the oral route (as a tablet, solution, or syrup) or via the intravenous route as an injectable solution. The standard adult regimen for oral administration is 10 mg taken once daily, although an alternative starting dose of 5 mg once daily may be used in certain contexts. The total dose does not exceed 10 mg in any 24-hour period.

The timing of oral administration is flexible: it may be taken with or without food, as absorption is not significantly affected by food intake. Patients using liquid forms use a calibrated measuring device, such as a syringe or spoon, to ensure accurate dosing.

Dose modification is applied for specific populations. For older adults, a 5 mg once-daily dose is often designated. Furthermore, the dose is adjusted (typically reduced) for individuals with moderate to severe renal impairment. In the case of the injectable formulation, the dose is administered by a healthcare professional as a slow intravenous push over 1 to 2 minutes. Use patterns include both short-term administration for acute symptoms and long-term use for managing chronic conditions.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Cetirizine Dihcl (Cintar)

The research landscape for Cetirizine Dihcl is substantial, built primarily on Randomized Controlled Trials (RCTs) and validated by Systematic Reviews. Regulatory authorities rely on these controlled studies to establish the conditions or populations for which the medicine has been evaluated. The following overview describes what the evidence has explored, what outcomes were measured in the studies, and what limitations or uncertainties remain.


Evidence for Use in Seasonal and Perennial Allergic Rhinitis

Research has explored Cetirizine Dihcl in studies relevant to symptoms associated with both seasonal hay fever and year-round, perennial allergies. These trials utilized controlled, randomized designs to evaluate changes in measured outcomes over defined time intervals. The primary outcomes related to physical discomfort that were monitored in these studies included measurements of sneezing, runny nose, itchy eyes, and nasal irritation. Findings describe patterns observed in the studies where groups using the study medicine were observed to have measured outcomes that varied from groups using a non-treatment (placebo) approach over the study period. While the evidence contributes to understanding short-term symptom patterns, long-term effects are not fully established.


Evidence for Use in Chronic Spontaneous Urticaria (Hives)

Cetirizine Dihcl was also studied for use in conditions characterized by fluctuating manifestations, such as chronic spontaneous urticaria (hives). This research examined the impact on outcomes linked to inflammatory or irritative states, primarily focusing on reducing the occurrence of wheals and the severity of itching. Research has explored the use of doses above the standard licensed amount in specific studies focusing on populations with persistent symptoms. These higher-dose findings described measured outcomes that varied in some populations, and the studies reported an increase in somnolence (drowsiness) observed during the study period. However, for these higher-than-standard uses, the comparative evidence is lacking and the sample sizes were modest.


Evidence in Specific Patient Groups and Research Gaps

Studies have monitored pharmacokinetic changes in older individuals. Findings indicate that the clearance rate for the medicine is documented as slower in older adults, a pattern noted in relation to changes in kidney function. Data for this group remain limited. Furthermore, post-marketing surveillance reports highlight that long-term effects are not fully established, particularly regarding the potential for rebound itching observed in some studies after prolonged daily use was discontinued.

Frequently Asked Questions (FAQ)

Common questions about Cintar (FAQ)

Q: Does Cintar start working right away, or does it take time?

A: According to official product information, the onset of action for Cintar is generally observed. Clinical studies describe the onset of action as generally observed within 20 to 60 minutes following oral administration.


Q: Is it true that Cintar is not recommended for people with kidney problems?

A: Regulatory documents state that Cintar is contraindicated (absolutely prohibited) for individuals diagnosed with severe kidney problems, specifically those with a creatinine clearance ( CrCL) below 10-15 mL/min. For individuals with moderate kidney issues, dose modification is generally mandated in official guidelines due to the slower elimination rate documented in these populations.


Q: Does Cintar interact with common over-the-counter pain relievers?

A: Official interaction reports focus on substances that affect the central nervous system, such as alcohol, or specific prescription medicines. The regulatory documents do not generally list specific interactions for every common over-the-counter pain reliever, and no clinically significant pharmacokinetic interactions have been explicitly noted in the official drug-drug interaction studies.


Q: Does Cintar make you feel tired or drowsy?

A: Yes, regulatory labeling documents that somnolence, which means drowsiness, is categorized as a Common adverse reaction. This means it may affect up to 1 in 10 people taking the medicine. Fatigue is also listed in the same frequency category.


Q: What is the purpose of the initial testing sometimes required before starting Cintar?

A: Regulatory prescribing information indicates that antihistamines like Cintar can interfere with the results of allergy skin testing. For accurate results, a washout period, which is typically 72 hours, may be recommended before the test is performed.


Q: Can I drink alcohol while I'm on Cintar?

A: The official product label carries a specific warning that the use of alcohol is required to be avoided or severely limited while taking Cintar. This caution is issued because alcohol can increase the potential for additive effects with the medicine, leading to greater drowsiness or reduced alertness.


Q: Does Cintar need to be taken with food, or does it not matter?

A: Official regulatory documents state that Cintar can be taken with or without food. While consuming it with a meal may slightly delay the time it takes to reach maximum concentration in the blood, the overall amount of the medicine absorbed is not affected.


Q: Does Cintar cure the condition, or just manage the symptoms?

A: Regulatory indications describe the purpose of Cintar as providing relief from symptoms associated with allergic conditions, such as sneezing, runny nose, and itching. The medicine is not officially described in regulatory documents as a cure for the underlying condition.


Q: What should I do if I miss a dose of Cintar?

A: Official patient instructions state that a missed dose is generally taken as soon as it is remembered. However, if it is nearly time for the next scheduled dose, the regulatory guidance is documented as skipping the forgotten dose to resume the regular schedule.


Q: Can Cintar affect my ability to drive or operate machinery?

A: Due to the documented potential for side effects like drowsiness (somnolence) and dizziness, the official labeling carries a specific warning that individuals must exercise caution regarding activities that require full mental alertness, such as driving or operating machinery, until they are aware of their response to the medicine.


Q: Is there a generic version of Cintar available?

A: Yes, the active ingredient in Cintar is Cetirizine Dihcl. Regulatory information confirms that generic versions of this active substance are widely available for purchase.


Q: What happens if I accidentally take more Cintar than prescribed?

A: Official regulatory documents describe the symptoms of over-ingestion. Taking a significantly higher amount than prescribed may lead to symptoms that include somnolence (drowsiness), tiredness, confusion, headache, and agitation.


Q: Can men and women use Cintar in the same way?

A: Regulatory documentation confirms that the standard dosage instructions and contraindications for Cintar are based on factors like age and the status of kidney or liver function. The official labeling does not specify different dosing or usage requirements for adult men and women.


Q: Does Cintar need to be tapered off, or can I stop suddenly?

A: Regulatory reports highlight that severe itching (pruritus) has been documented to occur following the abrupt discontinuation of long-term daily use of the medicine. While this specific effect is noted, the official label does not provide instructions for tapering the dose.


Q: What happens if I miss several doses of Cintar?

A: Official patient information focuses on what to do when a single dose is missed. If several doses have been missed, the regulatory requirement is that the course of action be determined in accordance with the original prescribing information.


Q: Why is the dosage different for different people taking Cintar?

A: Regulatory documents require dosage modification for specific populations to account for differences in how the body processes the medicine. This includes individuals over 65 years of age and those with reduced kidney function (renal impairment), whose rate of drug elimination is officially documented as slower.


Q: Does Cintar affect sleep patterns?

A: Regulatory documents list the Central Nervous System effects of somnolence (drowsiness) and fatigue as Common adverse reactions. While these effects can indirectly affect rest, the official label does not detail the medicine’s effects on the general structure or quality of sleep patterns.

How should Cintar be stored and disposed of?

How to Store and Dispose of Cintar?

Cintar (Cetirizine Dihcl) must be stored according to requirements documented in official regulatory labeling to maintain its stability and effectiveness.

Storage Conditions

The medication must be stored at controlled room temperature, generally below 30°C (86°F), and kept in its original container with the lid tightly closed. The product must be protected from excessive heat and moisture. Liquid forms, such as the oral solution or syrup, are explicitly restricted from being frozen. For all formulations, it is a mandatory requirement to keep the medicine out of the sight and reach of children.

Disposal Requirements

Official instructions require that unused or expired Cintar must not be disposed of via household wastewater (such as flushing down the toilet or sink) or routine household trash. Disposal must adhere to local regulatory requirements, typically by returning the medicine to a pharmacy or an authorized collection program.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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