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Revlimid 25mg

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Revlimid 25mg

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Medically reviewed

Laura Arias

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.

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Overview of Revlimid 25mg

Quick Facts

Property Description
Active ingredient Lenalidomide
Form Hard capsule, for oral administration
Pharmacological class Immunomodulatory Agent (IMiD), Antineoplastic Agent
General purpose To modulate the immune system and inhibit abnormal cell growth
Origin Synthetic compound; analogue of thalidomide
Status Prescription-only medicine (Rx)

What is Revlimid 25mg and What Pharmacological Class Does it Belong To?

Revlimid 25mg is the trade name for a medicine containing the active substance Lenalidomide, which is provided via a prescription. It belongs to a specialized group of treatments known as Immunomodulatory Agents (IMiDs). The drug is categorized as an antineoplastic agent as its actions are directed at the growth and survival of abnormal cells in the body.

Lenalidomide is a synthetic compound derived chemically as an analogue of thalidomide, specifically refined as a phthaloyl-glutamic acid derivative to provide targeted therapeutic action. This unique synthetic origin gives it a distinct mechanism of action within its class, a differentiating factor from older therapies.

Lenalidomide: Composition, Form, and General Purpose

The medicine is a single-active-ingredient product featuring Lenalidomide as its sole active component, delivered in an oral dosage form as a hard capsule. This formulation is designed for the oral route of administration, allowing the medicine to be absorbed into the bloodstream and act systemically throughout the body. The fundamental purpose of Lenalidomide therapy is to establish a healthier cellular environment in managing certain blood cancers.

This therapeutic effect is achieved through a three-fold action: modulating the immune system, interfering with the growth and survival of abnormal cells, and limiting the development of new blood vessels (anti-angiogenesis). This combination of effects makes it an agent for altering tumor immunity and proliferation. This strategic, multi-faceted approach forms the core of its utility in addressing conditions related to cell proliferation.

Regulatory References

  1. National Institutes of Health (NIH)
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What side effects are possible with Revlimid 25mg?

Possible side effects and safety information

The official safety profile of Lenalidomide (Revlimid), as documented by international regulatory bodies, is structured around several critical adverse reaction categories and safety constraints. All listed effects and classifications are derived strictly from government regulatory prescribing information.


Frequency-Classified Adverse Reactions

Adverse effects are grouped by their frequency as documented in clinical trials and official labeling:

Classification Examples of Documented Effects (System-Organ Class)
Very Common (ge 1/10) Neutropenia, Thrombocytopenia (Blood); Diarrhea, Constipation (Gastrointestinal); Fatigue, Asthenia (General); Rash (Skin).
Common (ge 1/100 to < 1/10) Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE) (Vascular); Peripheral Neuropathy (Nervous System); Hypothyroidism (Endocrine).

Serious Adverse Reactions and Safety Constraints

Regulatory documents highlight several potentially life-threatening or serious reactions:

  • Serious Hematologic Toxicity: Severe myelosuppression, including Grade 3/4 Neutropenia and Thrombocytopenia, is a major documented risk. These effects are often noted to occur early in the course of treatment and require surveillance of blood counts.
  • Thromboembolic Events: Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) are officially classified as common serious vascular risks, particularly when Lenalidomide is used in combination with Dexamethasone.
  • Known Human Teratogen: Lenalidomide is strictly classified as a Known Human Teratogen by regulatory authorities. This restriction necessitates special restricted distribution programs globally to prevent any use during pregnancy due to the high risk of severe birth defects.
  • Organ System Risks: Risks of Serious Infections, Hepatotoxicity (liver damage), and the potential for Secondary Primary Malignancies (SPMs) are documented in the safety profile, with SPMs associated with long-term exposure.

Population-Specific Safety Notes

The label includes specific safety considerations for patients with renal impairment, as the drug is primarily cleared by the kidneys, and for older adults (ge 65 years), who may be more susceptible to certain adverse effects.

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Overdose and Emergency Response

Overdose and When to Seek Help

There is limited clinical data on the effects of acute overdose with Revlimid (lenalidomide). In clinical studies, some patients received lenalidomide doses up to 150 mg once daily, or 400 mg as a single dose. These higher exposures were generally associated with an increase in known dose-limiting toxicities, particularly hematologic effects like neutropenia (low white blood cells) and thrombocytopenia (low platelets).

If you believe you have taken more than the prescribed dose of Revlimid 25 mg, it is critical to seek immediate medical attention. Contact emergency services or go to the nearest hospital emergency room. Management of a lenalidomide overdose is typically supportive and involves careful monitoring of the patient for signs of toxicity.

When to Seek Emergency Help

Even while taking the prescribed dose, certain serious adverse effects require urgent medical evaluation. Seek immediate help if you experience:

  • Signs of a Blood Clot (Thrombosis): Sudden shortness of breath, chest pain, or swelling, pain, or warmth in an arm or leg.
  • Severe Skin Reaction: A widespread or peeling skin rash, blisters, or flu-like symptoms like high fever and joint pain.
  • Signs of Bleeding: Unexpected bruising, nosebleeds, bleeding gums, or blood in the stool or urine.
  • Signs of Infection: Fever (>38 C or 100.4 F), chills, or any signs of severe infection due to low blood cell counts.
  • Signs of Liver Problems (Hepatotoxicity): Yellowing of the skin or eyes (jaundice), dark urine, or pain in the upper right side of the abdomen.

Do not delay seeking help, as early intervention is essential for managing serious drug-related events.

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Therapeutic Uses of Revlimid 25mg

What Revlimid 25mg Treats: Main Uses and Benefits

The therapeutic profile of Lenalidomide (Revlimid) is commonly used in situations involving systemic malignant disorders of the blood and bone marrow.

The medication is utilized for several specific malignant conditions and may assist with managing their systemic impact and associated symptoms. These conditions include Multiple Myeloma, specific types of Non-Hodgkin Lymphoma (Mantle Cell, Follicular, and Marginal Zone Lymphoma), and Myelodysplastic Syndromes (MDS) presenting with a deletion 5q cytogenetic abnormality. This therapy is used to help with managing symptom patterns and contributes to easing the symptomatic burdens related to these conditions.

Maintenance and Control of Malignancy

Lenalidomide is often used as a maintenance treatment following procedures such as autologous stem cell transplant for Multiple Myeloma. This is commonly used to help with sustaining therapeutic responses achieved, contributing to easing the overall symptom load associated with progression or relapse. The application is relevant for easing symptoms of severe, chronic anemia that necessitates frequent red blood cell transfusions in eligible MDS patients. The treatment may assist with maintaining functional stability by reducing the need for regular transfusions, thereby helping to ease profound fatigue and supporting general well-being during symptomatic periods.


Quick Fact: Relief for Chronic Symptom Burden
Primary Focus: Managing systemic symptoms related to cancer activity and blood cell deficiencies.
Patient-oriented benefits: Supports the patient during difficult episodes by easing distress and assists with maintaining functional stability.
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Eligibility and Restrictions for Use

Eligibility Map: Who Can and Cannot Use Revlimid 25mg — Official Regulatory Information

Category Official Regulatory Statement
Populations for whom use is allowed (as stated in label): Adult patients across all approved indications.
Populations for whom use is not recommended (if applicable): Patients with Chronic Lymphocytic Leukemia (CLL) outside of controlled clinical trials.
Populations for whom use is contraindicated: Females who are pregnant (due to Embryo-Fetal Toxicity risk); Patients with demonstrated severe hypersensitivity to lenalidomide.
Age-related eligibility rules: Safety and effectiveness have not been established in pediatric patients (under 18 years of age). Use is established in older adults.
Condition-specific eligibility rules: Patients with moderate or severe renal impairment or who are on dialysis require an adjustment to the starting dose. Specific dose recommendations are not available for patients with severe hepatic impairment.
Pregnancy and lactation eligibility status (if explicitly documented): Pregnancy: Use is contraindicated; Lactation: Patients must not breastfeed during treatment.
Eligibility-related restrictions: Females of reproductive potential must comply with all requirements of the Pregnancy Prevention Programme. Males must use a condom; patients must not donate blood or sperm during treatment.

Eligibility Classifications (High-Level)

Category Classification Details (as defined in official documents)
Eligibility severity classification (as defined in official documents): Contraindicated (Pregnancy, Hypersensitivity); Not Recommended (CLL); Conditional Use (Renal Impairment, Reproductive Potential).
Regulatory basis (EMA / FDA / etc.): Restricted Distribution Program (REMS/PPP) due to Embryo-Fetal Toxicity.

Resulting Eligibility Structure

Official eligibility statements:

  • Use is contraindicated in females who are pregnant and in patients with a history of severe hypersensitivity to the drug.
  • The medicine is not recommended for the treatment of patients with Chronic Lymphocytic Leukemia (CLL) outside of controlled clinical trials.
  • Eligibility for females of reproductive potential is conditional upon strict adherence to the mandatory Pregnancy Prevention Programme requirements.
  • Use is established only for adult patients; safety and efficacy are not established in the pediatric population.
  • Regimens for patients with renal impairment must be adjusted based on the level of kidney function.

Connection to the overall eligibility profile:

The official regulatory documents define eligibility primarily through absolute contraindications related to pregnancy and hypersensitivity. Conditional eligibility is established through the mandatory restricted distribution program and specific requirements for renal function adjustment, ensuring the drug is only used in adult populations who meet strict reproductive and organ function criteria defined by the regulatory authorities.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

The official regulatory profile for Lenalidomide (Revlimid) defines documented interaction patterns based on both pharmacokinetic (PK) and pharmacodynamic (PD) mechanisms, focusing on additive risks and exposure modifications.


Pharmacodynamic Interactions (Additive Risks)

Co-administration with certain medicinal products is officially associated with an increased risk of specific events. The combination with Dexamethasone or Erythropoietin-Stimulating Agents (ESAs) contributes to an elevated risk of Venous Thromboembolic Events (VTE). This VTE risk is also increased when co-administered with estrogen-containing therapies, which includes combined oral contraceptives. Due to this risk, combined oral contraceptive pills are officially not recommended when Lenalidomide is used with Dexamethasone. Furthermore, combining Lenalidomide with agents like Clozapine may increase the risk of blood cell problems due to overlapping toxicity.


Pharmacokinetic and Metabolic Interactions

Lenalidomide is not classified as a clinically relevant inhibitor or inducer of major Cytochrome P450 (CYP) enzymes. However, a documented PK interaction exists with Digoxin, where co-administration officially increases the plasma concentration (Cmax and AUC) of Digoxin. Due to this effect, periodic monitoring of Digoxin plasma levels is formally required. The effect of Lenalidomide co-administration on Warfarin is officially stated to increase or decrease the Warfarin effect. The administration of Lenalidomide is not restricted by food intake as its absorption is not altered.

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Mechanism of Action

Lenalidomide (Revlimid) operates via a specific mechanism known as Targeted Protein Degradation (TPD), which involves reprogramming a cellular complex. ### Molecular Glue: Induced Destruction of Regulatory ProteinsLenalidomide functions as a "molecular glue" by binding directly to the protein Cereblon (CRBN), a component of the cell's natural disposal system (the E3 ubiquitin ligase complex). This binding event forces the recruitment and subsequent degradation of two key transcription factors, Ikaros (IKZF1) and Aiolos (IKZF3), which are critical regulators of lymphoid cell proliferation and survival. The resulting rapid clearance of IKZF1/3 initiates apoptosis (programmed cell death) and cell cycle arrest, resulting in a direct reduction in proliferation.### Immunomodulation and Systemic Immune FunctionThe degradation of IKZF1/3 simultaneously modulates the function of immune cells. By removing these transcriptional repressors, the drug promotes the activation and proliferation of cytotoxic immune cells, specifically T-cells and Natural Killer (NK) cells, while increasing their cytotoxic function against target cells. This modulation promotes the activity and expansion of T-cells and NK cells within the physiological system.### Disruption of Proliferation Support StructuresLenalidomide also exerts an inhibitory effect on the cellular microenvironment by suppressing the production of key mediators that support cell proliferation. It limits the synthesis of factors that trigger new blood vessel formation (anti-angiogenesis, via VEGF suppression) and reduces the levels of pro-inflammatory signals (like TNF-\alpha and IL-6). This action alters the supportive microenvironment by limiting factors necessary for cell proliferation and vascularization.

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Dosage and Administration Information

How to Use Revlimid 25mg — Administration Guidelines

Administration and Timing

Revlimid (lenalidomide) 25 mg capsules are taken by oral route, once daily, at approximately the same time each day. The capsule is to be swallowed whole with water and must not be opened, broken, or chewed. The medicine may be taken with or without food. If powder from a broken capsule contacts the skin, the area must be washed immediately with soap and water; if it contacts the eyes, nose, or mouth, the area must be flushed well with water.

Dosing Schedule and Cycles

The 25 mg dose is typically prescribed according to a 28-day cycle. For multiple myeloma combination therapy, the recommended starting dose is 25 mg once daily on Days 1 through 21 of each 28-day cycle, followed by a rest period on Days 22 through 28 where no dose is taken. This schedule continues until the healthcare provider determines a change is necessary based on clinical and laboratory findings.

Missed Dose and Dose Adjustment

  • Missed Dose: If a dose is missed, it should be taken only if it has been less than 12 hours since the regular scheduled time. If more than 12 hours have passed, the missed dose is skipped, and the next dose should be taken at the normal time. Do not take two doses at the same time to make up for a missed dose.
  • Dose Modification: Treatment is continued or modified by the prescriber based on specific patient factors, including laboratory test results (e.g., blood cell counts) or evidence of renal impairment. A lower starting dose is recommended for adult patients with moderate or severe renal impairment.
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Recent Clinical Evidence

Research evidence / Overview of studies for Revlimid 25mg

This overview summarizes the official research evidence for lenalidomide (Revlimid) to help contextualize the clinical evaluation of the medicine. It focuses on the structure of the studies, the outcomes they monitored, and areas where certainty remains low in the scientific literature.


Evidence for Use in Multiple Myeloma

The medicine was evaluated in large-scale Randomized Controlled Trials (RCTs) used in the core research for newly diagnosed multiple myeloma (NDMM) and as a maintenance therapy following stem cell transplant. Research examined time-related disease events, such as Progression-Free Survival (PFS) and Overall Survival (OS). Trials monitored measurements of the time before disease progression; the data showed patterns observed in the period before disease progression compared to control groups receiving similar regimens without the active substance. For maintenance, long-term follow-up data also described observations in the time to death compared to control groups. The ideal length of administration remains a focus of ongoing research.


Research in Myelodysplastic Syndromes (MDS)

Research has focused heavily on patients with a specific chromosomal abnormality known as deletion 5q. The studies conducted were primarily Phase 2 and Phase 3 multicenter studies. These trials was studied for patients who required frequent red blood cell transfusions. The primary outcome research examined was achieving and maintaining Red Blood Cell Transfusion Independence (TI). Pivotal trials described the proportion of patients monitored who met the measurement threshold for red blood cell transfusion requirements in the targeted deletion 5q population. Limited comparative evidence is lacking for patients presenting with the 5q deletion alongside multiple other cytogenetic abnormalities.


Studies in Select Non-Hodgkin Lymphoma Subtypes

Research examined conditions in the relapsed or refractory setting for certain types of Non-Hodgkin Lymphoma (NHL), including Mantle Cell Lymphoma (MCL) and certain indolent lymphomas. Study designs included both single-arm Phase 2 monotherapy studies and Phase 3 comparative trials using the medicine in combination with other agents. Outcomes research monitored included rates of tumor response and measures of disease control over time. Findings were mixed across different subtypes of lymphoma and depended on whether the medicine was used alone or in combination with other agents, which suggests data are heterogeneous.


Areas of Scientific Uncertainty and Evidence Gaps

Despite extensive research, scientific uncertainty remains. For instance, research provides context but not individual predictions, and long-term effects are not fully established for all possible patient profiles. Limited information for long-term outcomes exists regarding outcomes after a patient experiences disease progression while taking the medicine.

Key Studies & References

  1. Lenalidomide plus low-dose dexamethasone versus lenalidomide plus high-dose dexamethasone as initial treatment for newly diagnosed multiple myeloma: a randomized open-label phase III trial (MM-020/FIRST).
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Frequently Asked Questions (FAQ)

Common questions about Revlimid 25mg (FAQ)


Q: What is the difference between Revlimid and thalidomide?

Regulatory documents describe the active substance, lenalidomide, as an analogue or derivative of thalidomide. Both medicines belong to the same pharmacological class and are classified by official authorities as known human teratogens. This classification requires that both drugs be managed under strict, mandatory restricted distribution programs to prevent use during pregnancy.


Q: Is it true that Revlimid can increase the risk of blood clots?

Yes, official safety information classifies the risk of Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) as common serious vascular events. This risk is specifically documented as increased when lenalidomide is used in combination with another medicine, dexamethasone.


Q: Can taking Revlimid 25mg make me more susceptible to infections?

Regulatory documents list the risk of Serious Infections as a potential concern. The medicine is documented to frequently cause neutropenia, which is a decrease in white blood cells. This effect is what may lead to an increased susceptibility to infection, requiring blood count monitoring.


Q: Can Revlimid 25mg affect fertility in men or women?

Because the drug is strictly classified as a known human teratogen (risk of severe birth defects), strict reproductive constraints are necessary. Females of reproductive potential must participate in a mandatory Pregnancy Prevention Programme. For males, official guidelines require the use of a condom and prohibit sperm donation while on the drug.


Q: What kind of symptoms should I be aware of that require immediate attention while on Revlimid?

Regulatory documents describe symptoms that indicate the need for immediate medical attention, which relate to the documented serious risks. These symptoms may include signs of blood clots (such as chest pain, trouble breathing, or swelling in an arm or leg) and signs of severe liver problems (such as yellowing of the skin or eyes, or dark urine).


Q: Can Revlimid cause digestive issues like diarrhea or constipation?

Yes, official regulatory labeling classifies both diarrhea and constipation as very common adverse reactions. The frequency classification indicates these effects were commonly observed in clinical studies.


Q: Can elderly patients take the 25mg dose of Revlimid?

Use of the medicine is established in older adult populations. However, the drug is mainly cleared from the body by the kidneys. Due to this factor, official guidelines indicate that dose adjustments based on renal function are a necessary consideration in this patient group.


Q: How quickly does Revlimid 25mg start to work, or is it a long-term treatment?

Official guidelines state that treatment is generally continued until the disease is no longer being controlled or until side effects become unacceptable. Research studies supporting the use of the drug examine long-term results, such as the time until the disease progresses.


Q: Can Revlimid 25mg affect my sleep?

Official documents list insomnia, or difficulty sleeping, as a possible adverse reaction. Official product information notes that due to the potential for fatigue and drowsiness, caution is described regarding driving or operating machinery.


Q: Are there certain foods or drinks I should avoid while taking Revlimid 25mg?

According to the official administration guidelines, the medicine can be taken with or without food. No specific restrictions on foods or drinks are stated in the regulatory administration instructions.


Q: Does Revlimid 25mg interact with common over-the-counter pain relievers?

Official drug labels document that all medicines, including over-the-counter products, vitamins, and herbal supplements, should be reviewed by a healthcare provider. This is because these products may affect how the drug works or increase the risk of side effects.


Q: Why is Revlimid sometimes used in combination with another drug called dexamethasone?

The combination of lenalidomide with dexamethasone is an official, approved (indicated) treatment regimen for adult patients with multiple myeloma. This specific combination was the subject of the pivotal clinical research trials.


Q: Is fatigue a common experience for people taking Revlimid 25mg?

Yes, regulatory documents classify fatigue and asthenia (a lack of energy) as very common adverse reactions. The 'very common' classification indicates these effects were reported frequently in clinical studies.


Q: What kind of routine blood tests are typically required when a person is on Revlimid?

Regulatory documents require frequent monitoring of Complete Blood Counts (CBC). These tests check levels of blood cells, including white blood cells and platelets, particularly during the initial cycles of treatment, because the drug can cause decreases in these counts.


Q: How does Revlimid 25mg relate to the immune system?

Lenalidomide is classified as an immunomodulatory agent. This means its primary action is to modulate, or adjust, the function of the immune system. Official documents indicate it works by promoting the activity of certain immune cells, such as T-cells and Natural Killer (NK) cells.


Q: Is Revlimid used for any condition other than multiple myeloma?

Yes, the drug has approved (indicated) uses for other conditions. Official documents list its use for certain types of Myelodysplastic Syndromes (MDS) and certain subtypes of Non-Hodgkin Lymphoma (NHL).


Q: What is myelodysplastic syndrome (MDS) and how does Revlimid treat it?

The form of MDS for which the medicine is indicated involves a specific chromosome abnormality, often leading to low red blood cell counts and the need for frequent blood transfusions. The goal of treatment with lenalidomide is to help patients achieve red blood cell transfusion independence (TI), meaning fewer transfusions are needed.


Q: Are there warnings about driving or operating machinery while on Revlimid?

Official product information advises caution regarding driving or operating machines. This is because the medicine can potentially cause side effects like fatigue, dizziness, blurred vision, and somnolence (drowsiness).


Q: Does Revlimid interact with vitamins or herbal supplements?

Official drug labels document that all products, including vitamins and herbal supplements, should be reviewed by a healthcare provider for potential interaction. This is a standard measure because of the potential for any supplement to affect prescription medication.


Q: How long can a person safely stay on Revlimid treatment?

Treatment is generally continued until the disease progresses, side effects become unacceptable, or the prescriber determines a change is needed. Official research continues to study the ideal length of administration for different patient groups.


Q: What happens if a patient taking Revlimid 25mg develops a rash?

Rash is a documented adverse effect. Regulatory documents state that for a moderate-to-severe rash, the treatment interruption or discontinuation must be considered by the prescriber. Immediate stopping is recommended for serious dermatological reactions.


Q: Why is the drug Revlimid considered an immunomodulatory agent?

It is classified as an immunomodulatory agent because official documents show it has properties that affect the immune system. This includes promoting the activity of certain immune cells, such as T-cells and Natural Killer (NK) cells, while also reducing pro-inflammatory signals.


Q: Can Revlimid 25mg cause a tingling or numbness sensation (neuropathy)?

Yes, Peripheral Neuropathy is classified in regulatory documents as a common adverse reaction. Peripheral neuropathy is the clinical term for a sensation of tingling, numbness, or weakness, usually in the hands and feet.


Q: Are there any specific warnings for patients with a history of heart problems taking Revlimid?

Official information documents an increased risk of myocardial infarction (heart attack) and stroke, particularly when the drug is used with dexamethasone. The label also notes that severe adverse cardiovascular reactions, including cardiac failure, have occurred in some study populations.


Q: Can Revlimid affect my mood or cause anxiety?

Yes, adverse reactions documented in official sources include mood changes, anxiety, and depression. These are important effects to monitor and discuss with a healthcare provider.


Q: Is there a generic version of Revlimid 25mg available?

Information tracked by health agencies confirms that generic versions of the active substance, lenalidomide, have become available for distribution in the United States following the expiration of certain patent restrictions.


Q: How is Revlimid 25mg eliminated from the body?

Official regulatory documents state that the active substance, lenalidomide, is primarily excreted unchanged by the kidney. This is why monitoring of kidney function and dose adjustments are explicitly recommended for patients with reduced kidney function.


Q: Does alcohol consumption present a risk when taking Revlimid 25mg?

While there is no known direct interaction between the drug and alcohol, the official safety profile documents a risk of hepatotoxicity (liver damage). Due to the documented risk of liver damage (hepatotoxicity), reduced alcohol intake is often a general precaution discussed by healthcare providers.


Q: Is Revlimid a form of targeted therapy?

While the official class is immunomodulatory agent, the mechanism of action is highly specific. It operates via Targeted Protein Degradation (TPD), forcing the breakdown of specific proteins necessary for the survival of abnormal cells.


Q: What kind of severe skin reactions are described in official safety information for Revlimid?

Regulatory documents describe a risk of severe dermatologic reactions and Hypersensitivity Reactions. These include life-threatening conditions such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN).

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How should Revlimid 25mg be stored and disposed of?

Storage and Disposal Requirements

Revlimid (lenalidomide) 25 mg capsules must be stored and disposed of according to strict regulatory guidelines to maintain product integrity and prevent exposure.

Storage Conditions

Lenalidomide must be stored at room temperature, specifically between 20 C and 25 C (68 F to 77 F). The medicine must be kept in a tightly closed container, away from moisture, heat, and direct light, and should not be frozen.

Storage Requirement Rule
Temperature Range 20 C to 25 C (68 F to 77 F)
Security Must be kept out of the sight and reach of children and stored locked up.
Capsule Integrity Capsules must not be opened, broken, or chewed.

Disposal and Handling

Unused or expired Revlimid capsules must not be discarded in household waste or poured down the drain. The official regulatory instruction is to return unused product to a healthcare professional or pharmacist for proper disposal, in accordance with local hazardous waste regulations. Caregivers handling a damaged capsule should use disposable gloves, and pregnant women must not handle the product.

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

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