THALOMID® (thalidomide) in combination with dexamethasone is indicated for the treatment of patients with newly diagnosed multiple myeloma (MM).
THALOMID is indicated for the acute treatment of the cutaneous manifestations of moderate to severe erythema nodosum leprosum (ENL).
THALOMID is not indicated as monotherapy for such ENL treatment in the presence of moderate to severe neuritis. THALOMID is also indicated as maintenance therapy for prevention and suppression of the cutaneous manifestations of ENL recurrence.
IMPORTANT SAFETY INFORMATION
WARNING: EMBRYO-FETAL TOXICITY and VENOUS THROMBOEMBOLISM
If THALOMID (thalidomide) is taken during pregnancy, it can cause severe birth defects or embryo-fetal death. THALOMID should never be used by females who are pregnant or who could become pregnant while taking the drug. Even a single dose [1 capsule (regardless of strength)] taken by a pregnant woman during her pregnancy can cause severe birth defects.
Because of this toxicity and in an effort to make the chance of embryo-fetal exposure to THALOMID as negligible as possible, THALOMID is approved for marketing only through a special restricted distribution program: THALOMID REMS® program, approved by the Food and Drug Administration.
You can get the information about THALOMID and the THALOMID REMS® program on the Internet at www.celgeneriskmanagement.com or by calling the manufacturer’s toll-free number 1-888-423-5436.
The use of THALOMID in multiple myeloma results in an increased risk of venous thromboembolism, such as deep venous thrombosis and pulmonary embolism. This risk increases significantly when THALOMID is used in combination with standard chemotherapeutic agents including dexamethasone. In one controlled trial, the rate of venous thromboembolism was 22.5% in patients receiving THALOMID in combination with dexamethasone compared to 4.9% in patients receiving dexamethasone alone (p = 0.002). Patients and physicians are advised to be observant for the signs and symptoms of thromboembolism. Instruct patients to seek medical care if they develop symptoms such as shortness of breath, chest pain, or arm or leg swelling. Consider thromboprophylaxis based on an assessment of individual patients’ underlying risk factors.
Pregnancy: See Boxed WARNINGS: THALOMID is contraindicated in females who are pregnant. THALOMID can cause fetal harm when administered to a pregnant female. THALOMID is a powerful human teratogen, inducing a high frequency of severe and life-threatening birth defects, even after a single dose. Mortality at or shortly after birth has been reported in about 40% of infants. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential risk to the fetus. If pregnancy occurs during THALOMID treatment, the drug should be discontinued immediately.
Hypersensitivity: THALOMID is contraindicated in patients who have demonstrated hypersensitivity to the drug or its components.
WARNINGS AND PRECAUTIONS
Embryo-Fetal Toxicity: See Boxed WARNINGS
- Females of Reproductive Potential: Females of reproductive potential must avoid pregnancy for at least 4 weeks before beginning THALOMID therapy, during therapy, during dose interruptions and for at least 4 weeks after completing therapy. Females must commit either to abstain continuously from heterosexual sexual intercourse or to use two methods of reliable birth control, beginning 4 weeks prior to initiating treatment with THALOMID, during therapy, during dose interruptions and continuing for 4 weeks following discontinuation of THALOMID therapy.
- Males: Thalidomide is present in the semen of patients receiving the drug. Therefore, males must always use a latex or synthetic condom during any sexual contact with females of reproductive potential while taking THALOMID and for up to 4 weeks after discontinuing THALOMID, even if they have undergone a successful vasectomy. Male patients taking THALOMID must not donate sperm.
- Blood Donation: Patients must not donate blood during treatment with THALOMID and for 4 weeks following discontinuation of the drug because the blood might be given to a pregnant female patient whose fetus must not be exposed to THALOMID.
THALOMID REMS® Program: See Boxed WARNINGS: Because of the embryo-fetal risk, THALOMID is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS), the THALOMID REMS program. Prescribers and pharmacies must be certified with the program; and patients must sign an agreement form and comply with the requirements. Further information about the THALOMID REMS® program is available at www.celgeneriskmanagement.com or by telephone at 1-888-423-5436
Venous and Arterial Thromboembolism: The use of THALOMID in patients with MM results in an increased risk of venous thromboembolism, such as deep venous thrombosis and pulmonary embolism. This risk increases significantly when THALOMID is used in combination with standard chemotherapeutic agents including dexamethasone. In one controlled trial, the rate of venous thromboembolism was 22.5% in patients receiving THALOMID in combination with dexamethasone compared to 4.9% in patients receiving dexamethasone alone (p=0.002). Ischemic heart disease (11.1%), including myocardial infarction (1.3%), and stroke (cerebrovascular accident, 2.6%) have also occurred in patients with previously untreated MM treated with THALOMID and dexamethasone compared to placebo and dexamethasone (4.7%, 1.7%, and 0.9%, respectively) in one clinical trial. Consider thromboprophylaxis based on an assessment of individual patients’ underlying risk factors. Advise patients to seek immediate medical care if they develop symptoms such as shortness of breath, chest pain, or arm or leg swelling. Agents that may increase the risk of thromboembolism should be used with caution in patients receiving THALOMID.
Increased Mortality With Pembrolizumab: In two randomized clinical trials in patients with MM, the addition of pembrolizumab to a thalidomide analogue plus dexamethasone, a use for which no PD-1 or PD-L1 blocking antibody is indicated, resulted in increased mortality. Treatment of patients with MM with a PD-1 or PD-L1 blocking antibody in combination with a thalidomide analogue plus dexamethasone is not recommended outside of controlled clinical trials.
Drowsiness and Somnolence: THALOMID frequently causes drowsiness and somnolence. Patients should be instructed to avoid situations where drowsiness may be a problem and not to take other medications that may cause drowsiness without adequate medical advice. Dose reductions may be required.
Peripheral Neuropathy: THALOMID is known to cause nerve damage that may be permanent. Peripheral neuropathy is a common (≥10%) and potentially severe adverse reaction of treatment with THALOMID that may be irreversible.
Dizziness and Orthostatic Hypotension: Patients should be advised that THALOMID may cause dizziness and orthostatic hypotension and that, therefore, they should sit upright for a few minutes prior to standing up from a recumbent position.
Neutropenia: Decreased white blood cell counts, including neutropenia, have been reported in association with the clinical use of THALOMID. Treatment should not be initiated with an absolute neutrophil count (ANC) of <750/mm3. White blood cell count and differential should be monitored on an ongoing basis, especially in patients who may be more prone to neutropenia, such as patients who are HIV‑seropositive. If ANC decreases to below 750/mm3 while on treatment, the patient’s medication regimen should be re-evaluated and, if the neutropenia persists, consideration should be given to withholding THALOMID if clinically appropriate.
Thrombocytopenia: Thrombocytopenia, including Grade 3 or 4 occurrences, has been reported with the clinical use of THALOMID. Monitor blood counts, including platelet counts. Dose reduction, delay or discontinuation may be required. Monitor for signs and symptoms of bleeding including petechiae, epistaxis, and gastrointestinal bleeding, especially if concomitant medication may increase risk of bleeding.
Increased HIV Viral Load: In a randomized, placebo-controlled trial of THALOMID in an HIV‑seropositive patient population, plasma HIV RNA levels were found to increase (median change = 0.42 log10 copies HIV RNA/mL, p=0.04 compared to placebo). A similar trend was observed in a second, unpublished study conducted in patients who were HIV‑seropositive. The clinical significance of this increase is unknown.
Bradycardia: Bradycardia in association with THALOMID use has been reported. Monitor patients for bradycardia and syncope. Dose reduction or discontinuation may be required. Medications known to decrease heart rate should be used with caution in patients receiving THALOMID.
Severe Cutaneous Reactions: Severe cutaneous reactions including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reaction with eosinophilia and systemic symptoms (DRESS) have been reported with THALOMID use. DRESS may present with a cutaneous reaction (such as rash or exfoliative dermatitis), eosinophilia, fever, and/or lymphadenopathy with systemic complications such as hepatitis, nephritis, pneumonitis, myocarditis, and/or pericarditis. These events can be fatal. THALOMID interruption or discontinuation should be considered for Grade 2-3 skin rash. Discontinue THALOMID for Grade 4 rash, exfoliative or bullous rash, or for other severe cutaneous reactions such as SJS, TEN, or DRESS, and do not resume therapy.
Seizures: Although not reported from pre-marketing clinical trials, seizures, including grand mal convulsions, have been reported during post-approval use of THALOMID in clinical practice. Patients with a history of seizures or with other risk factors for the development of seizures should be monitored closely.
Tumor Lysis Syndrome: Monitor patients at risk of tumor lysis syndrome (e.g., patients with high tumor burden prior to treatment) and take appropriate precautions.
Contraceptive Risks: Some contraceptive methods may pose a higher risk of adverse effects or may be medically contraindicated in some patients treated with THALOMID. Because some patients may develop sudden, severe neutropenia and/or thrombocytopenia, use of an intrauterine device (IUD) or implantable contraception in these patients may carry an increased risk for infection or bleeding either at insertion, removal or during use. Treatment with THALOMID, the presence of an underlying malignancy, and/or use of an estrogen-containing contraceptive can each increase the risk of thromboembolism. It is not known if these risks of thromboembolism are additive. However, they should be taken into consideration when choosing contraceptive methods.
Hypersensitivity: Hypersensitivity, including angioedema and anaphylactic reactions to THALOMID has been reported. Signs and symptoms have included the occurrence of erythematous macular rash, possibly associated with fever, tachycardia, and hypotension, and if severe, may necessitate interruption of therapy. If the reactions recurs when dosing is resumed, THALOMID should be discontinued. Do not resume THALOMID treatment after angioedema and anaphylaxis.
- The safety analysis in Study 1 was conducted on 204 patients who received treatment. The most frequently reported adverse reactions (all grades) in multiple myeloma patients (occurring in ≥20% of patients treated with THALOMID/
dexamethasone compared with dexamethasone alone) in Study 1 were: fatigue (79% vs 71%), hypocalcemia (72% vs 59%), edema (56% vs 46%), constipation (55% vs 28%), neuropathy-sensory (54% vs 28%), dyspnea (42% vs 31%), muscle weakness (40% vs 37%), leukocytes (decreased) (35% vs 29%), neutrophils (decreased) (31% vs 24%), rash/desquamation (30% vs 18%), confusion (28% vs 12%), anorexia (28% vs 24%), nausea (28% vs 22%), anxiety/agitation (26% vs 14%), tremor (26% vs 6%), fever (24% vs 20%), thrombosis/embolism (22% vs 5%), weight loss (23% vs 21%), neuropathy-motor (22% vs 16%), weight gain (22% vs 13%), dry skin (21% vs 11%), and dizziness/lightheadedness (20% vs 14%).
- The most frequently reported Grade 3/4 adverse drug reactions occurring in ≥ 10% of patients treated with THALOMID/
dexamethasone compared with dexamethasone alone) in Study 1 were: fatigue (17% vs 13%), hypocalcemia (11% vs 5%), dyspnea (13% vs 15%), neutrophils (decreased) (10% vs 10%), thrombosis/embolism (21% vs 5%).
- Twenty-three percent of patients (47/204) discontinued due to adverse reactions; 30% (31/102) from the THALOMID/
dexamethasone arm and 16% (16/102) from the dexamethasone alone arm.
- The safety analysis in Study 2 was conducted on 466 patients who received treatment. The most common adverse drug reactions (all grades) reported in (≥ 20%) patients treated with THALOMID/
dexamethasone were constipation (50% vs 21%), peripheral edema (34% vs 25%), tremor (26% vs 12%), asthenia (24% vs 20%), dizziness (23% vs 14%) and fatigue (21% vs 16%).
- The most frequently reported Grade 3/4 adverse drug reactions occurring in > 5% of patients treated with THALOMID/
dexamethasone compared with dexamethasone alone) in Study 2 were: deep vein thrombosis (12% vs 2%), pulmonary embolism (7% vs 2%), pneumonia NOS (7% vs 6%), asthenia (5% vs 2%) and atrial fibrillation (5% vs 3%).
- Twenty-six percent of patients (121/466) discontinued due to adverse events; 37% (86/234) from the THALOMID/
dexamethasone arm and 15% (35/232) from the placebo/
Erythema Nodosum Leprosum
- Common adverse events, greater than or equal to 8%, reported in THALOMID treated patients in controlled clinical trials in ENL: somnolence (38%), rash (21%), headache (13%), asthenia (8%), malaise (8%), pain (8%), vertigo (8%), pruritus (8%), and impotence (8%).
Thalidomide is not a substrate of the cytochrome P450 system. At therapeutic concentrations, thalidomide is not an inhibitor or inducer of human cytochrome P450 enzymes in vitro. Pharmacokinetic drug-drug interactions with substrates, inhibitors or inducers of CYP450 are not anticipated.
The use of opioids, antihistamines, antipsychotics, anti-anxiety agents, or other CNS depressants concomitantly with THALOMID may cause an additive sedative effect and should be avoided.
Drugs which cause bradycardia or peripheral neuropathy may cause additive effects and should be used with caution.
Hormonal contraceptives increase the risk of thromboembolism.
In 13 healthy men, the pharmacokinetic profile and international normalized ratio (INR) of prothrombin time for warfarin, following a single oral dose of 25 mg, were similar with and without the coadministration of THALOMID 200 mg/day at steady-state levels. The single dose of warfarin had no effect on the pharmacokinetic profile of THALOMID
Concomitant use of HIV‑protease inhibitors, griseofulvin, modafinil, penicillins, rifampin, rifabutin, phenytoin, carbamazepine, or certain herbal supplements such as St. John’s Wort with hormonal contraceptive agents may reduce the effectiveness of the contraception up to one month after discontinuation of these concomitant therapies.
Erythropoietic agents, or other agents that may increase the risk of thromboembolism, such as estrogen containing therapies, should be used with caution in MM patients receiving THALOMID with dexamethasone.
USE IN SPECIFIC POPULATIONS
Pregnancy: See Boxed WARNINGS. If pregnancy does occur during treatment, immediately discontinue the drug, and refer the patient to an obstetrician/gynecologist experienced in reproductive toxicity for further evaluation and counseling. Report any suspected fetal exposure to THALOMID to the FDA via the MedWatch program at 1‑800‑332‑1088 and also to Celgene Corporation at 1‑888‑423‑5436. There is a pregnancy exposure registry that monitors pregnancy outcomes in females exposed to THALOMID during pregnancy as well as female partners of male patients who are exposed to THALOMID. This registry is also used to understand the root cause for the pregnancy
Lactation: There is no information regarding the presence of thalidomide in human milk, the effects of THALOMID on the breastfed infant, or the effects of THALOMID on milk production. Thalidomide is excreted in the milk of lactating rabbits. Because many drugs are excreted in human milk and because of the potential for adverse reactions in breastfed infants from THALOMID, advise female patients not to breastfeed during treatment with THALOMID
Pediatric Use: Safety and effectiveness in pediatric patients below the age of 12 years have not been established
Renal and Hepatic Impairment: No clinical studies were conducted with THALOMID in patients with mild, moderate, or severe renal function or with hepatic impairment
Please see U.S. Full Prescribing Information for THALOMID, including Boxed WARNINGS.
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