. If possible, complete all age-appropriate vaccinations at least 2 weeks prior to initiation of immunosuppressant therapy. Ask your pharmacist or doctor for a copy of the manufacturer's information for the patient. Modify Therapy/Monitor Closely. Either increases effects of the other by immunosuppressive effects; risk of infection. Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. Modify Therapy/Monitor Closely. Modify Therapy/Monitor Closely. Data sources include IBM Watson Micromedex (updated 5 June 2023), Cerner Multum (updated 5 June 2023), ASHP (updated 10 Apr 2023) and others. Either increases effects of the other by immunosuppressive effects; risk of infection. Either increases effects of the other by immunosuppressive effects; risk of infection. Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. Modify Therapy/Monitor Closely. after cessation of immunosuppressive therapy. Tablets only: Indicated for palliative treatment of patients with multiple myeloma (MM), After adequate recovery from toxicity (monitor WBCs and platelets) give 1-3 mg or 0.05 mg/kg PO qDay, Indicated for use as a high-dose conditioning treatment prior to hematopoietic progenitor (stem) cell transplantation in patients with MM, 100 mg/m/day IV administered over 30 min for 2 consecutive days (Day -3 and Day -2) prior to autologous stem cell transplantation (ASCT, Day 0), Patients weighing >130% of their ideal body weight, body surface area should be calculated based on adjusted ideal body weight, High dose conditioning treatment prior to hematopoietic progenitor (stem) cell transplantation, Orphan sponsor: CyDex Pharmaceuticals, Inc; 10513 W. 84th Terrace; Lenexa, KS 66214, Sponsor: Delcath Systems, Inc; 1301 Avenue of the Americas, 43rd Floor; New York, NY 10019, Sponsor: Icon Bioscience, Inc; 1253 Reamwood Ave; Sunnyvale, CA 94089, influenza virus vaccine quadrivalent, intranasal, measles, mumps, rubella and varicella vaccine, live, diphtheria & tetanus toxoids/ acellular pertussis vaccine, diphtheria & tetanus toxoids/acellular pertussis/poliovirus, inactivated vaccine, human papillomavirus vaccine, quadrivalent, influenza virus vaccine (H5N1), adjuvanted, influenza virus vaccine quadrivalent, adjuvanted, influenza virus vaccine quadrivalent, cell-cultured, influenza virus vaccine quadrivalent, recombinant, influenza virus vaccine trivalent, adjuvanted, influenza virus vaccine trivalent, recombinant, meningococcal A C Y and W-135 diphtheria conjugate vaccine, meningococcal A C Y and W-135 polysaccharide vaccine combined, tetanus & reduced diphtheria toxoids/ acellular pertussis vaccine, Females: Advise females of reproductive potential to use effective contraception during treatment and for 6 months after last dose, Males: Drug administration may damage spermatozoa and testicular tissue, resulting in possible genetic fetal abnormalities; advise males with female partners of reproductive potential to use effective contraception during treatment and for 3 months after last dose, Females: Therapy causes suppression of ovarian function in premenopausal women, resulting in amenorrhea in a significant number of patients, Males: Reversible and irreversible testicular suppression has been reported in male patients after administration of melphalan, In animal studies, melphalan was embryolethal and teratogenic in rats at doses below recommended clinical doses; advise a pregnant woman of potential risk to a fetus, Rapidly inject 10 mL of the supplied diluent directly into the vial containing lyophilized powder using a needle 20-gauge, Immediately shake vial vigorously until a clear solution is obtained, Dissolve powder initially with 10 mL of provided diluent to 5 mg/mL, Rapid addition of the diluent followed by immediate vigorous shaking is important for proper dissolution, Immediately dilute solution in 0.9% NaCl to concentration <0.45 mg/mL, Keep to a minimum (<60 min) time between reconstitution/dilution & administration, Do not refrigerate solution; precipitation occurs, Standard dilution: dose/250-500 mL 0.9% NaCl (concentration <0.45 mg/mL); must be prepared fresh, Captisol-enabled; propylene glycol-free product, Use 8.6 mL 0.9% NaCl to reconstitute vial contents (yields 50 mg/10 mL [5 mg/ mL] solution), The normal saline used to reconstitute each vial should appear to be assisted or pulled into the vial by the negative pressure (partial vacuum) present in the vial; discard any vial (and replace with another vial) if there is no vacuum present when reconstituting the vial with normal saline, Reconstituted solution is stable for 24 hr refrigerated (5C)without any precipitation due to the high solubility or for 1 hr at room temperature, Calculate the required volume of reconstituted solution needed for the dose and withdraw that volume from the vial(s), Add the required dosage volume to the appropriate volume of 0.9% NaCl to a final concentration of 0.45 mg/mL, Admixture solution is stable for 4 hr at room temperature in addition to the 1 hr following reconstitution, FDA approved for administration as a single infusion over a minimum of 15-20 min, Complete administration within 60 min of reconstituting the lyophilized powder, May be administered via central line and via peripheral vein as a rapid IV bolus, Central line: IV bolus doses of 17-200 mg/ reconstituted and not diluted) have been given over 2-20 min, Peripheral line: IV bolus doses of 2-23 mg/ reconstituted and not diluted) have been given over 1-4 min, Administer prophylactic antiemetic agents, Palliative: Infuse IV over 15-20 minutes via an injection port or central venous catheter, Conditioning: Infuse IV over 30 minutes via an injection port or central venous catheter. melphalan will increase the level or effect of tofacitinib by immunosuppressive effects; risk of infection. Monitor Closely (1)melphalan and isavuconazonium sulfate both decrease immunosuppressive effects; risk of infection. From April 1996 to January 2006 our acute myeloid leukemia treatment . after cessation of immunosuppressive therapy. . Your doctor will probably tell you not to take melphalan. after cessation of immunosuppressive therapy. If the victim has collapsed, had a seizure, has trouble breathing, or can't be awakened, immediately call emergency services at 911. Melphalan may increase the risk that you will develop other cancers. If possible, complete all age-appropriate vaccinations at least 2 weeks prior to initiation of immunosuppressant therapy. Monitor Closely (1)melphalan decreases effects of influenza virus vaccine quadrivalent, recombinant by pharmacodynamic antagonism. Avoid vaccination during chemotherapy or radiation therapy if possible because antibody response might be suboptimal. It is usually taken on an empty stomach once a day. Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. Avoid or Use Alternate Drug. Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. If possible, complete all age-appropriate vaccinations at least 2 weeks prior to initiation of immunosuppressant therapy. Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. melphalan decreases effects of haemophilus influenzae type b vaccine by pharmacodynamic antagonism. Applies only to oral form of both agents. This may cause certain symptoms and may increase the risk that you will develop a serious infection or bleeding. If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online (http://www.fda.gov/Safety/MedWatch) or by phone (1-800-332-1088). Other (see comment). Patients vaccinated within a 14-day period before starting or during immunosuppressive therapy should be revaccinated =3 months after therapy is discontinued if immune competence has been restored. Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. ofatumumab SC, melphalan. Monitor Closely (1)melphalan decreases effects of tetanus & reduced diphtheria toxoids/ acellular pertussis vaccine by pharmacodynamic antagonism. Monitor Closely (1)melphalan decreases effects of diphtheria & tetanus toxoids by pharmacodynamic antagonism. Talk with your doctor about the risks of taking melphalan. Melphalan may cause other side effects. Melphalan is also used to treat a certain type of ovarian cancer (cancer that begins in the female reproductive organs where eggs are formed). Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. Talk to your doctor about how you are feeling during your treatment. Adding plans allows you to compare formulary status to other drugs in the same class. Avoid or Use Alternate Drug. Either increases toxicity of the other by pharmacodynamic synergism. . Neutropenia or febrile neutropenia incidence were increased when trastuzumab was coadministered with myelosuppressive chemotherapy. melphalan, denosumab. Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. Dosage is adjusted to between 1 and 3 mg/day depending on the hematological response. Live-attenuated vaccines should be avoided for at least 3 mo. NOTES: Do not share this medication with others.Lab and/or medical tests (such as complete blood count, liver function) should be done while you are taking this medication. It is important to keep all medication out of sight and reach of children as many containers (such as weekly pill minders and those for eye drops, creams, patches, and inhalers) are not child-resistant and young children can open them easily. Minor/Significance Unknown. Monitor Closely (1)melphalan decreases effects of influenza virus vaccine (H5N1), adjuvanted by pharmacodynamic antagonism. Consult your pharmacist or local waste disposal company. Live-attenuated vaccines should be avoided for at least 3 mo. Use Caution/Monitor. If possible, complete all age-appropriate vaccinations at least 2 weeks prior to initiation of immunosuppressant therapy. . Patients should be informed that the major toxicities of this drug are related to bone marrow suppression, hypersensitivity reactions, GI toxicity, and pulmonary toxicity. Serious - Use Alternative (1)ropeginterferon alfa 2b, melphalan. Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. informational and educational purposes only. If possible, complete all age-appropriate vaccinations at least 2 weeks prior to initiation of immunosuppressant therapy. after cessation of immunosuppressive therapy. The current match involves a Texas lawsuit . Monitor Closely (2)melphalan decreases effects of sipuleucel-T by immunosuppressive effects; risk of infection. melphalan decreases effects of influenza virus vaccine trivalent by pharmacodynamic antagonism. . Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. Immunosuppressives may diminish therapeutic effects of vaccines and increase risk of adverse effects (increased risk of infection). . Sildenafil, a phosphodiesterase-5 (PDE-5) inhibitor, is the active ingredient in a tablet for oral administration currently marketed under the brand name Viagra for the treatment of ED in men. . Coadministration with immunosuppressant therapy reduced efficacy of the vaccine may occur. Do not start, stop, or change the dosage of any medicines without your doctor's approval. Graham Head, 66, who kidnapped and tried to rape two women, was caught after one victim remembered three digits of his car registration. Unless otherwise directed by your doctor, drink plenty of fluids to help prevent side effects.The dosage and treatment schedule are based on your medical condition and response to treatment. There is no specific information comparing the use of melphalan in the elderly with use in other age groups. Use Caution/Monitor. However, get medical help right away if you notice any symptoms of a serious allergic reaction, such as: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.This is not a complete list of possible side effects. melphalan decreases effects of poliovirus vaccine inactivated by pharmacodynamic antagonism. Immunosuppressives may diminish therapeutic effects of vaccines and increase risk of adverse effects (increased risk of infection). You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. Use caution when switching patients from long-acting therapies with immune effects. Comment: Palifermin should not be administered within 24 hrbefore, during infusion of, or within 24 hr after administration of antineoplastic agents. Patients vaccinated <14 days before initiation or during immunosuppressive therapy should be revaccinated at least 3 months after therapy is discontinued. AHFS Patient Medication Information. Consider not using a leflunomide loading dose in patients receiving other immunosuppressants. Get emergency medical help if you have signs of an allergic reaction: hives, itching, skin redness; blurred vision, feeling light-headed; fast heartbeats; trouble breathing; swelling of your face, lips, tongue, or throat.. Melphalan may cause serious side effects. The racemic (DL-) form is known as merphalan or sarcolysin. Immunosuppressives may diminish therapeutic effects of vaccines and increase risk of adverse effects (increased risk of infection). Serious - Use Alternative (1)melphalan, lisocabtagene maraleucel. Contraindicated (1)melphalan decreases effects of measles, mumps, rubella and varicella vaccine, live by pharmacodynamic antagonism. vitamin A, melphalan. melphalan will decrease the level or effect of digoxin by Other (see comment). . Contraindicated. Other (see comment). 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