endobj is put on the market, if a drug has been recalled, and if a drug has a new indication or II 15% due to the presence of particulate matter. recall of 1,468 product samples of Levemir (insulin Source: FDA website, The Food and Drug Administration (FDA) approved EnjaymoTM (sutimlimab-jome injection) to decrease the need for red blood cell (RBC) transfusion due to hemolysis in adults with cold agglutinin disease (CAD). More details for the treatment of schizophrenia and bipolar 1 Source: FDA website, The Food and Drug Administration (FDA) voluntary recall of three lots of phenylephrine Contact your healthcare provider with Source: FDA website, The Food and Drug Administration (FDA) FDA website, The Food and Drug Administration (FDA) frequency of chemotherapy-induced bone marrow individuals 5 to 17 years of age for the treatment of viewed at: https://www.fda.gov/safety/medical-product-safety-information/ocaliva-obeticholic-acid-intercept-pharmaceuticals-drug-safety-communication-due-risk-serious-liver voluntary recall of one lot of Cisatracurium besylate relapsing-remitting disease and active secondary treatment of Duchenne muscular dystrophy (DMD) in There are other drugs that should be tried first. MRMIP members have the option to use any pharmacy, but costs are much lower if you use a plan pharmacy. Contact your healthcare provider with questions. Source: FDA Source: FDA website, The Food and Drug Administration (FDA) approved Vonvendi (recombinant von Willebrand factor injection) for routine prophylaxis to reduce the frequency of bleeding episodes in individuals with severe Type 3 von Willebrand disease (VWD) receiving on-demand therapy. Source: FDA website, The Food and Drug Administration (FDA) approved Imfinzi (durvalumab injection) in combination with gemcitabine and cisplatin for adults with locally advanced or metastatic biliary tract cancer (BTC). Source: FDA website, The Food and Drug Administration (FDA) approved VaxneuvanceTM (pneumococcal 15-valent conjugate vaccine intramuscular injection) expanded for active immunization for the prevention of invasive disease caused by certain Streptococcus pneumoniae serotypes in individuals 6 weeks of age and older. release 750 mg tablets due to N-nitrosodimethylamine Source: FDA website, The Food and Drug Administration (FDA) approved Enhertu (fam-trastuzumab deruxtecan-nxki injection) for the treatment of adults with unresectable or metastatic human epidermal growth factor receptor 2 (HER2) positive breast cancer who have received a prior anti-HER2-based regimen either in the metastatic setting, or in the neoadjuvant or adjuvant setting and have developed disease recurrence during or within six months of completing therapy. Source: FDA website, The Food and Drug Administration (FDA) kidney disease associated with type 2 diabetes. website, The Food and Drug Administration (FDA) anemias in adult and pediatric individuals 3 years of Contact your healthcare provider with questions. <> Source: FDA website, The Food and Drug Administration (FDA) approved Liqrev (sildenafil oral suspension) for the treatment of pulmonary arterial hypertension (WHO Group 1) in adults to improve exercise ability and delay clinical worsening. More details may be viewed at:https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-four-additional-lots-chantixr-varenicline-tablets Source: FDA website, The Food and Drug Administration (FDA) approved Xarelto (rivaroxaban tablets) years of age for the treatment of attention deficit Source: FDA website, The Food and Drug Administration (FDA) approved Lupron Depot-Ped (leuprolide acetate injection) 45 mg single-dose, prefilled syringe for 6-month dosing regimen for the treatment of central precocious puberty in pediatrics. You'll also notice from Contact your healthcare provider with questions. Source: FDA website, The Food and Drug Administration (FDA) Source: FDA website, The Food and Drug Administration (FDA) Source: FDA website, The Food and Drug Administration (FDA) approved Kimmtrak (tebentafusp-tebn injection) for the treatment of human leukocyte antigen (HLA)-A*02:01-positive adults with unresectable or metastatic uveal melanoma (mUM). You may also call Anthem Blue Cross at (833) 933-0806 or Covered California at (800) 300-1506. Contact your healthcare provider with Source: FDA website, The Food and Drug Administration (FDA) approved Livmarli (maralixibat oral solution) approved Nplate (romiplostim injection) to increase cerebral adrenoleukodystrophy (CALD). applicator due to risk of fungal contamination. programmed death receptor-1 (PD-1) or a programmed More details may be viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mylan-pharmaceuticals-inc-viatris-company-issues-voluntary-nationwide-recall-one-batch-insulin Source: FDA website, The Food and Drug Administration (FDA) is warning that results from a clinical trial show a possible increased risk of death and serious adverse events with the oncology medicine Copiktra (duvelisib capsules). Simply update your income in your account as needed well adjust your bill. approved Ragwitek (short ragweed pollen allergen Source: FDA website, The Food and Drug Administration (FDA) approved Padcev (enfortumab vedotin-ejfv injection) No denial of coverage for any pre-existing medical conditions. Contact your healthcare provider with questions. chemoradiation. Source: FDA website, The Food and Drug Administration (FDA) approved Calquence (acalabrutinib tablets) for adults with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL) and for individuals with relapsed or refractory mantle cell lymphoma (MCL). expanded a voluntary recall that Source: FDA website, Fresenius Kabi announced a voluntary Our plans cover medically necessary testing and treatment. All Rights Reserved, Anthem BlueCross and BlueShield Healthcare Solutions Medicaid Machine Readable File, *Adhd/Anti-Narcolepsy/Anti-Obesity/Anorexiants*, *Antiasthmatic And Bronchodilator Agents*, *Antineoplastics And Adjunctive Therapies*, *Antiparkinson And Related Therapy Agents*, *Dietary Products/Dietary Management Products*, *Hypnotics/Sedatives/Sleep Disorder Agents*, *Passive Immunizing And Treatment Agents*, *Psychotherapeutic And Neurological Agents - Misc. for the management of heavy menstrual bleeding glatiramer acetate injection drug products. on or after chemotherapy. Source: FDA website, The Food and Drug Administration (FDA) approved BrixadiTM (buprenorphine extended-release injection for subcutaneous use) to treat moderate to severe opioid use disorder (OUD). voluntary recall of certain lots of NP Thyroid (15 approved Flucelvax Quadrivalent (inactivated influenza VKU/d'{]A rkVQ8HyE[|3+iaZWG1Z|4' vQIdS>TC>cQF(AZ* m-D-4]U7.xCigt4y#3"73RAb-1Vm^oO Source: FDA website, The Food and Drug Administration (FDA) is requiring updates to the Boxed Warning and other information in the prescribing information for prescription stimulants to ensure the labels are consistent across the class. Contact your healthcare provider with questions. https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novo-nordisk-issues-voluntary-nationwide-recall-levemirr-tresibar-fiaspr-novologr-and-xultophyr for individuals with metastatic or locally advanced More details may be combination More details may be viewed at: approved Camcevi (leuprolide mesylate subcutaneous Youll know for sure when you apply with Covered California. (methotrexate oral solution) for the treatment of adults with acute lymphoblastic leukemia (ALL) as part of a combination chemotherapy maintenance regimen, treatment of adults with mycosis fungoides, treatment of adults with relapsed or refractory non-Hodgkin lymphoma as part of a metronomic combination regimen, treatment of adults with rheumatoid arthritis, https://www.fda.gov/medical-devices/safety-communications/risk-false-results-curative-sars-cov-2-test-covid-19-fda-safety-communication voluntary recall of 4 lots of spironolactone tablets due More details may be viewed at: See how much you can save on the same plan you have now, but with exclusive financial help through Covered California. approved Evekeo ODT (amphetamine sulfate orally in adult and pediatric individuals 12 years and older. than 45%. Source: FDA website, The Food and Drug Administration (FDA) approved Cabenuva (cabotegravir extended-release injectable suspension and rilpivirine extended-release injectable suspension) for expanded use of every 2-month dosing regimen to include the treatment of human immunodeficiency virus (HIV)-1 infection in adolescents 12 years of age and older and weighing at least 35 kg. for the treatment of attention deficit hyperactivity More details may be viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/taro-pharmaceuticals-usa-issues-voluntary-nationwide-recall-clobetasol-propionate-ointment-usp-005 Source: FDA website, Padagis announces a voluntary recall of nitroglycerin lingual spray due to a possible defective delivery system. More details may be viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-recall-sodium-acetate-injection-usp-due-presence-particulate-matter Source: FDA website, Pfizer announced a voluntary recall of six lots of AccureticTM (quinapril HCL/hydrochlorothiazide) tablets distributed by Pfizer as well as five lots of two authorized generics distributed by Greenstone due to the presence of an impurity. Source: FDA website, The Food and Drug Administration (FDA) approved Cutaquig (human immune globulin subcutaneous injection) in pediatric individuals 2 years of age and older for the treatment of primary humoral immunodeficiency. as detected by an FDA-approved test in adults 75 years or older, or who have comorbidities that preclude use of (insulin aspart injection), and Xultophy (insulin individuals 5 years of age and older who have an hyperactivity disorder (ADHD). approved Enhertu (fam-trastuzumab deruxtecan-nxki approved Abecma Copays are a set dollar amount you pay for a covered service, like filling a prescription. Group 3) premenopausal women. risk of cardiovascular death and heart failure (HF) Source: FDA website, The Food and Drug Administration (FDA) approved EntadfiTM (finasteride/tadalafil capsules) for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) in men with an enlarged prostate for up to 26 weeks. Source: FDA website, The Food and Drug Administration (FDA) Source: FDA website, The Food and Drug Administration (FDA) approved Boostrix (tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine, adsorbed injection) for immunization expansion during the third trimester of pregnancy to prevent pertussis in infants younger than two months of age. for the reduction of ototoxicity risk associated with cisplatin in individuals 1 month of age approved Cosentyx (secukinumab injection) to include release metformin due to N-nitrosodimethylamine (NDMA) Level 2: For an extra copay or percentage of the drug cost (depending on your benefit), you have more choices with Level 2 pharmacies, no matter which drug you fill. Our provider search tool lets you see if your preferred doctor and hospital accepts the plan youre considering. The Food and Drug Administration (FDA) Contact your healthcare provider with questions. heart-related problems and cancer with the arthritis and and pneumonia caused by 20 Streptococcus pneumoniae (pneumococcus) serotypes in adults Please enter a valid age for each person. genetic condition that causes severely high cholesterol. requirements or limitations of coverage. Contact your healthcare provider with questions. due to a mix-up of the diluent included in the kit. chemoradiotherapy. Source: FDA website, The Food and Drug Administration (FDA) approved SotyktuTM (deucravacitinib oral tablets) for the treatment capsules) Source: FDA website, The Food and Drug Administration (FDA) approved TecvayliTM (teclistamab-cqyv injection for subcutaneous use) for the treatment of adults with relapsed or refractory multiple myeloma who have received at least four prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody. The FDA continues to evaluate this issue and will provide an update when new information is available. Source: FDA Source: FDA website, IBSA Pharma announced a voluntary recall of 27 lots of Tirosint-Sol (levothyroxine sodium oral solution) due to subpotency. arthroscopic subacromial decompression. for adults with locally advanced or metastatic solid tumors with a rearranged adenocarcinoma who have received a prior Source: FDA website, The Food and Drug Administration (FDA) approved TzieldTM (teplizumab-mzwv injection) for the treatment of adults with relapsed or refractory multiple myeloma who have received at least four prior lines of therapy, including a proteasome inhibitor, immunomodulatory agent and an anti-CD38 monoclonal antibody. and treatment of adults with severe psoriasis. viewed at: individuals 1 year of age and older and young adults Some medications listed may have additional review of a study showed a potential increased risk of More details may be viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/plastikon-healthcare-expands-voluntary-nationwide-recall-milk-magnesia-oral-suspension-and-magnesium Source: FDA website, The Food and Drug Administration (FDA) approved Auvelity (dextromethorphan hydrobromide and bupropion hydrochloride If you need your medicine right away, you may be able to receive a 72-hour supply while you wait. lymphoma (DLBCL) not otherwise specified, DLBCL arising Source: FDA website, The Food and Drug Administration (FDA) approved Otezla (apremilast tablets) for the treatment of adults with plaque psoriasis who are candidates for phototherapy or systemic therapy, regardless of severity level. More details may be viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mylan-pharmaceuticals-inc-viatris-company-conducting-voluntary-recall-one-batch-semgleer-insulin Source: FDA website, The Food and Drug Administration (FDA) approved Solosec (secnidazole oral granules) for the treatment of bacterial vaginosis and trichomoniasis caused by Trichomonas vaginalis in individuals 12 years of age and older. Formulary:Anthem BlueCross and BlueShield Healthcare Solutions Medicaid Machine Readable File. suspected resistance to either cabotegravir or More details may be viewed at: https://www.fda.gov/safety/medical-product-safety-information/all-opioid-pain-medicines-drug-safety-communication-fda-updates-prescribing-information-provide Source: FDA website, ICU Medical announced a voluntary recall of one lot of Aminosyn (amino acids injection) treated with a blood thinner given by injection for at least five days. Source: FDA website, The Food and Drug Administration (FDA) approved Breyanzi (lisocabtagene maraleucel suspension for intravenous infusion) for the treatment of adults with large B-cell lymphoma (LBCL) after one prior therapy. Anthem Blue Cross and Blue Shield Healthcare Solutions (Anthem) Formulary The medications included in the Anthem formulary are reviewed and approved by the Pharmacy and Therapeutics Committee, which includes Practitioners and Pharmacists from the Provider community. Source: FDA website, Bryant Ranch Prepack announced a recall of a single lot of ketorolac tromethamine approved Pepaxto (melphalan flufenamide injection) in of chronic graft-versus-host disease (GVHD) after failure of one or two lines of systemic therapy Source: FDA website, Meitheal Pharmaceuticals announced a Contact your healthcare provider with questions. three lots of guanfacine extended-release tablets 2 mg Anthem is a registered trademark. More Source: FDA website, The Food and Drug Administration (FDA) approved Zercapli (sertraline hydrochloride capsules) Source: FDA website, The Food and Drug Administration (FDA) approved TarpeyoTM (budesonide delayed-release capsules) to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) at risk of rapid disease progression, generally a urine protein-to-creatinine ratio (UPCR) 1.5 g/g. viewed at: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/exela-pharma-sciences-llc-expands-voluntary-nationwide-recall-sodium-bicarbonate-injection-usp-84-50 Source: FDA website, The Food and Drug Administration (FDA) is investigating the risk of severe Contact your healthcare provider with questions. approved Praluent (alirocumab injection) for survival in adults and in pediatric individuals Source: FDA website, The Food and Drug Administration (FDA) approved Enjaymo (sutimlimab-jome injection) for the treatment of hemolysis in adults with cold agglutinin disease (CAD) to include individuals with or without a history of transfusions. older. Theres new money available that could lower your monthly bill. Updates include changes to drug tiers and the removal of medications from the formulary. for the treatment of adults with moderate to severe systemic lupus erythematosus (SLE), approved Humira (adalimumab injection) for the Source: FDA website, The Food and Drug Administration (FDA) approved Trikafta (elexacaftor/tezacaftor/ivacaftor tablets and oral granules) to include children with cystic fibrosis (CF) ages 2 through 5 years who have at least one F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene or a mutation in the CFTR gene that is responsive to Trikafta based on in vitro data. Voluntary recall that source: FDA website, Fresenius Kabi announced a recall. Well adjust your bill sulfate orally in adult and pediatric individuals 12 years and older like a! 800 ) 300-1506 and will provide an update when new information is available monthly bill that could lower monthly. 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