Receiving a diagnosis of pulmonary tuberculosis (TB) can be frightening and stressful. It is a serious infection that primarily affects the lungs, often leading to persistent coughing, extreme fatigue, fever, and unintended weight loss. These physical symptoms can make simple daily tasks feel exhausting, while the contagious nature of the disease often leads to feelings of isolation. However, it is important to know that TB is curable. With the right medical care and adherence to treatment, patients can fully recover and return to their normal lives.

Treatment is critical not only to cure the individual but also to protect the community. The primary goal is to kill the Mycobacterium tuberculosis bacteria, stop the progression of the disease, and prevent the development of drug-resistant strains. Because TB bacteria grow slowly and can hide in the body, treatment takes much longer than typical bacterial infections. Plans are strictly tailored to the patient, depending on whether the TB strain is sensitive to standard drugs or resistant to them (World Health Organization, 2022).

Overview of treatment options for Pulmonary Tuberculosis

The cornerstone of TB management is a prolonged course of antibiotic combination therapy. Treatment typically lasts a minimum of six to nine months to ensure all bacteria, including those in a dormant state, are eradicated. The process is generally divided into two phases: an intensive phase to rapidly reduce the number of bacteria, followed by a continuation phase to eliminate any remaining germs.

For most patients, medication is the sole treatment required. In rare cases where complications have severely damaged the lungs, surgery might be considered, but this is not standard for uncomplicated cases. The success of the treatment relies almost entirely on taking every dose exactly as prescribed. Missing doses allows the bacteria to mutate and become resistant to drugs, making the infection much harder to cure.

Medications used for Pulmonary Tuberculosis

For standard, drug-susceptible TB, the first-line treatment involves a combination of four specific antibiotics often referred to as “RIPE” therapy. This regimen includes isoniazid, rifampin, pyrazinamide, and ethambutol. These medications are typically taken all together for the first two months, followed by a combination of just isoniazid and rifampin for several more months.

If a patient has drug-resistant TB (MDR-TB), first-line drugs may not work. In these cases, doctors prescribe second-line medications. These can include fluoroquinolones (such as levofloxacin or moxifloxacin) and injectable agents like amikacin. Newer drugs, such as bedaquiline and linezolid, are also becoming standard for resistant cases.

Clinical experience suggests that patients often stop feeling sick and become non-infectious within a few weeks of starting treatment. However, the bacteria are still present in the body, which is why continuing the medication is non-negotiable (Centers for Disease Control and Prevention, 2016).

How these medications work

TB medications work by attacking the bacteria at different stages of their life cycle to prevent them from surviving or reproducing. Isoniazid and ethambutol target the bacterial cell wall, disrupting its structure and causing the bacteria to become unstable and die.

Rifampin works by interfering with the bacteria’s ability to create RNA, which is essential for producing the proteins the germ needs to survive. Pyrazinamide is unique because it targets the dormant bacteria that are “sleeping” inside the body’s cells, which are often resistant to other drugs. By combining these mechanisms, the treatment hits the infection from multiple angles, reducing the chance that any bacteria will survive and develop resistance.

Side effects and safety considerations

TB medications require monitoring due to potent side effects, mainly liver toxicity. Symptoms include nausea, vomiting, abdominal pain, or jaundice, and alcohol must be avoided.

Rifampin often causes a harmless orange-red discoloration of body fluids (urine, sweat, tears, saliva), which can stain. Ethambutol may rarely cause vision changes, prompting baseline eye exams. Isoniazid can cause peripheral neuropathy (tingling), often treated with Vitamin B6. Patients should seek immediate care for vision changes, severe stomach pain, or yellowing skin.

Since everyone’s experience with the condition and its treatments can vary, working closely with a qualified healthcare provider helps ensure safe and effective care.

References

  1. Centers for Disease Control and Prevention. https://www.cdc.gov
  2. Mayo Clinic. https://www.mayoclinic.org
  3. World Health Organization. https://www.who.int
  4. American Lung Association. https://www.lung.org

Medications for Pulmonary Tuberculosis

These are drugs that have been approved by the US Food and Drug Administration (FDA), meaning they have been determined to be safe and effective for use in Pulmonary Tuberculosis.

Found 8 Approved Drugs for Pulmonary Tuberculosis

Sirturo

Generic Name
Bedaquiline

Sirturo

Generic Name
Bedaquiline
SIRTURO is a diarylquinoline antimycobacterial drug indicated as part of combination therapy in the treatment of adult and pediatric patients (5 years and older and weighing at least 15 kg) with pulmonary tuberculosis (TB) due to Mycobacterium tuberculosis resistant to at least rifampin and isoniazid. SIRTURO is a diarylquinoline antimycobacterial drug indicated as part of combination therapy in adult and pediatric patients (5 years and older and weighing at least 15 kg) with pulmonary tuberculosis (TB) due to Mycobacterium tuberculosis resistant to at least rifampin and isoniazid. ( 1 ) Limitations of Use : Do not use SIRTURO for the treatment of latent, extra-pulmonary or drug-sensitive TB or for the treatment of infections caused by non-tuberculous mycobacteria. ( 1 ) Limitations of Use Do not use SIRTURO for the treatment of: Latent infection due to Mycobacterium tuberculosis ( M. tuberculosis ) Drug-sensitive pulmonary TB Extra-pulmonary TB Infections caused by non-tuberculous mycobacteria.

Priftin

Generic Name
Rifapentine

Priftin

Generic Name
Rifapentine
PRIFTIN is a rifamycin antimycobacterial drug indicated in patients 12 years of age and older for the treatment of active pulmonary tuberculosis (TB) caused by Mycobacterium tuberculosis in combination with one or more antituberculosis (anti-TB) drugs to which the isolate is susceptible.

MethylPREDNISolone

Brand Names
Solu-Medrol MethylPREDNISolone, Solu-Medrol, Medrol

MethylPREDNISolone

Brand Names
Solu-Medrol MethylPREDNISolone, Solu-Medrol, Medrol
When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of Methylprednisolone Sodium Succinate for Injection, USP, is indicated as follows: Allergic states Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.

Pretomanid

Generic Name
Pretomanid

Pretomanid

Generic Name
Pretomanid
Limited Population: Pretomanid Tablet is indicated, as part of a combination regimen with bedaquiline and linezolid for the treatment of adults with pulmonary tuberculosis (TB) resistant to isoniazid, rifamycins, a fluoroquinolone and a second line injectable antibacterial drug OR adults with pulmonary TB resistant to isoniazid and rifampin, who are treatment-intolerant or nonresponsive to standard therapy. Approval of this indication is based on limited clinical safety and efficacy data. This drug is indicated for use in a limited and specific population of patients. Limitations of Use: Take Pretomanid Tablets are not indicated in patients with: o Drug-sensitive (DS) TB o Latent infection due to Mycobacterium tuberculosis. o Extra-pulmonary infection due to Mycobacterium tuberculosis. o TB resistant to isoniazid and rifampin who are responsive to standard therapy and not treatment-intolerant o TB with known resistance to any component of the combination, Safety and effectiveness of Pretomanid Tablets have not been established for its use in combination with drugs other than bedaquiline and linezolid as part of the recommended dosing regimen [see Dosage and Administration.

Kenalog

Brand Names
Lidolog, Mlk F3, Mlk F1, Pro-C-Dure 6, Bupivilog

Kenalog

Brand Names
Lidolog, Mlk F3, Mlk F1, Pro-C-Dure 6, Bupivilog
Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including triamcinolone acetonide injectable suspension is indicated for intramuscular use as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders: Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases: To tide the patient over a critical period of the disease in regional enteritis and ulcerative colitis. Hematologic disorders: Acquired (autoimmune) hemolytic anemia, Diamond-Blackfan anemia, pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous: Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used with appropriate antituberculous chemotherapy. Neoplastic diseases: For the palliative management of leukemias and lymphomas. Nervous system: Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor or craniotomy. Ophthalmic diseases: Sympathetic ophthalmia, temporal arteritis, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases: To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases: Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders: As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, polymyositis and systemic lupus erythematosus. Intra-Articular The intra-articular or soft tissue administration of triamcinolone acetonide injectable suspension is indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis, acute and subacute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, synovitis of osteoarthritis.
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