Dr. Chinta Sidharthan, medical and science writer of AZoNetwork | ResearchGate
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Patient Daily | Jun 4, 2025

Doctor on compounded medications: They 'meet individual patient needs when commercial drugs are unsuitable'

Dr. Chinta Sidharthan, a medical and science writer at AZoNetwork, said that compounded medications are crucial for patient-specific needs and evolve with updated oversight and practices. This statement was made in a scientific article.

"Compounded medications are formulations created to meet individual patient needs when commercial drugs are unsuitable, unavailable, or intolerable," said Sidharthan, Doctor, according to Medical News. "Compounding allows for formulations to be free from these excipients. Poor compounding practices can result in contamination or incorrect dosages. The landscape of pharmaceutical compounding is evolving in response to regulatory, technological, and clinical trends."

Compounded medications are essential for patients who cannot use mass-produced drugs due to allergies, specific dosage requirements, or drug unavailability. According to News-Medical.net, compounding provides therapeutic solutions by customizing medications to individual patient needs, such as altering dosage forms or excluding allergens. This personalization ensures that patients receive effective treatments tailored to their unique health conditions.

Compounded drugs play a significant role in managing chronic conditions, pediatric and geriatric care, and rare diseases. A study published in the Journal of Pharmaceutical Policy and Practice highlights that pharmacists often compound medicinal products to meet the special needs of patients with rare diseases, especially when no authorized treatments are available. This practice ensures that vulnerable populations receive necessary and effective therapies.

Regulatory frameworks distinguish between 503A and 503B compounding pharmacies. According to The FDA Group, 503A pharmacies compound medications based on individual prescriptions and are regulated by state boards of pharmacy, while 503B outsourcing facilities can produce larger batches without patient-specific prescriptions and must comply with current Good Manufacturing Practices (CGMP) under FDA oversight. This distinction ensures appropriate regulatory measures are applied based on the scale and scope of compounding activities.

Sidharthan is a science writer and educator based in Bangalore, India, with a Ph.D. in evolutionary biology from the Indian Institute of Science. Her expertise encompasses evolutionary biology, genetics, and herpetology, and she has extensive experience in scientific research, teaching, and science communication. Dr. Sidharthan has authored numerous articles and is passionate about science education, wildlife, and conservation.

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