The Drug Information Centre (DIC) of Dr D Y Patil College Of Pharmacy Akurdi is a student-driven initiative dedicated to promoting safe and rational use of medicines. The centre is managed by Pharm.D students under the supervision of faculty members, ensuring that all information provided is authentic, unbiased, and evidence-based.
By referring to standard and trusted sources such as WHO guidelines, Micromedex, Lexicomp, FDA updates, and peer-reviewed journals, the centre provides reliable drug-related information to:
Our Objectives:
The student-led nature of this centre not only benefits patients and healthcare providers but also enhances the practical learning experience of our students, preparing them as future pharmacists and clinical experts.
Drug Monographs
The Drug Monographs section provides concise, evidence-based, and easy-to-understand information about commonly used medicines. Each monograph is carefully prepared by our Pharm.D and pharmacy students, under faculty supervision, by referring to standard references such as WHO, Micromedex, Lexicomp, and peer-reviewed journals.
These monographs cover essential details including:
This section is designed to support students, healthcare professionals, and the community by promoting safe and rational drug use.
Example:
Sample Drug Monograph
Generic Name
Paracetamol (INN), also known as Acetaminophen (USAN)
Brand Names
Crocin®, Calpol®, Dolo-650®, Tylenol®
Pharmacological Class
Analgesic and Antipyretic
Mechanism of Action
Paracetamol inhibits prostaglandin synthesis in the central nervous system and works on the hypothalamic heat-regulating center, leading to pain relief and fever reduction.
Indications
Fever (pyrexia)
Mild to moderate pain (e.g., headache, myalgia, osteoarthritis, toothache)
Adjunct in severe pain (with opioids or NSAIDs)
Dosage & Administration
Adults: 500 mg – 1 g every 4–6 hours (maximum 4 g/day)
Children (6–12 years): 250–500 mg every 4–6 hours (maximum 60 mg/kg/day)
Route: Oral, IV, or rectal
Contraindications
Hypersensitivity to paracetamol
Severe liver impairment or active liver disease
Precautions
Use with caution in patients with chronic alcohol use, liver disease, or malnutrition.
Avoid exceeding recommended dose due to hepatotoxicity risk.
Adverse Drug Reactions (ADRs)
Common: Nausea, rash
Rare: Allergic reactions, blood dyscrasias
Serious: Hepatotoxicity (with overdose)
Drug Interactions
Alcohol → ↑ risk of liver damage
Warfarin → ↑ anticoagulant effect with chronic use
Enzyme-inducing drugs (e.g., carbamazepine, phenytoin) → ↑ hepatotoxicity risk
Patient Counseling Points
Do not exceed the recommended dose.
Avoid alcohol while taking paracetamol.
Report symptoms of liver damage (yellowing of skin/eyes, dark urine).
Safe in pregnancy and breastfeeding when used at recommended doses.
References
RX Express Intro:
RX Express is the dedicated news and updates corner of our Drug Information Centre. This section brings you the latest trends, research highlights, and updates in the fields of Pharm.D, pharmacy practice, medicine, and pharmaceutical sciences.
Here, students and faculty curate reliable, authentic, and up-to-date information from standard sources such as medical journals, regulatory bodies (FDA, EMA, CDSCO), WHO, and leading healthcare organizations.
What You’ll Find in RX Express:
Through RX Express, we aim to keep our readers informed, connected, and inspired by the rapidly evolving world of pharmacy and healthcare.
Example:
FDA Approves First Oral GLP-1 Agonist for Type 2 Diabetes
Published: August 2025
The U.S. Food and Drug Administration (FDA) has recently approved oral semaglutide (brand name: Rybelsus®) as the first oral GLP-1 receptor agonist for the treatment of type 2 diabetes. This breakthrough provides patients an alternative to injectable GLP-1 agonists, offering improved convenience and adherence.
Clinical trials have demonstrated that oral semaglutide significantly reduces HbA1c levels and supports weight management, making it a valuable addition to current diabetes therapy options. Healthcare professionals are advised to consider its use in patients who require better glycemic control and prefer oral therapy over injections.
📌 Reference:
U.S. Food and Drug Administration (FDA). (2019). FDA approves first oral GLP-1 treatment for type 2 diabetes. Retrieved from https://www.fda.gov/news-events/press-announcements/fda-approves-first-oral-glp-1-treatment-type-2-diabetes