# Nationwide assessment of community pharmacists’ practices and atorvastatin–drug interactions in Egypt

**Authors:** Mohammed G. Maslub, Mahasen Ali Radwan, Nur Aizati Athirah Daud, Zeyad Ali Abd-Alla, Marwa Adham El-Mohamdy

PMC · DOI: 10.1038/s41598-026-40872-1 · 2026-03-27

## TL;DR

This study assesses how well Egyptian community pharmacists manage atorvastatin drug interactions and identifies areas for improvement in safety practices.

## Contribution

The study provides a nationwide evaluation of pharmacists' practices and reported drug interactions with atorvastatin in Egypt.

## Key findings

- Pharmacists frequently counsel patients and use web-based resources but less often use structured DDI screening tools.
- Female pharmacists and those with diplomas showed better adherence to safety practices than their counterparts.
- Common DDIs included cyclosporine, clarithromycin, and azithromycin, with regional variations in frequency.

## Abstract

Atorvastatin (ATV) is widely prescribed in Egypt, where cardiovascular disease remains the leading cause of mortality; however, it is prone to clinically significant drug–drug interactions (DDIs). This national cross-sectional study evaluated community pharmacists’ (CPs’) knowledge, practice behaviors, and reported rates of ATV-related DDIs across Egypt. A total of 973 licensed pharmacists completed a validated survey. The mean cumulative practice score was 7.2 ± 1.91, indicating high adherence to recommended safety practices. Frequently reported roles included targeting polypharmacy patients (80.1%), initiating single-drug therapy when appropriate (82.2%), counseling patients about adverse effects (85.1%), and using web-based drug-information resources (88.2%), whereas structured DDI screening tool use was less common (46.1%). Compared with male pharmacists, female pharmacists presented significantly higher cumulative practice scores (7.52 ± 1.59 vs. 7.08 ± 1.99; p = 0.016), and diploma holders scored higher than Ph.D. holders did (7.47 ± 1.81 vs. 6.82 ± 1.87; adjusted p = 0.02). High-frequency encounters were reported for major DDIs with cyclosporine (49.3%) and clarithromycin (45.8%) and for moderate DDIs with digoxin (42.2%), phenytoin (41.0%), and azithromycin (40.5%). Regional variation showed higher interaction frequencies in Upper Egypt and the Delta. Strengthening pharmacist stewardship programs and expanding standardized DDI screening approaches may improve ATV safety.

## Linked entities

- **Chemicals:** atorvastatin (PubChem CID 60823), cyclosporine (PubChem CID 5284373), clarithromycin (PubChem CID 84029), digoxin (PubChem CID 2724385), phenytoin (PubChem CID 1775), azithromycin (PubChem CID 447043)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}
- **Diseases:** rhabdomyolysis (MESH:D012206), metabolic complications (MESH:D020739), DDIs (MESH:D000081015), CVD (MESH:D002318), toxicity (MESH:D064420), chronic liver disease (MESH:D008107), heart failure (MESH:D006333), lipid abnormalities (MESH:D011017), DIs (MESH:D003643), disease (MESH:D004194), epilepsy (MESH:D004827), CP (MESH:D002972), myotoxicity (MESH:D000081030), Dyslipidemia (MESH:D050171), myopathy (MESH:D009135)
- **Chemicals:** clopidogrel (MESH:D000077144), phenytoin (MESH:D010672), fenofibrate (MESH:D011345), lipid (MESH:D008055), cyclosporine (MESH:D016572), pectin (MESH:D010368), ketoconazole (MESH:D007654), fluconazole (MESH:D015725), niacin (MESH:D009525), azithromycin (MESH:D017963), ATV (MESH:D000069059), leflunomide (MESH:D000077339), gemfibrozil (MESH:D015248), erythromycin (MESH:D004917), macrolide (MESH:D018942), nefazodone (MESH:C051752), digoxin (MESH:D004077), CP (-), cholesterol (MESH:D002784), fluvoxamine (MESH:D016666), clarithromycin (MESH:D017291), amiodarone (MESH:D000638)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** ECH- — Homo sapiens (Human), Chronic myelogenous leukemia, BCR-ABL1 positive, Cancer cell line (CVCL_XN33)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031436/full.md

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Source: https://tomesphere.com/paper/PMC13031436