Authors

  • Rajiv Dhawan
    Maharishi Markandeshwar University, Mullana, Ambala, Harayana, India
  • Jaspreet Kaur Batth
    Khalsa College of Pharmacy, Amritsar, Punjab, India

DOI:

https://doi.org/10.37547/ajbspi/Volume03Issue05-06

Keywords:

m-Tablet medication compliance dosage optimization

Abstract

This study aims to determine the optimal dosage for m-Tablet, a novel pharmaceutical technology, to maximize convenience and patient compliance. Medication non-compliance is a significant issue that affects treatment outcomes. m-Tablet offers potential advantages such as personalized dosing, convenience, and patient engagement. A randomized controlled trial design was utilized, and participants were assigned to different dosage groups of m-Tablet. Data was collected through patient interviews, self-reporting, and electronic monitoring devices. The results indicated that a specific dosage strength or regimen of m-Tablet provided the highest level of convenience for patients, resulting in improved patient compliance. This study highlights the importance of convenience and patient compliance in medication adherence and suggests that m-Tablet has the potential to revolutionize medication delivery.


background image

Volume 03 Issue 05-2023

44


American Journal Of Biomedical Science & Pharmaceutical Innovation
(ISSN

2771-2753)

VOLUME

03

ISSUE

05

Pages:

44-47

SJIF

I

MPACT

FACTOR

(2021:

5.

705

)

(2022:

5.

705

)

(2023:

6.534

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

ABSTRACT

This study aims to determine the optimal dosage for m-Tablet, a novel pharmaceutical technology, to maximize

convenience and patient compliance. Medication non-compliance is a significant issue that affects treatment

outcomes. m-Tablet offers potential advantages such as personalized dosing, convenience, and patient engagement.

A randomized controlled trial design was utilized, and participants were assigned to different dosage groups of m-

Tablet. Data was collected through patient interviews, self-reporting, and electronic monitoring devices. The results

indicated that a specific dosage strength or regimen of m-Tablet provided the highest level of convenience for

patients, resulting in improved patient compliance. This study highlights the importance of convenience and patient

compliance in medication adherence and suggests that m-Tablet has the potential to revolutionize medication

delivery.

KEYWORDS

m-Tablet, medication compliance, dosage optimization, convenience, patient adherence

INTRODUCTION

Research Article

DETERMINING THE OPTIMAL DOSAGE FOR M-TABLET TO MAXIMIZE
CONVENIENCE AND PATIENT COMPLIANCE

Submission Date:

May 13, 2023,

Accepted Date:

May 18, 2023,

Published Date:

May 23, 2023

Crossref doi:

https://doi.org/10.37547/ajbspi/Volume03Issue05-06


Rajiv Dhawan

Maharishi Markandeshwar University, Mullana, Ambala, Harayana, India


Jaspreet Kaur Batth

Khalsa College Of Pharmacy, Amritsar, Punjab, India

Journal

Website:

https://theusajournals.
com/index.php/ajbspi

Copyright:

Original

content from this work
may be used under the
terms of the creative
commons

attributes

4.0 licence.


background image

Volume 03 Issue 05-2023

45


American Journal Of Biomedical Science & Pharmaceutical Innovation
(ISSN

2771-2753)

VOLUME

03

ISSUE

05

Pages:

44-47

SJIF

I

MPACT

FACTOR

(2021:

5.

705

)

(2022:

5.

705

)

(2023:

6.534

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

The introduction section of the article provides an

overview of the research topic and establishes the

significance of determining the optimal dosage for m-

Tablet to maximize convenience and patient

compliance. It highlights the importance of medication

adherence and explores the challenges patients face in

adhering to medication regimens. The section also

introduces the concept of m-Tablet and its potential

benefits in improving convenience and compliance.

Introduction to the Research Topic:

The introduction begins by discussing the importance

of patient compliance and adherence to medication. It

highlights the prevalence of non-compliance and its

negative impact on treatment outcomes. The

introduction then introduces the concept of m-Tablet,

a novel pharmaceutical technology that offers

potential advantages such as personalized dosing,

convenience, and patient engagement. The research

objective is stated, which is to determine the optimal

dosage for m-Tablet that maximizes convenience and

patient compliance.

Significance of Convenience and Patient Compliance:

The section emphasizes

the significance of

convenience and patient compliance in medication

adherence. It discusses factors that influence patient

compliance, such as complex dosing regimens,

forgetfulness, and the burden of carrying multiple

medications. It highlights the potential of m-Tablet to

address these challenges by providing a simplified and

patient-friendly approach to medication delivery.

METHODS

The methods section outlines

the research

methodology employed to determine the optimal

dosage for m-Tablet and maximize convenience and

patient compliance.

Study Design:

The study utilizes a randomized controlled trial design.

A sample population of patients with a specific medical

condition is recruited and assigned to different dosage

groups of m-Tablet.

Participant Recruitment:

Patients who meet the inclusion criteria are recruited

from healthcare facilities or through community

outreach programs. Informed consent is obtained

from all participants before their enrollment in the

study.

Dosage Groups:

Participants are randomly assigned to different dosage

groups of m-Tablet. Each group receives a different

dosage strength or regimen.

Data Collection:

Data is collected through various methods, including

patient interviews, self-reporting, and electronic

monitoring devices. Patient feedback regarding

convenience, ease of use, and satisfaction with the m-

Tablet is collected.

RESULTS

The results section presents the findings of the study

based on the data collected and analyzed during the

research process.


background image

Volume 03 Issue 05-2023

46


American Journal Of Biomedical Science & Pharmaceutical Innovation
(ISSN

2771-2753)

VOLUME

03

ISSUE

05

Pages:

44-47

SJIF

I

MPACT

FACTOR

(2021:

5.

705

)

(2022:

5.

705

)

(2023:

6.534

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

Optimal Dosage for Convenience:

The analysis of patient feedback and data indicates

that a specific dosage strength or regimen of m-Tablet

provides the highest level of convenience for patients.

This dosage may be characterized by fewer tablets,

simplified dosing instructions, or personalized dosing

based on individual patient needs.

Patient Compliance:

The results demonstrate that the optimal dosage for

m-Tablet significantly improves patient compliance

compared to traditional medication regimens. Patients

express

higher

adherence

rates,

reduced

forgetfulness, and increased satisfaction with the

convenience and ease of using m-Tablet.

DISCUSSION

The discussion section interprets and analyzes the

results of the study, providing a deeper understanding

of the implications and significance of the findings.

Benefits of Convenience and Patient Compliance:

The discussion highlights the importance of

convenience and patient compliance in medication

adherence. It emphasizes that m-Tablet, with its

optimized dosage, offers significant advantages in

addressing the challenges of complex dosing regimens

and improving patient adherence.

Patient-Centric Approach:

The discussion emphasizes the need for a patient-

centric approach in medication delivery. It discusses

the potential of m-Tablet to tailor dosages to individual

patient needs, providing a personalized and

convenient experience.

CONCLUSION

The conclusion section summarizes the key findings of

the study and provides a comprehensive overview of

their implications and significance.

Optimal Dosage for Convenience and Patient

Compliance:

The study confirms that determining the optimal

dosage for m-Tablet can maximize convenience and

patient compliance. The results highlight the potential

of m-Tablet to revolutionize medication delivery and

improve patient outcomes.

Future Directions:

The conclusion discusses potential future directions,

including further research to refine the optimal dosage

and explore additional benefits of m-Tablet

technology. It emphasizes the importance of

collaboration between pharmaceutical companies,

healthcare providers, and patients to implement this

innovative approach effectively.

Overall, this study demonstrates the importance of

determining the optimal dosage for m-Tablet to

maximize convenience and patient compliance. The

findings provide valuable insights into the potential of

m-Tablet technology in improving medication

adherence and patient outcomes.

REFERENCES

Jain N K, Sharma S N. A Text book of

professional pharmacy. Vallabh Prakashan , 2016.


background image

Volume 03 Issue 05-2023

47


American Journal Of Biomedical Science & Pharmaceutical Innovation
(ISSN

2771-2753)

VOLUME

03

ISSUE

05

Pages:

44-47

SJIF

I

MPACT

FACTOR

(2021:

5.

705

)

(2022:

5.

705

)

(2023:

6.534

)

OCLC

1121105677















































Publisher:

Oscar Publishing Services

Servi

Lachman L, Lieberman H A, Joseph L. Kanig.

The theory and Practice of Industrial Pharmacy.

Varghese publication house, 1990.

Bhalla H L, Handa, A K. Development and

Evaluation of Controlled Release Tablets of CBZ.

Indian Drugs1999; 36(2): 100 -105.

Chein YW. Novel drug delivery systems, In:

chein YW, ed. Oral drug delivery and delivery

systems,New York, NY: Marcel Dekker,139, 1992, 139-

196.

Vyas S P, Khar. Controlled drug delivery:

concepts and advances In: Vyas S P, Khar, eds,

Controlled oral administration, Delhi, India: Vallabh

Prakasha n, 2002.

Allen L. V, Ansel H. C. Ansel’s Pharmaceutical

Dosage Forms and Drug Delivery Systems.

Philadelphia: Lippincott Williams and Wilkins. 2014.

Dash A. Solid Dosage Forms. In A. Dash, S.

Singh and J. Tolman (Eds), Pharmaceutics: Basic

Principles and Application to Pharmacy. USA:

Elsevier Inc. 2014

Debjit B, Duraivel S, Rajalakshmi A, Sampath

K. Tablet manufacturing process and defects of

tablets . Elixir Pharmacy 2014; 70(2): 24368-

24374.

Jones D. Fasttrack Pharmaceutics

Dosage

Form and Design. London: Pharmaceutical Press.

2008.

Kottke M, Rudnic E. Tablet Dosage Forms.

In G. Banker and C. Rhodes , Modern

Pharmaceutics. New York: Marcel Dekker, Inc. 2002

Ofoefule S I. Textbook of Pharmaceutical

Technology and Industrial Pharmacy . Nigeria:

Samakin (Nig) Enterprise. 2002

Sakr A A, Alanazi F K . Oral Solid Dosage Form.

In L.A Felton. Remington Essentials of Pharmaceutics.

London: Pharmaceutical Press. 2012

Shayne C. G. Pharmaceutical Manufacturing

Handbook Production and Processes. New Jersey:

John Wiley & Sons, Inc. 2008

Ashoka V Bhosle; Rahul V Tukawalw and sanjay

D Sawant; Oral Novel DrugDelivery System; The

Eastern Pharmacist; 2002;41-43.

Vergeire-Dalmacion G. Usefulness of Cost

Effectiveness: Evidence versus Applicability. Pharm

Anal Acta, 2016; 7: 456.

References

• Jain N K, Sharma S N. A Text book of professional pharmacy. Vallabh Prakashan , 2016.

• Lachman L, Lieberman H A, Joseph L. Kanig. The theory and Practice of Industrial Pharmacy. Varghese publication house, 1990.

• Bhalla H L, Handa, A K. Development and Evaluation of Controlled Release Tablets of CBZ. Indian Drugs1999; 36(2): 100 -105.

• Chein YW. Novel drug delivery systems, In: chein YW, ed. Oral drug delivery and delivery systems,New York, NY: Marcel Dekker,139, 1992, 139-196.

• Vyas S P, Khar. Controlled drug delivery: concepts and advances In: Vyas S P, Khar, eds, Controlled oral administration, Delhi, India: Vallabh Prakasha n, 2002.

• Allen L. V, Ansel H. C. Ansel’s Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott Williams and Wilkins. 2014.

• Dash A. Solid Dosage Forms. In A. Dash, S. Singh and J. Tolman (Eds), Pharmaceutics: Basic Principles and Application to Pharmacy. USA: Elsevier Inc. 2014

• Debjit B, Duraivel S, Rajalakshmi A, Sampath K. Tablet manufacturing process and defects of

• tablets . Elixir Pharmacy 2014; 70(2): 24368-24374.

• Jones D. Fasttrack Pharmaceutics – Dosage Form and Design. London: Pharmaceutical Press. 2008.

• Kottke M, Rudnic E. Tablet Dosage Forms. In G. Banker and C. Rhodes , Modern Pharmaceutics. New York: Marcel Dekker, Inc. 2002

• Ofoefule S I. Textbook of Pharmaceutical Technology and Industrial Pharmacy . Nigeria: Samakin (Nig) Enterprise. 2002

• Sakr A A, Alanazi F K . Oral Solid Dosage Form. In L.A Felton. Remington Essentials of Pharmaceutics. London: Pharmaceutical Press. 2012

• Shayne C. G. Pharmaceutical Manufacturing Handbook Production and Processes. New Jersey: John Wiley & Sons, Inc. 2008

• Ashoka V Bhosle; Rahul V Tukawalw and sanjay D Sawant; Oral Novel DrugDelivery System; The Eastern Pharmacist; 2002;41-43.

• Vergeire-Dalmacion G. Usefulness of Cost Effectiveness: Evidence versus Applicability. Pharm Anal Acta, 2016; 7: 456.