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Author(s): Tanvi Madane*1, Dr. Rohini Chavan2

Email(s): 1tanvimadane2002@gmail.com

Address:

    Department of Pharmacy Practice, PES’s Modern College of Pharmacy, Nigdi, Pune-411044, India.

Published In:   Volume - 5,      Issue - 3,     Year - 2026


Cite this article:
Tanvi Madane, Dr. Rohini Chavan. A Narrative Review of the Prevalence, Types, and Contributing Factors of Drug-Related Problems in Hospitals. IJRPAS, March 2026; 5(3): 25-43.

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A Narrative Review of the Prevalence, Types, and Contributing Factors of Drug-Related Problems in Hospitals.

Tanvi Madane*, Dr. Rohini Chavan

Department of Pharmacy Practice, PES’s Modern College of Pharmacy, Nigdi, Pune-411044, India.

 

*Correspondence: tanvimadane2002@gmail.com

DOI: https://doi.org/10.71431/IJRPAS.2026.5303     

Article Information

 

Abstract

Review Article Received: 05/03/2026

Accepted:25/03/2026

Published:31/03/2026

 

Keywords

Adverse drug reactions(ADR); drug-related problems(DRP); drug-drug interaction; medication errors;  polypharmacy

 

Medication is one of the most commonly used treatments used in modern healthcare; its use is frequently linked to drug-related problems, such as medication errors, adverse drug reactions, and inappropriate prescribing.  Because concurrent conditions, clinical complications, and poly pharmacy are common in hospital settings, these issues can have a substantial impact on treatment outcomes and the safety of patients.  To categorize the most widely used DRPs in clinical settings, determine which drug classes are most commonly associated, and emphasize risk factors and successful interventions, a systematic review was carried out.  PubMed, Scopus, Google Scholar, Web of Science, and the Cochrane Library were used to conduct a thorough literature search for research published between 2018 and 2025.Data on study characteristics, DRP types and prevalence, risk factor, and interventions were extracted from relevant articles on medication errors, adverse drug events, and drug-related hospital admissions.  The most common DRPs, according to the review findings, were Drug choice problem (Inappropriate drug selection, untreated indications), Dosing problem (incorrect dose selection), adverse drug events, and drug-drug interactions. The main groups of drugs involved were antimicrobial, cardiovascular agents, antidiabetic drugs, and drugs that affect the central nervous system. Polypharmacy, advanced age, several comorbidities, extended hospitalization, and clinical complexity were all contributing factors.  Finally, DRPs continue to be a prevalent and avoidable issue in patient care.  Improving prescribing procedures, encouraging interdisciplinary cooperation, and fortifying clinical pharmacy services are all crucial to lowering DRPs, boosting patient safety, and enhancing therapeutic results.

 

INTRODUCTION   

In pharmacology, a drug is described as any chemical substance, excluding food, that produces measurable physiological effects in living organisms [1]. Pharmacotherapy remains the most widely used medical intervention and significantly improves patient outcomes. Nevertheless, along with its therapeutic benefits, medication use also carries the possibility of harm, making patient safety a priority [2,3]. Adverse drug use can result in drug related problems (DRPs), which are described as "events or circumstances involving medication that actually or possibly cause problems with desired health outcomes." [4-6]. Medication Errors (MEs), which are defined as "any avoidable occurrence that may cause or result in incorrect application of medication or patient harm," are closely related to this. [7]. Though they can occur at any

Drug related problem

Definition

Drug dose too high

Drug dose too high occurs when the dosage of a drug is greater than required, resulting in actual or potential harm to the patient. This can be due to prescribing errors, lack of appropriate dose adjustment (e.g., in renal/hepatic impairment), or drug interactions increasing drug levels." [25]

Drug dose too low

Drug dose too low occurs when a patient receives a dose of medication that is less than what is required to produce the desired therapeutic effect. This may be due to inappropriate dosage, frequency, duration, drug interactions reducing effect, or patient-specific factors such as weight or organ function."[25].

Administration error (including timing relative to meals)

Errors in the method or timing of drug administration, including incorrect route, technique, or timing (e.g., before/after meals) that may alter absorption or efficacy.

Drug interactions

"A change in a drug's effect on the human body when the medication is taken with a second drug" is the definition of a drug-drug interaction [26].

Adverse drug reaction

According to the WHO, an adverse drug reaction (ADR) is any unpleasant and unexpected reaction to a medication that happens at dosages used for human prophylaxis, diagnosis, or treatment, excluding failure to accomplish the intended purpose [27].

Inappropriate indications for diagnosis

“Inappropriate indication occurs when a drug is prescribed for a condition for which it is not clinically indicated or lacks evidence-based justification. This includes prescribing drugs for conditions they are not approved or recommended for.”

Inappropriate indications for patients

“Inappropriate indication for a patient occurs when a drug is prescribed despite the absence of a proper, evidence-based medical need in that individual, which may result in unnecessary exposure to adverse effects and increased treatment costs.”

Incorrect Dosage form

"Using a drug in a way that is inappropriate for the patient's condition, capacity to use, or planned route results in suboptimal therapy or a risk of harm." This is known as "incorrect dosage form."

\stage of the use of  medications, including prescriptions, transcription, dispensing, and administration, prescription and administration errors are the most frequently reported [8]. Common examples of DRPs

Table 1) include inappropriate dosage (either excessive or subtherapeutic), irrational drug selection, Drug-drug interactions (DDIs), Adverse drug reactions (ADRs), and non-adherence linked to psychological,

behavioural, or social causes [9-11].

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

To better understand and categorise DRPs, several classification frameworks have been introduced. The influential model proposed by Hepler and Strand identifies categories such as untreated indications, adverse drug reactions, improper drug selection, subtherapeutic and excessive dosages, drug interactions, failure to receive medication, and drug use without a valid indication [12]. More structured systems, such as the Pharmaceutical Care Network Europe (PCNE) classification and Cipolle’s framework, extend this approach by examining causes, interventions, and outcomes [13]. DRPs and medication errors pose a serious public health concern on a global basis, as they increase morbidity, lengthen hospital stays, and drive up medical expenses. Research indicates that 5–10% of hospital stays are directly related to preventable medication-related incidents, and 10 to 20 per cent of hospitalised patients have at least one ADR [14]. The likelihood of errors is even higher in high-acuity settings such as intensive care units, operating theatres, and emergency departments, where treatment complexity and time-sensitive decisions are routine [15,16]. For example, a study conducted in England in 2021 reported ADRs in 12.6% of psychiatric inpatients, illustrating the widespread impact of DRPs across specialities [17].

In India, the scenario is similarly concerning. According to Professor Jha's estimations, the British Medical Journal highlighted the fact that there are roughly 5.2 million medical errors per year. Contributing factors include a shortage of trained healthcare professionals and nursing staff, inadequate resource allocation, and limited systems for monitoring clinical outcomes [18]. Several patient-related and treatment-related risk factors further increase the likelihood of DRPs. These include polypharmacy, comorbidities, age-associated pharmacokinetic and pharmacodynamic alterations, and the complexity of hospital-based therapeutic regimens [19,20]. Older adults are especially vulnerable due to multiple chronic illnesses, polypharmacy, and heightened susceptibility to ADRs and DDIs [21]. The impact of DRPs extends beyond clinical harm, often impairing quality of life, diminishing adherence to prescribed regimens, and contributing to recurrent hospital readmissions [22]. Clinical pharmacists have an essential role in addressing this burden, as their active involvement in multidisciplinary teams has been shown to reduce prescribing errors, enhance medication safety, and optimise therapeutic results [23,24].

Considering the significant and largely preventable nature of DRPs, especially within hospital environments, a consolidated understanding is required to strengthen patient safety and ensure rational drug therapy. Although many studies have explored DRPs in specific departments or populations, there remains a need for a comprehensive and updated overview. The present review, therefore, aims to synthesise current evidence on DRPs in hospital settings, focusing on their definitions, classifications, prevalence, risk factors, clinical consequences, and strategies for effective detection and prevention.

MATERIALS AND METHODS

Using five online databases—PubMed, Scopus, Google Scholar, Web of Science, and the Cochrane Library—a systematic review of the literature was carried out on articles published in English between 2018 and 2025 (see Figure 1: PRISMA Flow Diagram). To identify and eliminate duplicate studies and those unrelated to the topic, a screening of titles and abstracts was conducted following the initial search.

The following search terms and Boolean operators were used: ("adverse drug events" OR "adverse drug reactions" OR "medication errors" OR "medication-related problems") AND ("hospital admissions" OR "hospitalisation") AND ("incidence" OR "prevalence").

Studies were included if they involved hospitalised patients (patient population) and reported DRPs such as adverse drug reactions, medication errors, or other medication-related issues. Eligible study designs included observational (cross-sectional, cohort, and case-control) and interventional studies. Studies were required to report clinical or epidemiological outcomes, such as the incidence, prevalence, or risk factors of medication-related problems. Case reports, editorials, commentaries, non-hospital-based studies, and non-English publications were excluded.

Data extracted from each included study comprised the author and year of publication, total number of patients, frequency of hospitalisation due to medication, type of medication-related issue (e.g., ADRs), identified risk factors, and reported interventions. To ensure consistency across studies, all DRPs were reclassified according to the Pharmaceutical Care Network Europe (PCNE) DRP classification system (version 9.1). Equivalent study terms were mapped to the nearest PCNE category.

The quality and risk of bias of the included studies were assessed using the Newcastle–Ottawa Scale (NOS) for observational studies and the ROBINS-I tool for interventional studies. Two reviewers independently performed the assessment, and discrepancies were resolved through consensus.

Identification of studies via databases and registers

Identification

Records identified from: Databases (n=100)

Records removed before screening:

Duplicate Records removed (n=20)

Records removed for other reasons (n=5)

Screening

Records screened (n=75)

Records exclude (n=25)

 

Records sought for retrieval (n=50)

Reports not retrieved(n=0)

Reports assessed for eligibility (n=50)

Reports excluded:

DRP was not mentioned (n=17)

Major contributing drugs was not mentioned (n= 13)

Studies included in review (n= 20)

Reports of included Studies

(n= 20)

Included

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


Fig. 1: Schematic form of identification and screening of the studies and literatures from the databases

 

RESULT

Twenty studies [Table 2] from eight countries published between 2018 and 2025 were included, with India accounting for the largest share (45%).  When taken as a whole, these studies examined over 25,000 prescriptions from different hospital settings, such as medical wards, intensive care units, and neonatal intensive care units.  DRPs were reported to be prevalent in 14% to 77% of cases (mean 46.8%).  Drug choice problem (Inappropriate drug selection (44.1%), untreated indications (20.9%)), Dosing problem (incorrect dose selection (32.8%)), ADE(28.6%), and DDIs(16.3%) were the most common DRP types.

The most frequently implicated drug class was antimicrobials (60–65%), followed by medications for the CNS (20–25%), cardiovascular (30–35%), and antidiabetic (25–30%).  Ceftriaxone, metronidazole, piperacillin-tazobactam, linezolid, colistin, insulin, metformin, and calcium channel blockers were among the frequently used medications.  An estimated 25–35% of DRPs were associated with improper use of antibiotics.  The most common risk factors were comorbidities like hypertension, diabetes, and renal impairment (55–65%) and polypharmacy (40–70%).

The Drug use process problems (prescription (45.1%), documentation (33.8%), and administration (21.1%)) phases were the most common times that medication errors were reported.  90% of studies reported clinical pharmacist involvement, with up to 99% of DRPs resolved through dose modification (27–33%), stopping inappropriate therapy (20–25%), or adding necessary treatment (15–20%).  The majority of unresolved DRPs (5–10%) were associated with complex clinical conditions.

Table 2: List of literatures.

Study N.

Reference

Country

Drug related problem

Problems on admission

Major contributing Drugs

Remark

1

[28]

India

Drug choice problem(14.54%),  andDrug drug interaction(6.36%) 

The   prevalent   comorbidities   were ischemic  heart  disease  (21.81%),  urinary  tract  infections (18.18%)andchronic   kidney   disease   (14.54%).

37.27% received monotherapy for T2DM, with Human Actrapid being the most common (70.73%).   Dual   therapy   (33.63%)   was   dominated   by Vildagliptin+Metformin   (29.72%)and triple   therapy (10%) most often involved Metformin+Voglibose+Glimepiride  (63.63%). Beta blockers (36.36%) and calcium channel blockers (37.27%) were common, with bisoprololaccounting for 23.63%.

DRPs have a major influence on how T2DM and HTN are managed, emphasizing the necessity of routine medication reviews and focused interventions to maximize therapeutic results in these patients.

2

[29]

India

Dosing problem, suboptimal drug treatment outcomes, and ambiguous issues

NR

Antihypertensives, proton pump inhibitors, furosemide, anticoagulants

DRPs are an emerging issue within the connes  of  the  health-care  system  and  should  be  scrutinized  to  avoid  negative outcomes.  A  stage-wise  analysis  of  patients  who  are  at  risk  will  ensure  better patient care

3

[30]

India

Drugchoice problem by the prescriber 193 (59.5%), drug-drug interactions (16.3%), Inappropriate drug formulations were prescribed for 7 (2.1%), Dosing problem were observed in 3 (0.9%),

NR

Ceftriaxone+Heparin, Azithromycin+ ondensetron,Formeterol+ ondensetron , Ibuprofen+ Ciprofloxacin, Haloperidol+ Promethazine

The current study emphasizes the importance of reporting DRPs to patients in order to provide better health care and advocates the significance of clinical pharmacists in pharmaceutical patient care.

4

[31]

Egypt

Drug treatment effects not optimal 714 (41.4%), Adversedrugevents455 (26.4%)

NR

Metronidazole, cefepime, linezolid, amikacin, meropenem, cefotaxime, piperacillin-tazobactam, ampicillin-sulbactam, caffeine, and dopamine

This study showed how important clinical pharmacists are in recognizing and addressing DRPs, which are prevalent in the NICU.

5

[32]

Turkey

Adverse drug events (ADEs) (77.18%),Drug choice problem(40.29%) and Dosing problem(54.36%),Drug introduction(35.43%)

Respiratory system problems (60.9%) and sepsis (72.2%), nephrotoxicity (48.57%), electrolyte disorders (17.14%), drug-induced thrombocytopenia (17.14%), liver enzyme increase (8.57%) and other causes (8.57%)

Heparin, linezolid, and piperacillin-tazobactam are a few medications that can cause thrombocytopenia.  The main medication that causes nephrotoxicity is colistin.  Hyperkalemia brought on by trimethoprim-sulfamethoxazole is an example of an electrolyte imbalance.

In this study, the importance of the clinical pharmacist in the determination and analysis of DRPs was emphasized. Clinical pharmacy services like the one described should be implemented widely to increase patient safety.

6

[33]

India

Adverse drug events(n = 933, 8.9%),  Drug interactions(20.1%) drug–disease interactions  (7.9%)

Pedal edema (6.6%), sedation (5.3%) and gastritis (5.2%)

Antihypertensives (24, 35.8%), neurological drugs (16, 23.8%) and antidiabetics (10, 14.9%).

One out of 10 prescriptions of older outpatients carries a DRP. New-onset metabolic and neurological disturbances should prompt a thorough drug history. A multifaceted holistic approach can prevent significant drug-related morbidity and requires future evaluation.

7

[34]

India

Drug Choice problem(Inappropriate choice 63 (14.82%),Similar range of activity 51 (12%),antibiotic administered with no indication 58 (13.65%)), Dosing problem(Regimen insufficient 103 (24.24%), Regimen excessive 150 (35.29%))

NR

Metronidazole [n = 110 (25.8%)] was used inappropriately which was followed by Cefuroxime + sulbactam [n = 63 (14.82%)]

An antibiotic stewardship program in which the Clinical pharmacist is an integral part along with well-framed institutional antibiotic guidelines must be implemented to assure appropriate antibiotic use.

8

[35]

India

There were 559 DRP causes found in all.  Of thesewere Drug choice problem(drug selection157(28.2%),drug use process [n = 127 (22.7%),no or insufficient drug therapy in spite of existing indication[n = 90 (16.1%)]), Dosing problem(dosage selection [n = 141 (25.0%)]) as causes of DRPs. 

Neonatal sepsis plus RDS 74 (17.3%), RDS plus RDS plus unconjugated hyperbilirubinemia 67 (15.7%), RDS plus 58 (13.6%), RDS plus pneumonia 53 (12.4%), RDS 43 (10.0%), RDS plus chronic heart disease 34 (7.9%), Unconjugated hyperbilirubinemia 31 (7.2%), Neonatal sepsis plus convulsion 28 (6.5%), pneumonia 18 (4.2), convulsion 12 (2.8%), Chronic heart disease

The most commonly prescribed drug class was antimicrobial agents [n = 1200(55.2%)], followed by respiratory agents [n = 378(17.4%)], with the primary medications in each class being gentamicin [n = 215(17.9%)] and caffeine [n = 127 (33.5%)].

Neonates admitted to the NICU frequently have DRPs.  Clinical pharmacists can be very helpful in detecting, preventing, and treating DRPs in newborns.

9

[36]

India

Adverse drug-event, followed by Drug choice problem(untreated indication anddrug selection,indication for drug-treatment not noticed),effect of treatment not optimal,  Dosing problem(dose selection,pharmacokinetic problem requiring dose adjustment and drug dose too high)

NR

Levofloxacin, simvastatin, paroxetine,

The participation of clinical pharmacists into multidisciplinary teams promotes the detection and solution of DRP. Polypharmacy, obesity, renal impairment and allergy are associated with a higher risk of DRP during admission.

10

[37]

Ethiopia

Half (60/121) of these drug-related issues were caused by treatment-effectiveness issues, with Drug choice problems(31/121, 26.3%), Dosing problem(19/121, 16.1%), and other unspecified but connected issues (19/121, 16.1%) following.

NR

NR

Drug-therapy-related issues were very common, and the medical ward had a high rate of acceptance of interventions that had significant effects on the economy, clinical practice, and organization.

11

[38]

Indonesia

Drug dose problem (No effect of drug treatment 8.68%, Effect of drug treatment not optimal 35.76%, Untreated symptoms or indication 22.22%,Unnecessary drug-treatment 17.36%, Inappropriate drug according to guidelines/formulary 2.95%, Inappropriate drug (within guidelines but otherwise contra-indicated) 3.22%,  No indication for the drug 13.17%, Inappropriate duplication of a therapeutic group or active ingredient 5.64%,  No or incomplete drug treatment despite an existing indication 20.16%,Too many drugs prescribed for an indication 1.34%), Adverse drug event (possibly) occurring 15.62%, , Drug drug interaction 13.44%, Dosing problem (Inappropriate drug form (for this patient) 0.53%, Drug dose too low 1.34%, Drug dose too high 1.88%, Dosage regimen not frequent enough 4.03%, Dosage regimen too frequent 0.53%, Duration of treatment too short 10.21%), Drug use process problem (Inappropriate timing of administration or dosing intervals 11.29%, Drug under-administered 3.49%, Drug not administered at all 2.15%, Wrong drug administered 0.26%,No or inappropriate outcome monitoring (incl. TDM) 0.26% )

NR

Antibiotic 23.1%, NSAID 12.5%, Steroids 7.6%, Antihyperglycemic6.6%, Gastroenterology drugs 6.3%, Antihypertension 5.6%, Antipyretics 5.3%, Antihistamines 3.6%, Antiemetics 2.6%, Antiepilepsy 2%, Antihyperlipidemic2%, Others12.2%, Untreated indication 10.6%,Total 100

The incidence of DRP in a patient is influenced by age, length of stay, and the number of medications taken; the incidence of DRP in a patient is influenced by gender in addition to age and medication.

12

[40]

Thailand

Dosing problem(Dosages that are too high (22.31%), too low (26.93%))and require additional medication therapy (27.09%), Drug choice problem(Ineffective medication (8.05%), unnecessary medication therapy (12.35%)),    Drug use process problem(2.15 percent non-adherence), Adverse drug events(1.12%)

Dyspnea and high blood pressure, neurotoxicity, hyperglycemia

Electrolytic calorie and water balance agents 179 items (13.82%), cardiovascular medications 171 items (13.20%), and antiinfective agents 307 items (23.71%)

The most frequent DRPs were the requirement for extra medication therapy and antimicrobial agent dosage modifications.  The ward's clinical pharmacists are proficient in both preventing and addressing DRPs.

 

13

[41]

India

Drug use process problem(Errors in prescription [92 (45.1%)], documentation [69 (33.82%)], and administration [43 (21.08%)] )were the next most common.

NR

Sodium chloride [11 (5.47%)], glimepiride [10 (4.97%)], insulin [19 (9.45%)], magnesium sulfate [9 (4.48%)], and potassium chloride were implicated in 26 (12.94%) of MEs.  Twenty-eight percent (58) of the errors were related to medications used in the cardiovascular system.  Blood and organs that form blood [30 (14.92%)], medications under the nervous system [33 (16.42%)], and IV fluids [5 (2.49%)] were the least frequently used HAMs in error.

 

Even though error prevention has advanced significantly, the objective of making HAM errors "never" occur has not been met.  Therefore, a clinical pharmacist's active monitoring could help the medical staff advance patient care.

14

[42]

Iran

Drug-drug interactions (36.26%) and Drug choice problem(126 prescriptions, 29.86%)

Pneumonia (35.6%), gastroenteritis problems (10.8%), and trauma (9.6%). diabetes mellitus (DM), glucose-6-phosphate dehydrogenase (G6PD) deficiency, and central nervous system (CNS) disorders

Antibiotics (53.47%), anticonvulsants (18.56%), and proton pump inhibitors (PPIs) (20.06%).

The incidence of DRPs is high among patients admitted to PICUs.  It is crucial to think about the best possible dosage modification, especially for young patients with compromised kidney function.

15

[43]

India

Drug choice problem(Duplication of a therapeutic group or active ingredient (1.5%), no clear indication for drug use (4.6%),noprescription but clear indication (3.8%)), Dosing problem(inappropriate drug form (6.1%), Drug drug interaction(4.1%)

Foot or ankle swelling, hypotension (3.3%), hypoglycemia (3.2%), mild rash or itching (1.5%), extreme sleepiness (1.4%), and skin rashes (1.0%)

Insulin + Emeril accounted for the majority of drug interactions (226; 11.8%), followed by Emeril + PCM + Diclofenac (111; 5.8%).

Clinical pharmacists play a vital role in reducing issues related to drugs.  More focus should be placed on patient counseling and follow-up in particular.

16

[44]

India

Out of a total of 24,572 medication orders, 2,624 had prescription errors

The central nervous system (27), gastrointestinal (10), cardiovascular (9), musculoskeletal (9), endocrinological involvement (4), infections (12), renal (12), respiratory involvement (37), and poisoning (15) come next.

89 (0.4%; 95% CI 0.3–0.4), cardiovascular 82 (0.3%; 95% CI 0.3–0.4), antihypertensives 55 (0.2%; 95% CI 0.2–0.3), general care and nutrition 1,367 (5.6%; 95% CI 5.3–5.8).

10.7% of MPEs occurred in the tertiary care hospital's medical intensive care unit, with 3.52% of those errors being considered severe.

17

[45]

United Arab Emirates

Drug choice problem(61%, n = 503), dosing problem(22%, n = 225)

NR

Antimicrobial agents

The study highlights the importance of CP in the intensivecare unit, addressing DRPs and improving patient care in general.  It also draws attention to how pharmacist interventions may enhance patient survival results.  This emphasizes how crucial it is to introduce CP services in ICUs throughout the United Arab Emirates.

18

[46]

Thailand

Dosing problem(excessive dosage (27.7%)), Drug choice problem(ineffective medication (17.2%), need for further medication (15.3%), needless medication (14.6%),) adverse drug event (9.7%), andDrug use process problem(1.2%).

Sepsis or septic shock, Hemodynamic unstable, Hemorrhagic or hypovolemic shock, Postcardiac arrest, Status epilepticus, Drug overdose

Intravenous phenytoin, amiodarone, propofol, midazolam, vancomycin, acyclovir, ganciclovir, amikacin, ophthalmic lubricants, proton-pump inhibitors (PPIs), trimethoprim and sulfamethoxazole, meropenem, levofloxacin, fluconazole, and colistin

In the tertiary university hospital's medical intensive care unit, the most common drug-related issue found during medication care interventions is an excessive dosage..

19

[47]

China

Drug Choice problem(124; 44.1%), Dosing problemC3(92;32.7%)

Cerebrovascular disease, hypertension, diabetes, infectious diseases, and atrial fibrillation

Traditional Chinese Medicine (85.2%), antihyperlipidemic drugs (86.4%), antiplatelet drugs (81.9%), antihypertensive drugs (71.0%), and drugs for the digestive system (46.2%)

Clinical pharmacists can successfully minimize and prevent DRPs to maximize medication therapy. DRPs are a common occurrence in the neurology unit in China, and they are the main reason for drug and dose selection.

20

[48]

Ethiopia

Drug use process problem(17.22%), Drug choice problem92 (27.79%), and Dosing problem(16.92%)

NR

Diclofenac 31 (14.42%), ceftriaxone 61 (27.37%), and cimetidine 32 (14.88%)

It was discovered that a significant number of patients admitted to the study settings' medical wards had drug therapy issues.  In order to address the DTPs in this area, clinical pharmacy services ought to be implemented in hospital.

Note: NR = Not reported. Blank cells were completed using these standardized abbreviation to improve data clarity. DRP categories were standardized according to the Pharmaceutical Care Network Europe (PCNE) Classification V9.1. Original study terminology was harmonized for consistency.

 

 

DISCUSSION

DRPs continue to be a major and complex issue in hospital settings for a variety of patient populations, including critically ill patients, adults, and neonates, according to an analysis of 20 recent studies. Unsuitable drug or dose selection, ADRs, left untreated indications, DDIs, polypharmacy, and failure to adhere are among the most frequently reported DRPs.These results demonstrate the universal applicability and similarity of DRP patterns across geographic locations and hospital departments.

Antimicrobials, cardiovascular agents, antidiabetics, and CNS medications were among the drug classes most commonly linked to DRPs.For instance, serious side effects like hypoglycemia, thrombocytopenia, and nephrotoxicity have been linked to medications like insulin, glimepiride, linezolid, piperacillin–tazobactam, metronidazole, and calcium channel blockers [28-32]. Therapeutic risks were further increased by the misuse of combination therapies, such as cefuroxime-sulbactam, metformin-based fixed-dose combinations, and insufficient PPI prescriptions [28, 33-34].

Inadequate care, even when clear treatment indications were present, was a recurring contributor to DRPs, particularly among neonates with sepsis and respiratory distress syndrome (RDS) [32,35]. Inappropriate antibiotic use was another critical concern, as it increases the risk of antimicrobial resistance and healthcare costs, with common issues including prescriptions without indication and overlapping spectrum combinations [31,35-36].

The occurrence of DRPs was further driven by multiple system-level and patient-related factors such as advanced age, polypharmacy, prolonged hospitalisation, comorbidities, low birth weight, lack of vaccination, cesarean delivery, smoking, alcohol use, and male sex [28-29,32-33,35-39]. These findings underscore that DRPs extend beyond medication errors alone, reflecting the interplay of medical complexity and sociodemographic determinants. Establishing comprehensive risk assessment frameworks is therefore vital to guide targeted interventions and improve patient safety. Interestingly, all of the studies reported a high success rate for the intervention.  Some studies found that up to 99% of DRPs were resolved by interventions like dose modification, drug termination, addition of needed therapy, and formulation modifications [35,38,40].  But because of complicated clinical circumstances, a portion of DRPs remained unresolved, underscoring the shortcomings of reactive approaches and the necessity of proactive ones like therapeutic drug monitoring and medication reconciliation.

MEs were also identified as a significant contributor to DRPs, particularly during the prescribing, documentation, and administration stages.  These errors were linked to a number of factors, including duty shifts, peak workload, staff fatigue, and interruptions during care transitions [41].  These systemic flaws are especially noticeable in hospitals with limited resources, where documentation procedures and pharmacovigilance practices may be lacking.

The studies also support the critical role that interprofessional collaboration and clinical pharmacists play in detecting and fixing DRPs [32,37,42].  It has been demonstrated that incorporating computerised decision support systems, routine monitoring, and structured medication reviews improves results.  Avoidable DRPs can also be reduced by enhancing access to updated treatment protocols and putting in place educational interventions for prescribers.

CONCLUSION

This systematic review demonstrates that DRPs continue to be a recurring and avoidable issue in a variety of hospital settings.  Although DDIs, ADRs, and improper prescribing were the most common, polypharmacy, comorbidities, and deficiencies in clinical assessment were frequently the root causes.  Significantly, research indicates that proactive strategies like pharmacist-led interventions, medication reconciliation, and therapeutic drug monitoring can resolve up to 99% of identified DRPs, proving their clinical value.

To detect and prevent DRPs in real time, healthcare systems should prioritise integrating clinical pharmacists into multidisciplinary teams, strengthening pharmacovigilance infrastructure, and implementing digital decision-support tools.  Future studies should also concentrate on measuring the financial cost of DRPs and assessing the long-term effects of intervention models in low- and middle-income environments.  Improving medication safety, maximising treatment results, and attaining safer, more sustainable healthcare delivery will all depend on strengthening these tactics.

ACKNOWLEDGEMENT

I express my sincere gratitude to PES's Modern College of Pharmacy Nigdi, Pune, for lending me the resources and facilities required to conduct this study. I really appreciate the Department of Pharm D for their assistance and expertise.

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