India's ban on antimicrobial fixed-dose combinations: winning the battle, losing the war?

Giorgia Sulis1, Richeek Pradhan1, Anita Kotwani2

  • 1Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC, Canada.

Abstract

Insights

India

Area of Science:

  • Pharmacology and Public Health
  • Antimicrobial Resistance Studies

Background:

  • India, a major market for antimicrobial fixed-dose combinations (FDCs), banned specific FDCs in September 2018.
  • The ban aimed to address concerns related to antimicrobial drug usage and resistance.

Purpose of the Study:

  • To evaluate the impact of the government ban on the sales volume of antimicrobial fixed-dose combinations (FDCs).

Main Methods:

  • Analysis of monthly private sector drug sales data from IQVIA for 14 banned antimicrobial FDCs.
  • Descriptive analysis of sales trends for banned and non-banned FDCs from January 2018 to December 2019.

Main Results:

  • A 75% decline in cumulative sales volume for banned antimicrobial FDCs was observed.
  • Sales of similar drug-class combinations and non-banned formulations increased post-ban.
  • Availability of banned combinations persisted through products with added non-antimicrobial components.

Conclusions:

  • Despite a decrease in banned FDC sales, the ban's effectiveness was limited.
  • Implementation failures and market substitutions, including congeners and modified formulations, counteracted the ban's impact.

Related Concept Videos

Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
5.0K
Drug Regulation01:25

Drug Regulation

Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
1.9K
Dosage Regimen: Fixed Dose01:01

Dosage Regimen: Fixed Dose

Fixed-dose regimens are a common approach to administer drugs to achieve and maintain desired levels of the drug in the body. In this dosing strategy, a specific amount of medication is given at regular intervals, often multiple times a day, to ensure a consistent drug concentration in the bloodstream.
Fixed-dose regimens can be used for various routes of administration, including intravenous (IV) injections and oral medications. For IV administration, a predetermined amount of the drug is...
2.0K
Antibiotic Selection00:57

Antibiotic Selection

Overview
55.6K
Development of Antibiotic Resistance01:30

Development of Antibiotic Resistance

Antibiotic resistance is a major public health concern that arises when bacteria evolve mechanisms to withstand the effects of antibiotic treatments. This resistance can be intrinsic, acquired through genetic mutations, or transferred between bacteria via horizontal gene transfer. The development of antibiotic resistance poses significant challenges in treating bacterial infections and necessitates ongoing research to develop new therapeutic strategies.Intrinsic resistance occurs when bacterial...
273
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
1.0K