Drug-induced aseptic meningitis: 329 cases from the French pharmacovigilance database analysis

Kevin Bihan1, Nicolas Weiss2,3, Hélène Théophile4

  • 1Regional Pharmacovigilance Center, Department of Pharmacology, Pitié-Salpêtrière Hospital, Paris, France.

Abstract

Insights

Drug-induced aseptic meningitis (DIAM) is rare but usually resolves fully. Intravenous immunoglobulin, NSAIDs, vaccines, and antimicrobials are common culprits, highlighting the need for pharmacovigilance.

Area of Science:

  • Pharmacovigilance
  • Clinical Pharmacology
  • Neurology

Background:

  • Drug-induced aseptic meningitis (DIAM) is an understudied iatrogenic condition.
  • Characterizing DIAM and identifying causative agents is crucial for patient safety.

Purpose of the Study:

  • To characterize drug-induced aseptic meningitis (DIAM).
  • To identify drugs suspected of causing aseptic meningitis.

Main Methods:

  • Analysis of the French Pharmacovigilance Database (1985-2017).
  • Application of the French imputability method for case assessment.
  • Detailed analysis of well-documented DIAM cases.

Main Results:

  • 329 DIAM cases and 429 suspected drugs identified.
  • Common drug classes included intravenous polyvalent immunoglobulin, NSAIDs, vaccines, and antimicrobials.
  • Most cases (96%) showed favorable outcomes with full recovery.

Conclusions:

  • Intravenous polyvalent immunoglobulin, NSAIDs, vaccines, and antimicrobials are frequently implicated in DIAM.
  • Further research into DIAM pathophysiology is needed.
  • Pharmacovigilance databases are vital for identifying DIAM signals and aiding clinical understanding.

Related Concept Videos

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...
1.6K
Cranial and Spinal Meninges01:19

Cranial and Spinal Meninges

The cranial and spinal meninges are complex protective structures surrounding the central nervous system (CNS), consisting of the brain and spinal cord. These meninges consist of the dura mater, the arachnoid mater, and the pia mater. They protect the CNS, provide structural support, and aid in circulating cerebrospinal fluid (CSF).
Cranial Meninges
These meningeal layers cover the cranium. The dura mater is the outermost layer of cranial meninges. It is a thick and durable membrane of dense...
3.7K
Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
183
Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
384
Bioequivalence of Drugs: Drugs with Multiple Indications01:09

Bioequivalence of Drugs: Drugs with Multiple Indications

The concept of therapeutic equivalence (TE) in drugs with multiple indications is complex. A generic drug may be therapeutically equivalent to a brand-name product for one specific indication, but this doesn't necessarily mean it's equivalent for all other indications. Evidence of TE in one patient group and bioequivalence shown in healthy volunteers can support—but not confirm—TE for other indications. However, definitive proof requires individual clinical studies for each...
154
FDA Approved Drugs: Changes to Approved Drugs01:26

FDA Approved Drugs: Changes to Approved Drugs

Post-approval, manufacturers may modify an approved new or generic drug product. Such modifications can encompass alterations in the Active Pharmaceutical Ingredient (API), manufacturing process, formulation, batch size, manufacturing site, and container closure system (FDA Guidance for Industry, April 2004). Often, a drug product may undergo multiple changes.These modifications require careful evaluation to determine their potential impact on the drug product's identity, strength, quality,...
246