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magnesium

L-type Ca2+ channel blocker, RyR2 inhibitor · Antiarrhythmic

L-type Ca2+ channel blocker, RyR2 inhibitorAntiarrhythmicATC A12CC02
CDSCO approvedATC A12CC02
EXCRETION
not curated
INTERACTIONS
6 major
SEVERE in our sources
PREGNANCY
not curated
Top interactionssee all 9
  • BictegravirSevereDatabaseDDInter
  • DolutegravirSevereDatabaseDDInter
  • ErdafitinibSevereDatabaseDDInter
  • PatiromerSevereDatabaseDDInter

Mechanism

Magnesium is effective by blocking L-type Ca2+ currents responsible for the triggered upstroke arising from EADs. It is also an inhibitor of RyR2 Ca2+ release channels.

Indications

Preventing recurrent episodes of torsades de pointes (even with normal serum Mg2+)Arrhythmias related to digitalis intoxication

Dosing

Adult
1–2 g MgSO4 (IV)

Pharmacokinetics

Protein binding
Not specified

Drug interactions

Bictegravir
Severe
Database

Clinical effect not specified

Source: DDInter

Dolutegravir
Severe
Database

Clinical effect not specified

Source: DDInter

Erdafitinib
Severe
Database

Clinical effect not specified

Source: DDInter

Patiromer
Severe
Database

Clinical effect not specified

Source: DDInter

Selpercatinib
Severe
Database

Clinical effect not specified

Source: DDInter

Tolevamer
Severe
Database

Clinical effect not specified

Source: DDInter

Tetracyclines
Moderate
Textbook

Poor absorption of tetracycline.

Avoid concurrent ingestion. Dairy products, antacids, aluminum hydroxide gels; calcium, magnesium, iron, or zinc salts; bismuth subsalicylate; and dietary iron and zinc supplements can interfere with absorption of tetracyclines. Omadacycline specifically requires administration on an empty stomach, at least 4 hours after and 2 hours before food consumption. Food, including dairy products, does not interfere with absorption of doxycycline and minocycline but significantly impairs the absorption of omadacycline.

Source: G&G 14e · p1181

Elvitegravir
Moderate
Database

Reduced bioavailability of elvitegravir.

Subject to similar restrictions as raltegravir (take 6h before or 2h after).

Source: DDInter

Gabapentin
Moderate
Database

Antacids reduce gabapentin bioavailability by ~20% through chelation and/or reduced gastric residence time.

Separate administration by at least 2 hours. Give gabapentin at least 2 hours after antacid dose.

Source: Kimi deep-research + Cla

3 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

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Sources: Goodman & Gilman 14e·Verified: 2026-05-10 · House clinical team