Their antimuscarinic action is likely to intensify the toxicity of atropine poisoning.
Phenothiazines should not be used in atropine poisoning.
Source: G&G 14e · p218
Antipsychotic
Not yet extracted
Their antimuscarinic action is likely to intensify the toxicity of atropine poisoning.
Phenothiazines should not be used in atropine poisoning.
Source: G&G 14e · p218
Increased risk of cardiac conduction defects.
Source: KDT 7e · p816-835
Reverse the therapeutic effect of levodopa.
Avoid co-administration.
Source: KDT 7e · p429
Partial antagonism of overdose symptoms and coma; however, it may worsen the fall in BP and arrhythmias.
Use is risky.
Source: KDT 7e · p110
Decreased absorption of phenothiazines.
Stagger administration of antacids and phenothiazines by 2 hours.
Source: KDT 7e · p656
Increased anticholinergic side effects (dry mouth, altered bowel movement, urinary hesitancy, blurring of vision).
Monitor for increased anticholinergic effects.
Source: KDT 7e
Delirium, convulsions, and other excitatory effects during recovery from intravenous anaesthetics.
Excitatory effects are generally suppressed by opioids.
Source: KDT 7e · p385
Reduced glucose-lowering effect of sulfonylureas.
Source: G&G 14e · p1034
Additive anticholinergic effects; phenothiazines have intrinsic anticholinergic activity
Monitor for anticholinergic toxicity
Source: Kimi deep-research + Cla
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: KD Tripathi 7e·Verified: 2026-05-10 · House clinical team