Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Lasmiditan
Drug ID BADD_D02562
Description Lasmiditan is an oral medication used in the termination of migraine headaches that was first approved for use in the United States in October 2019.[L9338,L9356] Traditionally, the triptan class of anti-migraine medications (e.g. [sumatriptan]) have seen preferential use in the acute treatment of migraines due to their relatively favourable efficacy and safety. Their use is not devoid of concerns, however, and their vasoconstrictive activity can lead to blood pressure lability and other cardiovascular side effects - for this reason, these medications are less suitable for use in patients with pre-existing cardiovascular disorders.[A187316] Triptans abort migraines via action at several serotonin receptors, including 5-HT1D and 5-HT1B receptors, and activity at the 5-HT1B receptor has been specifically implicated in their vasoconstrictive activity.[A187316,A187322] Lasmiditan, in contrast, is a highly selective agonist of 5-HT1F receptors, carrying virtually no affinity for other receptors which appear to be largely responsible for the adverse effect profile of its predecessors - in other words, lasmiditan’s selectivity allows for the successful termination of migraines without causing vasoconstriction.[A187322,A187319] Selectivity for 5-HT1F, a lack of vasoconstrictive activity, and the ability to terminate migraines through neuronal inhibition has resulted in the creation of a new class of anti-migraine medications in which lasmiditan is the first and only member: the neurally-acting anti-migraine medications (NAAMAs).[A187322,A187307]
Indications and Usage Lasmiditan is indicated for the acute treatment of migraine with or without aura in adults.[L9338]
Marketing Status approved; investigational
ATC Code N02CC08
DrugBank ID DB11732
KEGG ID D10338
MeSH ID C554777
PubChem ID 11610526
TTD Drug ID D01NQM
NDC Product Code 0002-4312; 0002-4491; 0110-4491; 0110-4312
UNII 760I9WM792
Synonyms lasmiditan | 2,4,6-trifluoro-N-(6-((1-methylpiperidin-4-yl)carbonyl)pyridin-2yl)benzamide | Reyvow | lasmiditan hydrochloride | COL-144 | LY573144
Chemical Information
Molecular Formula C19H18F3N3O2
CAS Registry Number 439239-90-4
SMILES CN1CCC(CC1)C(=O)C2=NC(=CC=C2)NC(=O)C3=C(C=C(C=C3F)F)F
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abnormal dreams19.02.03.001; 17.15.02.0010.000906%-
Anxiety19.06.02.0020.000793%
Burning sensation17.02.06.001; 08.01.09.0290.000340%-
Chest discomfort22.12.02.002; 08.01.08.019; 02.02.02.0090.000566%-
Discomfort08.01.08.0030.000566%-
Disorientation19.13.01.002; 17.02.05.0150.000340%-
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.0030.013932%
Drug ineffective08.06.01.0060.005581%-
Euphoric mood19.04.02.0060.001811%
Fatigue08.01.01.0020.003623%
Feeling abnormal08.01.09.0140.007992%-
Feeling drunk08.01.09.0150.000679%-
Feeling jittery08.01.09.0160.000340%-
Formication17.02.06.018; 19.10.04.0020.000226%-
Gait disturbance15.03.05.013; 17.02.05.016; 08.01.02.0020.000486%
Hallucination19.10.04.0030.002830%
Hallucination, visual19.10.04.0070.000486%-
Head discomfort17.02.05.0270.000226%-
Hypersomnia19.02.05.001; 17.15.01.0010.000679%
Hypoaesthesia23.03.03.081; 17.02.06.0230.000939%-
Insomnia19.02.01.002; 17.15.03.0020.001019%
Lethargy19.04.04.004; 17.02.04.003; 08.01.01.0080.000226%
Malaise08.01.01.0030.001019%
Mental impairment19.21.02.003; 17.03.03.0020.000226%-
Migraine24.03.05.003; 17.14.02.0010.001392%-
Muscular weakness17.05.03.005; 15.05.06.0010.000486%
Nausea07.01.07.0010.003689%
Nightmare19.02.03.0030.000453%-
Palpitations02.11.04.0120.000566%
Panic attack19.06.04.0010.000566%-
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