Pharmacogenetics by drug class

Every therapeutic class has its own pharmacogenetic story. Choose a class to see which medications have published genetic guidelines and which genes are involved.

Chemotherapy agents
Pharmacogenetic testing in oncology is the most well-established and consequential part of clinical pharmacogenetics. Several chemotherapy drugs have mandatory or strongly recommended pre-treatment genetic testing because the toxicity difference between …
Pain medications
Pharmacogenetics affects pain management on two fronts: how opioids are activated (or not) and how NSAIDs are cleared. The CYP2D6 gene is central to the opioid story because it converts …
Tricyclic antidepressants
Tricyclic antidepressants (TCAs) predate SSRIs and remain in use for depression, chronic pain, migraine prevention, and some sleep conditions. Nearly all TCAs are cleared by CYP2D6 and CYP2C19, often in …
Antipsychotics
Antipsychotics treat schizophrenia, bipolar disorder, severe depression (as augmentation), and several other conditions. Modern antipsychotics mostly clear through CYP2D6 and CYP3A4, with smaller contributions from CYP1A2. Aripiprazole, brexpiprazole, iloperidone, and …
Statins
Statins are the mainstay of cholesterol management and cardiovascular disease prevention. They share a class-wide pharmacogenetic story: the SLCO1B1 transporter moves statins from blood into liver cells where they work. …
SSRI antidepressants
SSRIs (selective serotonin reuptake inhibitors) are the most-prescribed antidepressant class, used for major depression, anxiety disorders, PTSD, OCD, and premenstrual dysphoric disorder. Most SSRIs are cleared by CYP2C19, CYP2D6, or …
Anticonvulsants
Anticonvulsants treat epilepsy, bipolar disorder, trigeminal neuralgia, and neuropathic pain. The most consequential pharmacogenetic signal in this class is not about metabolism but about hypersensitivity: HLA-B*15:02 carriers have a dramatically …
Proton pump inhibitors
Proton pump inhibitors (PPIs) are among the most prescribed drugs globally, used for GERD, peptic ulcer disease, and Helicobacter pylori eradication. Most PPIs are metabolized predominantly by CYP2C19. Rapid and …
Immunosuppressants
Immunosuppressants prevent organ rejection after transplant and control autoimmune conditions like lupus, inflammatory bowel disease, and rheumatoid arthritis. Pharmacogenetics is unusually critical in this class because the drugs have narrow …
Antiemetics
Antiemetics prevent nausea and vomiting in contexts like chemotherapy, post-operative recovery, and migraine. The clinically relevant pharmacogenetic signal in this class is CYP2D6 for ondansetron and its relatives. CYP2D6 ultrarapid …
Antivirals
The biggest pharmacogenetic story in antivirals is HLA-B*57:01 screening before abacavir, which essentially eliminated a previously common and sometimes fatal hypersensitivity reaction. This is one of the cleanest clinical wins …
Movement disorder medications
Medications for involuntary movement disorders (tardive dyskinesia, Huntington's disease chorea) work by depleting dopamine at nerve terminals. Several are metabolized by CYP2D6, which means poor metabolizers are at higher risk …
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