Lithium (0.8-1.2 mmol/L)

Lamotrigine

Valproate, CI: G

Carbamazepine

For Bipolar Disorder (3/7, 4 or 7 dys)

Lithium Carbamazepine Oxcarbazepine Lamotrigine
Indications Bipolar disorder, depression Bipolar disorder Bipolar disorder Bipolar disorder
Approval in Youth No No No No
Pharmacokinetics Not metabolised, excreted by kidneys Phase II 90% (glucuronidation), Phase I 10% Phase I CYP3A4, 2C19 (autoinducing) Minimal P450 interactions, does not autoinduce, more favourable side effect profile
Monitoring Lithium levels, kidney function, thyroid function Epival levels, albumin level, liver function Carbamazepine level, albumin level, liver function Oxcarbazepine metabolite level, albumin level, liver function
Side Effects Tremors, acne, thyroid disorders, hypercalcemia GI issues, weight gain, hair loss, tremor, PCOS, thrombocytopenia, hair loss, encephalopathy, cognitive dulling[2] Cognitive dulling, diplopia, nystagmus, vertigo, hyponatremia Cognitive dulling, hyponatremia
Adverse Reactions Renal impairment, nephrotoxicity Pancreatitis, hepatoxcitity Agranulocytosis, aplastic anemia, hepatotoxicity, Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) Agranulocytosis, aplastic anemia, hepatotoxicity, Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN)
Teratogen Ebstein's anomaly (cardiac) Neural tube defects Neural tube defects, cleft lip Neural tube defects, cleft lip
Drug-Drug Interactions ACE inhibitors, angiotensin II receptor antagonists (ARBs), thiazide diuretics, NSAIDs, COX-2 Inhibitors The combination of VPA with lamotrigine can cause significant and dangerous increases of lamotrigine, due to inhibition of the glucuronidation. Potent CYP interactions with many drugs. Many!!!
Notes The gold standard treatment for bipolar disorder. In bipolar disorder, may be better for those with comorbid substance use, or traumatic brain injuries In bipolar disorder, may be better for those with comorbid substance use, substance use disorder, or a negative family history of bipolar disorder. Similar to carbamazepine, but has several advantages, including no autoinduction, and much less CYP P450 enzyme interactions