Anticonvulsants Flashcards
Lamotrigine (Lamictal) Dosing
Normal:
25mg QD x14, 50mg QD x14, 100mg QD x7, 200mg QD
Inducer:
50mg QD x14, 100mg QD x14, 200mg QD x7, 400mg QD
Inhibitor:
25mg QOD x14, 25mg QD x14, 50mg QD x7, 100mg QD
Lamotrigine (Lamictal) Adverse Effects
Stevens-Johnson Syndrome
Lamotrigine (Lamictal) Monitoring/Clinical
OC interaction: decrease effectiveness of OC’s and decrease lamotrigine conc.
Levetiracetam (Keppra) Dosing
Renal dosing adjustment needed
Levetiracetam (Keppra) Adverse Effects
Behavioral abnormalities, psychosis, suicidal thoughts/behaviors, unusual mood changes or worsening of depression - most commonly in younger patients
Valproate (Depakote, Depakene, Depacon) Dosing
Monitor serum concentrations: 50-125 mcg/ml
Valproate (Depakote, Depakene, Depacon) Adverse Effects
Hyperammonemia, thrombocytopenia, N/V, weight gain, alopecia, PCOS
Valproate (Depakote, Depakene, Depacon) Monitoring/Clinical
Pregnancy D
Monitor: CBC with platelets, LFTs, serum conc.
Zonisamide (Zonegran) Adverse Effects
CI’d in sulfa hypersensitivity, metabolic acidosis, renal calculi
Zonisamide (Zonegran) Monitoring/Clinical
Metabolized via glucuronidation (UDP-GT)
Clobazam (Onfi) C-IV Adverse Effects
Withdrawal symptoms
Clobazam (Onfi) C-IV Monitoring/Clinical
3A4 substrate (major), inducer (weak), may decrease efficacy of oral contraceptives
Clonazepam (Klonopin) C-IV Adverse Effects
Anterograde amnesia, paradoxical reactions, withdrawal symptoms
Clonazepam (Klonopin) C-IV Monitoring/Clinical
3A4 substrate (major), Pregnancy D
Carbamazepine (Tegretol, Carbatrol, Epitol) Dosing
Monitor serum concentrations: 4-12 mcg/ml
Carbamazepine (Tegretol, Carbatrol, Epitol) Adverse Effects
Boxed warning: Stevens-Johnson Syndrome (Asians who are HLA-B1502 +), DRESS (Northern European HLA-A3101 +), aplastic anemia, hyponatremia
Carbamazepine (Tegretol, Carbatrol, Epitol) Monitoring/Clinical
Pregnancy D, 3A4 substrate (major), strong inducers of 1A3, 2B6, 2C8, 2C9, 2C19, 3A4
Monitoring: CBC with platelets, electrolytes, may autoinduce own metabolism for several weeks after initiation and dose increases
Eslicarbazepine Acetate (Aptiom) Adverse Effects
Stevens-Johnson Syndrome, hyponatremia, same HLA-B/HLA-A as carbamazepine
Eslicarbazepine Acetate (Aptiom) Monitoring/Clinical
Rapidly metabolized to active metabolite eslicarbazepine, active metabolite of oxcarbazepine, 2C19 inhibitor (moderate)
Monitoring: electrolytes
Ezobagine (Potiga) C-V Dosing
Renal dosing: CrCl less than 50ml/min: 600mg
Ezobagine (Potiga) C-V Adverse Effects
Boxed warning: retinal abnormalities, may progress to vision loss
Warnings: urinary retention, grey-blue/brown skin discoloration (sign of toxicity), QTc prolongation, memory impairment, hallucinations
Ezobagine (Potiga) C-V Monitoring/Clinical
Baseline ophthalmic exam, repeat every 6 months
Felbamate (Felbatol) Adverse Effects
Boxed warning: aplastic anemia, hepatic failure
Felbamate (Felbatol) Monitoring/Clinical
MUST monitor LFT’s at baseline and frequently after, D/C if evidence of bone marrow suppression
Gabapentin (Nuerontin, Gralise, Fanatrex) Dosing
Renal dosing: CrCl 30-60 ml/min: 600-1800 mg/day
Not recommended CrCl less than 30 ml/min
Gabapentin (Nuerontin, Gralise, Fanatrex) Adverse Effects
Somnolence, peripheral edema
Gabapentin (Nuerontin, Gralise, Fanatrex) Monitoring/Clinical
Renal clearance: 100%
Monitor renal function at baseline and routinely
Lacosamide (Vimpat) Adverse Effects
Use with caution in patients with cardiac conduction abnormalities, prolongs PR interval, dermatological reactions, visual disturbances, idiosyncratic reactions: hepatic impairment, 1st degree AV block
Lacosamide (Vimpat) Monitoring/Clinical
2C19 substrate and inhibitor (major)
Oxcarbazepine (Trileptal, Oxtellar) Dosing
Oxcarbazepine is 1.5 times the dose of carbamazepine if converting
Oxcarbazepine (Trileptal, Oxtellar) Adverse Effects
Same HLA-B/HLA-A as carbamazepine, hyponatremia
Oxcarbazepine (Trileptal, Oxtellar) Monitoring/Clinical
3A4/5 substrate/inducer (major/strong), 2C19 inhibitor (moderate)
Monitoring: electrolytes
Perampanel (Fycompa) C-III Adverse Effects
Boxed warning: dose-related serious and/or life threatening neuropsychiatric events, use with caution in patients with pre-existing behavioral problems or psychosis, gait disturbances, somnolence
Perampanel (Fycompa) C-III Monitoring/Clinical
3A4/5 substrate (major)
Phenobarbital C-IV Dosing
Monitor serum concentrations 15-40 mcg/ml
Phenobarbital C-IV Adverse Effects
Somnolence, confusion, cognitive impairment, impaired calcium metabolism
Phenobarbital C-IV Monitoring/Clinical
Pregnancy D, 2C9 substrate (major), 1A2, 2C, 3A, and UGT inducer (strong)
Phenytoin (Dilantin) Dosing
Fosphenytoin (Cerebyx) Dosing
Monitor serum concentrations 10-20 mpg/ml (phenytoin), conversion from fosphenytoin to phenytoin occurs 0.5-1 hour post-dose
Phenytoin (Dilantin) Adverse Effects
Fosphenytoin (Cerebyx) Adverse Effects
Fospheytoin IV: hypotension, arrhythmias
Phenytoin IV: arrhythmias, hypotension, purple glove syndrome
CI’d with sinus bradycardia or 2nd/3rd degree heart block
Decreased BMD, dermatological reactions, nystagmus, ataxia, double vision, hepatotoxicity, hirsutism, gingival hyperplasia, cardiac arrhythmias, Stevens-Johnson Syndrome, alteration of Vit D metabolism, osteoporosis
Phenytoin (Dilantin) Monitoring/Clinical
Fosphenytoin (Cerebyx) Monitoring/Clinical
Pregnancy D, 2C9/2C19 substrate (major), 1A2, 2C19, 3A4, and UGT inducer (strong), serum conc (obtain albumin with same blood draw)
Pregabalin (Lyrica) C-V Dosing
Renal dosing adjustment needed
Pregabalin (Lyrica) C-V Adverse Effects
Angioedema, peripheral edema, PR interval prolongation
Pregabalin (Lyrica) C-V Monitoring/Clinical
Renal clearance 100%
Primidone (Mysoline) Adverse Effects
Metabolized to phenobarbital, same side effects as phenobarbital
Primidone (Mysoline) Monitoring/Clinical
Pregnancy D
Rufinamide (Banzel) Dosing
Indicated for Lennox-Gastaut Refractory Seizures
Rufinamide (Banzel) Adverse Effects
CI’d if familial short QT syndrome
DRESS, Stevens-Johnson Syndrome
Tiagabine (Gabitril) Dosing
Special dosing for concomitant enzyme inducing drugs and concomitant valproate therapy
Monitor serum concentrations 0.02-0.2 mcg/ml
Tiagabine (Gabitril) Adverse Effects
Use with caution off-label for patient without seizure disorder and with hectic disease - may trigger seizures, cognitive impairment
Tiagabine (Gabitril) Monitoring/Clinical
3A4 substrate (major)
Topiramate (Topamax) Dosing
50% reduced dose with CrCl less than 70 ml/min
Topiramate (Topamax) Adverse Effects
Use with caution in patients with nephrolithiasis, renal impairment, hepatic disease
CNS depression, metabolic acidosis, oligohydrosis/hyperthermia, acute myopia, secondary angle-closure glaucoma, nephrolithiasis, visual field defects, cognitive impairment, hyperchloremic non-anion gap metabolic acidosis
Topiramate (Topamax) Monitoring/Clinical
Pregnancy D, 2C19 inhibitor (moderate), 3A4 substrate/inducer (moderate-strong, dose dependent)
Monitoring: basic metabolic profile, urinalysis every 3-6 months
Vigabatrin (Sabril) Dosing
Indicated for Refractory Seizures, dosing needs renally adjusted
Vigabatrin (Sabril) Adverse Effects
CI’d in patients with other risk factors for irreversible vision loss
Boxed warning for vision loss
Peripheral neuropathy, depression, weight gain, insomnia, permanent loss of peripheral vision
Vigabatrin (Sabril) Monitoring/Clinical
SCr, vision assessment at baseline and every 3-6 months
Ethosuximide (Zarontin) Dosing
Indicated for Absence Seizures
Ethosuximide (Zarontin) Adverse Effects
Avoid in renal/hepatic dysfunction, SLE, Stevens-Johnson Syndrome, leukopenia, eosinophilia, psychiatric and sleep disturbances, aggression, hiccups