Article Author:
Aaron Cross
Article Author:
Omar Viswanath
Article Editor:
Andrew Sherman
12/5/2020 8:28:24 AM
For CME on this topic:
Pregabalin CME
PubMed Link:


Pregabalin has approval from the United States Food and Drug Administration (FDA) to treat neuropathic pain associated with diabetic peripheral neuropathy, spinal cord injury, and postherpetic neuralgia. Pregabalin is FDA-approved for the treatment of fibromyalgia. Pregabalin is also FDA approved as adjunctive therapy for partial-onset seizures in adults with epilepsy. Off-label uses include generalized anxiety disorder, social anxiety disorder, bipolar disorder, insomnia, and chronic pain conditions not otherwise approved by the FDA. There is significant disagreement regarding the effectiveness of pregabalin for the psychiatric disorders listed above.[1][2][3][4]

Mechanism of Action

Pregabalin is structurally similar to the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). It has been modified to be a lipophilic analog to enhance diffusion across the blood-brain barrier. However, pregabalin does not directly bind to GABA-A or GABA-B receptors. Additionally, it is not metabolized to a GABA receptor agonist. In animal models, pregabalin binds to presynaptic voltage-gated calcium channels at the alpha-2-delta subunit in central nervous system tissues. Binding of the alpha-2-delta subunit decreases the depolarization-induced influx of calcium into neurons and reduces the release of excitatory neurotransmitters. This action may account for the anticonvulsant and analgesic effects of pregabalin. Pregabalin has no known activity at sodium channels, dopamine receptors, serotonin receptors, opiate receptors and does not modify cyclooxygenase activity.


Pregabalin is administered orally and is available in capsules or oral solution. Following oral administration, pregabalin reaches peak plasma concentrations within 1.5 hours and achieves steady state within 24 to 48 hours. The absorption of pregabalin is independent of the dose. Pregabalin readily crosses the blood-brain barrier. Humans cannot significantly metabolize pregabalin. Its elimination is primarily as an unchanged drug (less than 2% metabolized) by renal excretion. In patients with normal renal function, the mean elimination half-life is 6.3 hours. Researchers have studied pregabalin at dosages up to 600 mg/day. However, they did not find 600 mg/day to provide significant additional benefit and was less well tolerated due to side effects.

When discontinuing pregabalin, the recommendation is to taper the drug gradually over one week. In patients with seizure disorders, withdraw pregabalin gradually to minimize the risk of increased seizure.

  • Management of Neuropathic Pain Associated with Diabetic Peripheral Neuropathy: The recommended maximum therapeutic dose is 300 mg/day. The suggested starting dose is 50 mg three times per day. The dose can increase up to 300 mg/day within one week of starting treatment.
  • Management of Neuropathic Pain Associated with Spinal Cord Injury: The recommended therapeutic dose is 150 mg to 600 mg per day. The recommended starting dose is 75 mg twice per day. The dose may be increased to 150 mg twice per day within one week of initiating treatment. Patients with suboptimal pain relief following 2 to 3 weeks of treatment with 150 mg twice a day may be increased up to 300 mg twice per day. In spinal cord injury, pain improvement can be seen as early as one week after initiating treatment. However, to evaluate the efficacy of pregabalin, it is recommended to try the medication for 4 to 6 weeks, if tolerated by the patient.
  • Management of Postherpetic Neuralgia: The recommended therapeutic dose is 150 mg to 300 mg per day, divided into twice per day or three times per dosing. The recommended starting dose is 75 mg two times per day or 50 mg three times per day. The dose can increase up to 300 mg per day within one week of starting treatment. Patients with suboptimal pain relief after 2 to 4 weeks of treatment with 300 mg per day can be increased to 600 mg per day, divided into twice per day or three times per dosing.  
  • Management of Fibromyalgia: The recommended therapeutic dose is 300 mg to 450 mg per day. The recommended starting dose is 150 mg/day divided into twice per day dosing. The dose can increase to 300 mg per day within one week of starting treatment. Patients with suboptimal pain relief on 300 mg per day may be further increased to 450 mg per day, divided into twice per day dosing.
  • Adjunctive Therapy for Adults with Partial Onset Seizures: Pregabalin is FDA-approved only as an adjunctive for the treatment of partial-onset seizures. The effective dose is 150 mg to 600 mg per day, divided into twice per day or three times per dosing. The suggested starting dose is no greater than 150 mg per day. The total dose can increase to a maximum of 600 mg per day.  
  • Dosing Modifications: Pregabalin is eliminated primarily by renal excretion. Adjust the dose in patients with impaired renal function. Refer to prescription drug manufacturer information for further recommendations on dose reductions for patients with reduced creatinine clearance and those undergoing hemodialysis, according to the manufacturer. Although not explicitly studied, because pregabalin is not protein-bound, it is unlikely that patients with hepatic impairment require dosing modifications.

Adverse Effects

The majority of reported adverse effects caused by pregabalin were mild to moderate intensity, dose-dependent, and occurred within the first two weeks of initiating treatment. The most common adverse events were those affecting the central nervous system (CNS). Somnolence and dizziness occurred most frequently and were the most common adverse reactions that lead to discontinuation of pregabalin. The most common adverse reactions reported across all patient populations in premarketing controlled trials which occurred in greater than or equal to 5% of patients taking pregabalin and twice the rate reported by patients receiving placebo were: somnolence, dizziness, blurred vision, difficulty with concentration/attention, dry mouth, edema, and weight gain.[5][6][7]

Weight gain associated with pregabalin is dose-dependent and occurred in up to 14% of patients receiving 600 mg per day.

Following rapid or abrupt discontinuation of pregabalin, some patients reported symptoms including insomnia, nausea, headache, anxiety, nervousness, irritability, hyperhidrosis, and diarrhea.


Pregabalin is contraindicated in patients who have a known hypersensitivity to pregabalin. Hypersensitivity reactions have occurred in patients receiving pregabalin, including angioedema. There are no adequate studies with pregabalin in pregnant women. Pregabalin may cause fetal harm. Advise patients there is a potential risk to the fetus.

Pregabalin has been detected in the milk of lactating women; thus, breastfeeding is not a recommendation.


Antiepileptic drugs such as pregabalin may increase the risk of suicidal thoughts or behavior. Monitor patients under treatment with pregabalin for symptoms of new or worsening depression, suicidal ideation or behavior, and other changes in behavior or mood.


There is limited information regarding overdose with pregabalin. The highest known accidental overdose of pregabalin during clinical development was 8000 mg; this event was without significant clinical consequences. There is no specific antidote for overdose with pregabalin.

Enhancing Healthcare Team Outcomes

Pregabalin is a widely used medication for the management of seizures and pain disorders. While the drug is relatively safe, the primary care provider, pharmacist, nurse practitioner, and internist must regularly monitor the patient. The drug is known to cause depression and suicidal thoughts, so a mental assessment is advisable at each visit. Patients should be educated about the other side effects and told not to drive when taking the drug or combine it with other anti-seizure medications or alcohol. The patient should have a neurologist consult before making a change in the dose.[8] [Level 2]




[1] Abou-Khalil BW, Update on Antiepileptic Drugs 2019. Continuum (Minneapolis, Minn.). 2019 Apr;     [PubMed PMID: 30921021]
[2] Goodman CW,Brett AS, A Clinical Overview of Off-label Use of Gabapentinoid Drugs. JAMA internal medicine. 2019 Mar 25;     [PubMed PMID: 30907944]
[3] Parikh SK,Silberstein SD, Current Status of Antiepileptic Drugs as Preventive Migraine Therapy. Current treatment options in neurology. 2019 Mar 18;     [PubMed PMID: 30880369]
[4] Bendtsen L,Zakrzewska JM,Abbott J,Braschinsky M,Di Stefano G,Donnet A,Eide PK,Leal PRL,Maarbjerg S,May A,Nurmikko T,Obermann M,Jensen TS,Cruccu G, European Academy of Neurology guideline on trigeminal neuralgia. European journal of neurology. 2019 Mar 12;     [PubMed PMID: 30860637]
[5] Preuss CV,Kalava A,King KC, Prescription of Controlled Substances: Benefits and Risks 2019 Jan;     [PubMed PMID: 30726003]
[6] Derry S,Bell RF,Straube S,Wiffen PJ,Aldington D,Moore RA, Pregabalin for neuropathic pain in adults. The Cochrane database of systematic reviews. 2019 Jan 23;     [PubMed PMID: 30673120]
[7] Drugs for chronic insomnia. The Medical letter on drugs and therapeutics. 2018 Dec 17;     [PubMed PMID: 30625122]
[8] Bidari A,Moazen-Zadeh E,Ghavidel-Parsa B,Rahmani S,Hosseini S,Hassankhani A, Comparing duloxetine and pregabalin for treatment of pain and depression in women with fibromyalgia: an open-label randomized clinical trial. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences. 2019 Mar 14;     [PubMed PMID: 30877484]