Lyrica blue and white capsule

If you are a consumer or patient please visit this version. However, due to Pfizer's marketing exclusivity rights, this drug product is not labeled with that pediatric information. Pregabalin capsule is given orally with or without food.

If you are a consumer or patient please visit this version. DPN Pain 2. Fibromyalgia 2. Dose should be adjusted in patients with reduced renal function. Administer the total daily dose in two or three divided doses. In view of dose-dependent adverse reactions and since LYRICA is eliminated primarily by renal excretion, adjust the dose in patients with reduced renal function. Base the dose adjustment in patients with renal impairment on creatinine clearance CLcr , as indicated in Table 1.

Lyrica blue and white capsule

Pregabalin belongs to the class of medication known as analgesics. It is used to relieve neuropathic pain associated with diabetic peripheral neuropathy pain from damaged nerves due to diabetes and postherpetic neuralgia persisting pain following healing of the rash due to shingles. Pregabalin is also used to relieve pain associated with fibromyalgia pain in the muscles, ligaments, and tendons. It is also useful in managing central neuropathic pain pain from damaged nerves of the brain and spinal cord. Pain from damaged nerves may feel sharp, burning, tingling, shooting, or numb. It is not known exactly how pregabalin works, but it is thought to work in the brain to decrease the release of chemicals responsible for pain. For some people, improvement in pain may occur as early as the first week of treatment with pregabalin. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms of this medication may not be used for all of the conditions discussed here. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor.

However, in cultured neurons prolonged application of pregabalin increases the density of GABA transporter protein and increases the rate of functional GABA transport. Adjunctive Therapy for Partial-Onset Seizures in Adult Patients The efficacy of pregabalin as adjunctive lyrica blue and white capsule for partial-onset seizures in adult patients was established in three week, randomized, double-blind, placebo-controlled, multicenter studies. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed.

.

If you are a consumer or patient please visit this version. Because LYRICA is eliminated primarily by renal excretion, adjust the dose in adult patients with reduced renal function [see Dosage and Administration 2. The recommended dosages for adults and pediatric patients 1 month of age and older are included in Table 1. Administer the total daily dosage orally in two or three divided doses as indicated in Table 1. In pediatric patients, the recommended dosing regimen is dependent upon body weight. Based on clinical response and tolerability, dosage may be increased, approximately weekly. Patients who do not experience sufficient pain relief after 2 to 3 weeks of treatment with mg two times a day and who tolerate LYRICA may be treated with up to mg two times a day [see Clinical Studies In view of dose-dependent adverse reactions and since LYRICA is eliminated primarily by renal excretion, adjust the dose in adult patients with reduced renal function.

Lyrica blue and white capsule

Lyrica is a brand-name prescription medication. Lyrica is also FDA-approved to treat partial onset seizures in children ages 1 month and older. For this purpose, Lyrica is used with other seizure drugs. Lyrica belongs to a drug class called antiepileptic drugs. A drug class is a group of medications that work in a similar way. Lyrica comes as capsules that you swallow. Lyrica capsules are available in the following strengths:. Yes, Lyrica is a controlled substance.

Opinionated meaning in hindi

NDC National Drug Code - Each drug product is assigned this unique number which can be found on the drug's outer packaging. Advise patients that LYRICA may cause angioedema, with swelling of the face, mouth lip, gum, tongue and neck larynx and pharynx that can lead to life-threatening respiratory compromise. Mean renal clearance was estimated to be Population pharmacokinetic analyses in patients treated with pregabalin and various concomitant medications suggest the following:. The fraction of patients achieving various levels of improvement in pain intensity from baseline to Week 12 is presented in Figure A no-effect dose was not established. In view of dose-dependent adverse reactions and since LYRICA is eliminated primarily by renal excretion, adjust the dose in patients with reduced renal function. It is inactive at serotonin and dopamine receptors and does not inhibit dopamine, serotonin, or noradrenaline reuptake. Clinical experience during LYRICA's premarketing development provides no direct means to assess its potential for inducing tumors in humans. How should I store pregabalin capsules? Do not engage in activities requiring mental alertness, such as driving or operating machinery, until you know how this medication affects you. If you are a consumer or patient please visit this version. Do not start a new medicine without talking with your healthcare provider.

Pregabalin is a prescription drug. It comes in three forms: a capsule, a solution, and an extended-release tablet. All forms are taken by mouth.

Inform patients that if changes in vision occur, they should notify their physician [see Warnings and Precautions 5. Available clinical study data in patients greater than 12 years of age do not provide a clear conclusion about the potential risk of tumorigenicity with pregabalin [ see Warnings and Precautions 5. Before taking pregabalin capsules, tell your healthcare provider about all your medical conditions, including if you: have or have had depression, mood problems or suicidal thoughts or behavior. Gabapentin pharmacokinetics following single- and multiple-dose administration were unaltered by pregabalin coadministration. In preclinical studies in rats, pregabalin was associated with an increased risk of male-mediated teratogenicity. Nonmedicinal ingredients: ammonium hydroxide, gelatin, iron oxide black, pregelatinized starch, propylene glycol, shellac glaze, talc, red iron oxide, and titanium dioxide. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Mutagenesis Pregabalin was not mutagenic in bacteria or in mammalian cells in vitro , was not clastogenic in mammalian systems in vitro and in vivo , and did not induce unscheduled DNA synthesis in mouse or rat hepatocytes. Pregabalin treatment may cause peripheral edema. When the decision is made to co-prescribe pregabalin with another CNS depressant, particularly an opioid, or to prescribe pregabalin to patients with underlying respiratory impairment, monitor patients for symptoms of respiratory depression and sedation, and consider initiating pregabalin at a low dose.