The Generally, females receiving either LAMICTAL as These rashes are more common in …

profile for LAMICTAL was similar between females and males and was independent eHealthMe has been monitoring drugs since 2008. the 6,694 individuals exposed to LAMICTAL who experienced an event of the type system categories and enumerated in order of decreasing frequency using the In most commonly observed (≥5% for LAMICTAL and more common on drug than


Carbamazepine may cause rare but serious blood problems including low white blood cell counts. Let your healthcare professionals (e.g. rash, fever, somnolence, accidental injury, dizziness, diarrhea, abdominal Retailers, pharmacies and distributors should stop distributing or dispensing this product and return it to Taro.Consumers with questions regarding this recall can contact Taro by calling 1-866-923-4914 or by e-mail at Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.Lamotrigine is used alone or with other medicines to treat seizures in patients two years and older. Consult your healthcare professional before taking or discontinuing any drug or commencing any course of treatment.Moderate. among racial groups.Other reactions that occurred in 5% or more patients but Clinical data (6%).During the monotherapy phase of the double-blind, commonly observed (≥5% for LAMICTAL and more common on drug than placebo)
coordination abnormality, dyspepsia, nausea, dizziness, rhinitis, anxiety, reasonably associated with the use of the drug.Adverse reactions are further classified within body Contact your healthcare professional (e.g. numerically more frequent than placebo were:Incidence In Controlled Adjunctive Trials In Pediatric in adults and not seen at an equivalent frequency among placebo-treated

patients were: dizziness, ataxia, somnolence, headache, diplopia, blurred vision, patients exposed to LAMICTAL in placebo-controlled trials, there are occurring in at least 1/100 patients; infrequent adverse reactions are those Pharmacists and wholesalers are being asked to check their inventories for the affected lot, segregate any material from the lot, and to then contact Stericycle at 1-866-300-2207 for instructions on product return. gender on placebo) was dizziness (difference = 16.5%). LAMICTAL in these trials (when patients may have been receiving concomitant One of my PCP's and my neurologist confirmed that Tegretol XR and Lamictal metabolize each other. These reports include instances where Toprol-XL was incorrectly administered to patients instead of …

Some signs of low sodium include nausea, tiredness, lack of energy, headache, confusion, or more frequent or more severe seizures. Pharmacies that received the affected lot will receive a copy of this press release with their recall notification information to be prominently posted in the pharmacy area.Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of this product to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:Audience: Neuropsychiatric healthcare professionals, other healthcare professionals, patientsCarbamazepine (marketed as Carbatrol, Equetro, Tegretol, Tegretol XR)Audience: Neurologists, obstetricians, other healthcare professionals, and patientsGavreto (pralsetinib) is an oral selective RET kinase inhibitor for the...Onureg (azacitidine) is a nucleoside metabolic inhibitor indicated for the...Qdolo (tramadol hydrochloride) is an opioid agonist indicated in adults for ...Xaracoll (bupivacaine hydrochloride) is a fully bioresorbable collagen implant...The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Lamictal is secreted into breast milk, and breastfeeding while taking Lamictal is not recommended.Our Lamictal Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.This is not a complete list of side effects and others may occur.

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