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Lamotrigine

Volume 330: debated on Monday 26 April 1999

The text on this page has been created from Hansard archive content, it may contain typographical errors.

To ask the Secretary of State for Health, pursuant to his answer of 30 March 1999, Official Report, columns 656-57, on Lamotrigine, if he will list for each of the 35 inquiries referred to (a) the incident or event which gave rise to the inquiry, (b) the name and address of the person who generated the inquiry, (c) details of the nature of the inquiry and (d) the steps which (i) his Department and (ii) the Medicines Control Agency have taken in response to the inquiry. [80231]

[holding answer 13 April 1999]: Details of the 35 inquiries received by the Medicines Control Agency relating to lamotrigine from health professionals and members of the public since the marketing authorisation was granted are shown in the table. In many cases, the incident or event which gave rise to the inquiry is not known. Under the Data Protection Act the names and addresses of the inquirers have been withheld and cannot be provided without the written permission of the individuals concerned. In most cases, the nature of the inquiries was to seek information on adverse drug reactions to lamotrigine, which is routinely provided on request to health professionals and members of the public by the Medicines Control Agency.

Inquiries relating to lamotrigine received by the Medicines Control Agency up to April 1999
Reason for inquiryInquirerNature of inquiry (information requested)Response
Not knownDoctorInformation on reduced white blood cell count with carbamazepine and lamotrigineDrug Analysis Prints1 (DAPs) provided
A patient with hair lossDoctorInformation on hair loss with lamotrigineDAP and details of reports of hair loss provided
An ADR reporting studyDoctorInformation on ADR reports in the Grampian Region for citalopram, gabapentin, lamotrigine, moclobemide, nefazodone, tramadol, venlafazine, topiramate and fentanyl patchesDetails of reports provided
Inquiries relating to lamotrigine received by the Medicines Control Agency up to April 1999
Reason for inquiryInquirerNature of inquiry (information requested)Response
A Pathologist had carried out an autopsy on patient who had taken lamotrigineDoctorInformation on deaths reported in association with lamotrigineDAP and details of fatal reports provided
Not KnownDoctorInformation on ADRs with lamotrigine (Particularly aggression)DAP provided
Not KnownPharmacistInformation ADRs to lamotrigine (Particularly liver reactions)DAP provided
The doctor was reporting a patient with dizziness and vomiting on lamotrigineDoctorInformation on ADRs to lamotrigineDAP provided
The inquirer was editing a textbookDoctorInformation related to psychiatric ADRs with gabapentin, lamotrigine, vigabatrin, topiramate, clobazam and felbamateDAP provided
Not KnownDoctorInformation on ADRs with lamotrigineDAP provided
Not KnownDoctorInformation on ADRs with lamotrigineDAP Provided
The inquirer was carrying our research on ADRs with antiepilepticsDoctorInformation on ADRs with lamotrigine, vigabatrin, gabapentinDAPs provided
The inquirer needed information for a court reportDoctorInformation on cases of aggression, agitation, confusion, personality change and restlessnessInformation on reports provided
Not KnownPharmacistInformation on ADRs with lamotrigineDAP provided
Not KnownDoctorInformation on yellow macular pigment with carbamazepine and lamotrigineDAPs provided
Not knownDoctorInformation on uveitis with lamotrigine and sodium valproateDAPs provided
Not knownPharmacistInformation on lamotrigine and carbamazepine and ecchymoses and capillary fragilityDAPs provided
Not KnownDoctor Information on ADRs with lamotrigineDAP provided
Inquiries relating to lamotrigine received by the Medicines Control Agency up to April 1999
Reason for inquiryInquirerNature of inquiry (information requested)Response
Not knownPharmacistInformation on lamotrigine and hormone replacement therapy when used togetherDAPs provided
Concern over press coverage of lamotrigine and skin reactionsDoctorFurther information requestedInformation provided over telephone
Not knownPharmacistInformation on pruritus and rashes with lamotrigineDAP provided
Not knownPharmacistInformation on gastrointestinal blockage vigabatrin, carbamazepine and lamotrigineDAPs provided
Two patients on sodium valproate developed thrombocytopenia when lamotrigine was addedPharmacistInformation on any other reports involving sodium valproate and lamotrigineDetails of relevant reports provided
Not knownPharmacistInformation on visual hallucinations with lamotrigineDAP and details of reports provided
Not knownDoctorInformation on hypogammaglobinaemia with lamotrigine and vigabatrinDAPs provided
Not knownPharmacistInformation on urinary incontinence with lamotrigineDAPs provided
Not knownPharmacistInformation on ADRs with lamotrigineDAP provided
Not knownDoctorInformation on ADRs with gabapentin, vigabatrin and lamotrigineDAPs provided
Not knownPharmacistInformation on raised liver enzymes with lamotrigineDAP provided
Not knownPharmacistInformation on ADRs with lamotrigine and haloperidolDAPs provided
Not knownPharmacistInformation on ADRs indomethacin and diclofenacDAPs provided
Not knownDoctorInformation on psychiatric ADRs with lamotrigineDAP provided
Issue of skin reactionsRegulatory authorityInformation on serious skin reactions with amotrigineDetails of reports provided
Inquiries relating to lamotrigine received by the Medicines Control Agency up to April 1999
Reason for inquiryInquirerNature of inquiry (information requested)Response
Not knownMember of the publicInformation on ADRs with lamotrigineDAP provided
Confusion over the brand names Lamicta and LamasilGP Practice ManagerInquiry as to whether there was a list of drugs with similar names which could cause confusion No such list was known
Parliamentary questionMartin Redmond MPWhat research his Department has carried out into a comparison of lamotrigine and valproate monotherapy in patients with primary generalised seizures; with what findingsHansard reference 263 c922-3W
1A Drug Analysis Print (DAP) gives a complete list of all suspected adverse reactions reported through the Yellow Card Scheme to the Committee on Safety of Medicines (CSM)/Medicines Control Agency (MCA) in association with the named drug substance.