SECTION 1:
Tegretol Tablets 100mg and Tegretol Tablets 400mg changed to Tegretol 100mg Tablets and Tegretol 400mg Tablets respectively
SECTION 2:
Tablets and Chewtabs - 5 Carbomyl 5-11 dibenz(b,f)azepine changed to: 5H-dibenzo[b,f]azepine-5-carboxamide
SECTION 4.3:
The following has been added:
hepatic porphyrias (e.g......variegate porphyria, porphyria cutanea tarda).
The following has been deleted from the 3rd paragraph:
Because it is structurally related to tricyclic anti-depressants
SECTION 4.4
Paragraph on hypersensitivity reworded:
Tegretol may trigger hypersensitivity reactions, including multi-organ hypersensitivity reactions, which can affect the skin, liver, haematopoietic organs and lymphatic system or other organs, either individually or together in the context of a systemic reaction (see section 4.8 Undesirable effects).
In general, if signs and symptoms suggestive of hypersensitivity reactions occur, Tegretol should be withdrawn immediately.
Patients who have exhibited hypersensitivity reactions to carbamazepine should be informed that 25-30 % of these patients may experience hypersensitivity reactions with oxacarbazepine (Trileptal).
Paragraph on Tegretol and oestrogen and/or progestogen preparations: The following paragraph has been deleted:
There have been a few cases of neonatal seizures and/or respiratory depression associated with maternal Tegretol and other concomitant anti-epileptic drug use. A few cases of neonatal vomiting, diarrhoea and/or decreased feeding have also been reported in association with maternal Tegretol use. These reactions may represent a neonatal withdrawal syndrome.
SECTION 4.5
The following paragraph has been added:
Carbamazepine is a potent inducer of CYP3A4 and other phase I and phase II enzyme systems in the liver, and may therefore reduce plasma concentrations of comedications mainly metabolized by CYP3A4 by induction of their metabolism.
Agents that may raise plasma levels:
The following have been added - omeprozole, trazodone, vigabratim, voriconazole, olanzepine, quetiapine.
The following have been deleted - ibuprofen, viloxazine, nefazodone, stiripentol, oxybutynin, dantrolene, triclopidine, loxapine, valpromide.
Agents that may decrease levels:
The following have been added – fosphenytoin, aminophylline
Sentence reading “On the other hand, valproic acid and primidone have been reported to raise the plasma levels….” has been deleted
Effect of Tegretol on plasma levels of concomitant agents:
The following have been added – paracetamol, acenocoumarol, bupropion, citalopram, trazodone, quetiapine, imatinib.
The following have been deleted – everolimus, bromperidol, phenazone (antipyrine).
The paragraph on MIOAs has been deleted.
Combinations to be taken into consideration:
Paragraph on paracetamol deleted.
SECTION 4.6
The following paragraphs have been added:
During pregnancy, an effective antiepileptic treatment must not be interrupted, since the aggravation of the illness is detrimental to both the mother and the fetus.
There have been a few cases of neonatal seizures and/or respiratory depression associated with maternal Tegretol and other concomitant antiepileptic drug use. A few cases of neonatal vomiting, diarrhoea and/or decreased feeding have also been reported in association with maternal Tegretol use. These reactions may represent a neonatal withdrawal syndrome.
SECTION 4.8
Frequencies given as figures rather than percentages.
The following have been added: pancytopenia, variegate porphyria, porphyria cutanea tarda, blood osmolarity decreased, osteoporosisneuropathy, increased intraocular pressure, pulmonary embolism, dermatitis, spermatogenesis abnormal (with decreased sperm count and/or motality).
SECTION 5.1
ATC code changed from N03 AX to No3 AF01
SECTION 5.2:
The following has been deleted:
Carbamazepine is metabolised in the liver, where the epoxide pathway of biotransformation is the most important one, yielding the 10, 11-transdiol derivative and its glucuronide as the main metabolites.
Cytochrome P450 3A4 has been identified as the major isoform responsible for the formation of carbamazepine 10, 11-epoxide from carbamazepine. 9-Hydroxy-methyl-10-carbamoyl acridan is a minor metabolite related to this pathway. After a single oral dose of carbamazepine about 30% appears in the urine as end-products of the epoxide pathway.
Other important biotransformation pathways for carbamazepine lead to various monohydroxylated compounds, as well as to the N-glucuronide of carbamazepine