Page 8 - Pharma GIT L1
P. 8

4. 5HT3 antagonists:                                    They block 5HT3                                                                                             Headache.



                              Ondansetron.                                  receptors in CTZ.                                                                                         GIT upsets.



                              Granisetron.



                              Dolasetron.



                    All are equivalent in efficacy, adverse effects, convenience & cost.


                    Very effective in controlling acute nausea & vomiting associated with ordinary dose chemotherapy.



                    Less effective in controlling delayed emesis & that due to high dose cancer chemotherapy.



                    Used in Vomiting caused by cytotoxic drugs (Ondansetron is the drug of first choice).


                  5. Neurokinin (NK1)                                                                                              Used for prevention



                       receptor blocker:                                                                                              of acute & delayed



                              Aprepitant.                                                                                            vomiting associated


                                                                                           ----                                       with highly                                                      ---



                                                                                                                                      emetogenic cancer



                                                                                                                                      chemotherapy.


                  6. Tetrahydrocannabinol:                                Marijuana derivative.                                                                                       General CNS



                              Nabilone.                                  Cannabinoid receptors                                                                                          disturbances.



                                                                             agonist.                                                                                                  Anti-parasympathetic


                                                                                                                                                                                          effects.



                                                                                                                                                                                       Drowsiness.
   3   4   5   6   7   8   9   10   11