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KING KHALID UNIVERSITY HOSPITAL

PHARMACY TEAM

MINUTES OF THE MEETING

Month: 29

th

September Location: Director of Pharmacy office

Date/Time : 29-09-2012 (13-11-1433H) 12.30pm to 2.30pm

Chairman of the Committee : Dr. Almajed Total # of Members : 8

Quorum Complete : 8

Present Members Dr. Ayed Al Shamrani Dr. Ahmed Hersi

Dr. Anwar Jammah Dr. Zainab Habib

Dr. Mohammad Moufleh Ph. Mohammad Blaihes

Dr. Randa Jaroudi Apologized members

ISSUE NO. TOPIC MATTERS ARISED

(Discussion / Conclusion / Recommendation)

RESPONSIBLE PERSON

TIME FRAME STATUS

Approval of Previous Minutes of the Meeting

Done Dr. Almajed

Unfinished Business

New Business

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Sertraline Hydrochloride (Lustral®)

Generic Name: Sertraline Hydrochloride Brand Name: Lustral®

Dosage form & Strength: 25-50mg oral Tablets

Requested by: Dr. Abdulqader Al-Jarad (Psychiatric Department) Requested Indication: Major depressive disorder, Anxiety disorder,

Labeled Indications: MDD, OCD, PD, PTSD, Social Anxiety disorder.

Approved organizations: USA, KSA, UK, Canada, Sweden Similar drugs available in KKUH formulary:

 Citalopram  Escitalopram  Fluoxetine  Fluvoxamine  Paroxetine  Fluoxetine

Conclusion of Efficacy & safety studies:

 Sertraline approved by FDA in 1996 for several indication.

 It is the shortest half life of the currently available SSRI in the markets and one of the most effective and safe antidepressant.

 One of the unique finding than other SSRI, the positive cardiac outcome in patients with HF. It is produced greater reductions in platelet/endothelial activation as compared with placebo and may offer further advantage for this patient population.

 In acute bipolar depression no significant difference between adjunctive bupropion, sertraline or venlafaxine was revealed among response or remission rates.

 Approved to be used in pediatric OCD. It has place in therapy for wide range of psychiatric illness.

 Advantages:

The shortest half life of the currently available SSRI and safest in breast feeding.

Cost:

 Cost/tablet: 3.6 SR

 Cost/pack: 30 tablet-108 SR PT Committee decision:

PT committee refused to add Sertraline Hydrochloride (Lustral® ) to

the KKUH Formulary due to there are more than 6 SSRI drugs available in the formulary with the same MOA and side effect, plus there isn’t any advantage of sertraline over the other to be add it. PT will discuss SSRI group with Dr Khalid bazaid in next meeting.

Dr. Solafa Fatani

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Paroxetine Hydrochloride (Seroxat CR®)

Generic Name: Paroxetine CR Brand Name: Seroxat CR®

Dosage form & Strength: 12.5mg, 25mg oral tablet

Requested by: Dr. Khalid Bazaid (Psychiatric department) Requested Indication: Approved Indications- Major depressive

disorder, Panic disorder, Social anxiety disorder, Premenstrual dysphoric disorder.

Approved organizations: ***

Similar drugs available in KKUH formulary:

 Paroxetine IR

 Citalopram

 Escitalopram

 Fluoxetine

 Fluvoxamine

Conclusion of Efficacy & safety studies:

 Paroxetine CR is a controlled-release formulation of the SSRI Paroxetine. It was introduced in 2002 as enteric film-coated tablet containing a degradable polymeric matrix using a technology called Geomatrix™. The enteric coat on Paroxetine CR delays the drug release until the tablet has left the stomach. This effect may avoid the stimulation of gastric 5-HT receptors, which is associated with gastrointestinal side effects, in

particular nausea.

 The polymeric matrix of paroxetine CR controls the dissolution rate; approximately 80% of the dose is absorbed over 4–5 h and the remaining 20% is retained in the tablet and does not enter the systemic circulation. Therefore, the equivalent dose of paroxetine CR needs to be 20–25% higher than that of Paroxetine (that to say 25 mg CR is equivalent to 20mg IR).

 The available tablet formulation of paroxetine CR is 12.5, 25 and 37.5 mg/day, while Paroxetine has 10, 20, 30 and 40 mg/day.

Advantage:

Paroxetine CR was effective as well as paroxetine IR in depression but was better tolerated and associated with low rates of early-onset nausea and dropout rates due to adverse events comparable to those of placebo

Cost:

 Cost/Pack : 12.5mg: 63 SR (30Tablet) 25mg: 84 SR (30Tablet) PT Committee decision:

PT Committeedecided not to be add Paroxetine CR to the KKUH

formulary. There is not much advantage over IR.

Dr. Solofa Fatani

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(Xarelto®) Brand Name: Xarelto®

Dosage form & Strength: 20mg oral tablet Requested by: F. Alhussain, A. Kareem Almomen

Requested Indication: Prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation, Treatment of deep vein thrombosis (DVT), and prevention of recurrent DVT and pulmonary embolism (PE) following an acute DVT in adults. Approved organizations: USA, UK, Canada

Similar drugs available in KKUH formulary:

 Enoxaparin

 Warfarin

Efficacy & safety studies:

 The annual rate of the primary safety outcome was not significantly different between the rivaroxaban and warfarin groups. Each of the annual rates of critical, fatal and

intracranial bleeding was significantly lower with rivaroxaban compared with warfarin.

 The primary outcome was confirmed in 2.1% of patients in the rivaroxaban group and 3.0% of patients in the enoxaparin/VKA group, favoring rivaroxaban, and demonstrating the non-inferiority versus combined parenteral enoxaparin/oral VKA regimen in the initial treatment of DVT and prevention of recurrent VTE.

 The incidence of treatment-emergent adverse events, excluding bleeding and recurrent VTE, was comparable between the rivaroxaban and placebo treatment groups and, overall, was lower than in the EINSTEIN-DVT study.

Cost:

 Cost/Pack:: 15mg,20mg = 12 SR

 Cost/month: 15mg,2omg + 335 SR

PT Committee decision:

PT Committee approved for new indication of rivaroxaban which are treatment of DVT, prevention of recurrent DVT, and to be restricted to hematology department only.

For prevent stroke indication, PT committee will send letter to cardiology for their opinion.

Al-Homaidah

Aprepitant/Fosaprepitant

(Emend/ IV Emend

®

)

Generic Name: Aprepitant/Fosaprepitant

Brand Name:

Emend/ IV Emend

®

Dosage form & Strength:

 Aprepitant -Oral Capsules: 40mg, 80mg, 125mg

 Fosaprepitant- IV, 115mg, 150mg

Requested by: Dr. Ahmed Al-Sagheir (Hematology/Oncology Department)

Dr. Haya Al-Salloum

(5)

Requested Indication:

 Chemotherapy induced nausea and vomiting, Due to highly emetogenic chemotherapy, including high-dose cisplatin, Prophylaxis

 Chemotherapy induced nausea and vomiting, Due to moderate emetogenic chemotherapy, Prophylaxis

 Post operative nausea and vomiting, Prophylaxis Approved organizations: USA, UK

Similar drugs available in KKUH formulary:

 Metoclopramide

 Granisteron

 Dexamethasone

Efficacy & safety studies:

 According to many evidences & studies, addition of aprepitant is more effective in controlling acute & delayed nausea & vomiting induced by highly & moderately chemotherapy than standard regimen including 5-HT3 antagonists & corticosteroids.

 Oral aprepitant is indicated in combination with other antiemetic agents for the prevention of nausea and vomiting associated with moderately- and highly-emetogenic cancer chemotherapy

 Aprepitant-containing anti-emetic regimen (in combination with dexamethasone and ondansetron) has been shown to be superior to the standard therapy

 Fosaprepitant dimeglumine is rapidly converted to aprepitant. Cost: 500 SR / 3days

 Cost-effectiveness of aprepitant regimen against standard regimen showed that, aprepitant regimen is more cost-effective than conventional regimens.

PT Committee decision: PT Committee agreed to be added

Fosaprepitant IV

(IV Emend

®) to the KKUH formulary.

Eltrombopag (Revolade®)

Generic Name: Eltrombopag Brand Name: Revolade ®

Dosage form & Strength: 25mg, 50mg oral tablets. Requested by: Dr. A. Almomen (Oncology/Hematology Department).

Requested Indication: Refractory ITP (FDA approved) Approved organizations: USA, UK, KAS, Canada

Similar drugs available in KKUH formulary: Romiplostim Efficacy & safety studies:

 There is no published study comparing efficacy and safety of Romiplastim and eltrombopag, but each drug showed comparable efficacy and safety in the literature.

Dr. Haya Al-Salloum

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 There is no head to head comparison between romiplostim and eltrombopag in the literature

 Eltrombopag should be used in patients with ITP only and are at risk of bleeding Cost:  Cost/Pack: 25mg = 5024 SR 50mg = 10049 SR  Cost/month: 25mg = 10049 SR 50mg = 15073 SR PT Committee decision:

PT Committee not agreed to add Eltrombopag (Revolade ®)to

KKUH Formulary, due to PT committee approved Romiplastin has

similar class few months ago and restricted to hematology. Non formulary Drugs

None Letter

Dr. Abdullah

Mobeirek letter:

Crestor

The letter shows the advantage of crestor and objected about PT C decision for refusing to add crestor to hospital formulary.

Crestor refused to be added to KKUH formulary few months ago by PT C and the policy for any drug rejected need one year to be reevaluate it again and discus it by PT C.

Dr. F. Al- Hussan

request for Crestor

crestor request for stroke prevention: clinical review by clinical pharmacist need for this indication.

Dr. Hersi letter:

Pulmonary

Hypertension

medication

Dr Hersi need to increase number of PHT patients on sildegril and cloprost up to 50 patients per year for cardiology patients

PT C decision: Need clinical review of PHT guideline and the best treatment.

Dr Hazem Al Mandel

letter:

Postin

Need to change dosage form of prostin vaginal sup. to propess form.

PTC decision: need to discuss and approve letter from gynecology department.

Next Meeting

Prepared by:

Noted by:

(7)

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