PharmaCare Newsletter
00-007
June 7, 2000
Compounded Prescriptions Update
This information is to clarify the eligibility of compounded prescriptions for PharmaCare coverage.
PharmaCare recognizes compounded prescriptions as rational combinations of active ingredients requiring professional judgement and technical skill in their preparation. The practice of including prescription items with non-prescription items, in an attempt to secure reimbursement, is inappropriate practice.
The following examples of compounds would NOT be eligible for coverage:
1. Preparations containing hydrocortisone or betamethasone compounded with non-benefit or over-the-counter products such as Nix® (permethrin) or Eurax® (crotamiton) cream, or an over-the-counter medicated base
2. Clindamycin in Reversa®, or any other OTC medicated base (exception-clindamycin in Duonalc® is eligible for coverage)
3. Topical NSAIDs
4. Topical hormone products - these include progesterone creams, testosterone cream, triple estrogen cream
5. Compounded estrogen capsules for oral use
At the present time, there are no randomized controlled trials to support the clinical use of topical NSAIDs and hormones and therefore such compounds are not eligible for PharmaCare coverage.
Note: All compounded preparations containing retinoic acid would only be a benefit if the physician had obtained a Special Authority for coverage of retinoic acid for the patient.
Compounds not eligible for coverage:
- Please use the non-benefit PIN # 66123252
- 921297 - Compounded Mixture
- 842435 - Compounded Ointment/Cream
- 842443 - Compounded Lotion
Should you have any questions concerning the eligibility of compounded prescriptions, please contact the PharmaNet Help Desk for clarification.
Please note that claims for non-benefit compounds which are submitted using any of the compound benefit PINs, will be subject to recovery upon audit.
Methadone - Reminder
Please ensure all claims for methadone maintenance are submitted as Methadone 1mg/ml, using PIN #999792, with no fee for Plans A and C.
When dispensing methadone prescriptions for pain management, submit claims under narcotic compounds, PIN #999776, and follow the normal billing practice for drug cost and fee.
PharmaCare will monitor the use of both PINs. Any methadone claims that are submitted using an inappropriate PIN will be subject to recovery.
Ipratropium 21 mcg Aerosol Nasal Spray
The following LCA items should be entered by number of doses, ie. 345, and NOT by ml.
- Alti-Ipratropium 21 mcg Nasal Spray DIN 2240072
- PMS-Ipratropium 21 mcg Nasal Spray DIN 2239627
- Atrovent® 21 mcg Nasal Spray DIN 2240072
Correction : Newsletter 00-01
Page #3, New Products Categorized to LCA and/or RDP:
DIN 2240682 should read " PMS- Fluvoxamine (fluvoxamine maleate) tabs 50 mg ", not
"PMS-Fluoxetine HCl 50mg"
LCA Update
Status Change: MORPHINE SR 30 mg and 60 mg ( M.O.S.® SR Tablets ICN )
Based on the recent price reduction, please be advised that effective August 1, 2000, M.O.S. SR tablets 30mg and 60mg will also be designated as full benefits.
PRODUCT and DIN
|
BENEFIT STATUS
|
M.O.S.® SR 30 mg Tablets din 776181
|
F
|
M.O.S.® SR 60 mg Tablets din 776203
|
F
|
BENEFITS
The following new drugs have been included
as eligible PharmaCare benefits on Plans A, B, C, E and F (criteria follows)
DIN
|
MAN
|
DRUG NAME
|
Short Term
|
Long Term
|
Plan G Eligible
|
2240334
|
KNR
|
Alti-Tryptophan (tryptophan) caps 500mg
|
|
Y
|
Y
|
2241887
|
TAR
|
Taro-Desoximetasone (desoximetasone) gel 0.05%
|
|
Y
|
|
2240295
|
LIL
|
Humalog® Mix25 (Pen)
|
|
Y
|
|
2241283
|
LIL
|
Humalog® Pen
|
|
Y
|
|
2239713
|
RXP
|
Rhoxal-Valproic (valproic acid) caps 500mg EC
|
|
Y
|
Y
|
2239714
|
RXP
|
Rhoxal-Valproic (valproic acid) caps 250mg
|
|
Y
|
Y
|
Humalog® Pens
Effective immediately, PharmaCare will provide partial coverage for Humalog® Pen and Humalog® Mix 25 Pen. Coverage for these products will be provided up to the average PharmaCare claimed price of human biosynthetic regular (short-acting) insulin, subject to the usual plan eligibility requirements and deductibles. Patients will be required to pay the difference in cost between the current PharmaCare maximum price (currently $1.9625 per ml) and the claimed price for Humalog® Pen and Humalog Mix 25® Pen.
NEW PRODUCTS CATEGORIZED TO LCA and/or RDP
The following new products will be included as benefits
under the LCA/RDP Program for Benefit Groups A, B, C, E, & F
DIN
|
MAN
|
DRUG NAME
|
FULL/
PARTIAL
|
LCA/RDP Price
|
Short Term
|
Long Term
|
Plan G Eligible
|
2241704
|
NOP
|
Novo-Gemfibrozil (gemfibrozil) caps 300mg
|
P
|
0.3545
|
|
Y
|
|
2241575
|
APX
|
APO-Levobunolol (levobunolol HCl) sol 0.25%
|
P
|
1.2399
|
|
Y
|
|
2241574
|
APX
|
APO-Levobunolol (levobunolol HCl) sol 0.5%
|
P
|
1.6113
|
|
Y
|
|
2241224
|
SIL
|
Sab-Diclofenac (diclofenac sodium) supp 50mg
|
P
|
0.6800
|
|
Y
|
|
2241225
|
SIL
|
Sab-Diclofenac (diclofenac sodium) supp 100mg
|
P
|
0.9408
|
|
Y
|
|
|
|
|
LCA and/or RDP (cont'd)
|
|
|
|
|
|
DIN
|
MAN
|
DRUG NAME
|
FULL/
PARTIAL
|
LCA/RDP Price
|
Short Term
|
Long Term
|
Plan G Eligible
|
2231327
|
NOP
|
Novo-Naprox SR (naproxen) tab SR 24h 750mg
|
P
|
0.8763
|
|
Y
|
|
2241826
|
YMG
|
Schein Amoxicillin (amoxicillin trihydrate) caps 250mg
|
P
|
0.1065
|
Y
|
|
|
2241827
|
YMG
|
Schein Amoxicillin (amoxicillin trihydrate) caps 500mg
|
P
|
0.2072
|
Y
|
|
|
2242177
|
YMG
|
Scheinpharm Fluoxetine caps 10mg
|
P
|
1.1502
|
|
Y
|
Y
|
2242178
|
YMG
|
Scheinpharm Fluoxetine caps 20mg
|
P
|
1.0718
|
|
Y
|
Y
|
DIN
|
MAN
|
DRUG NAME
|
Short Term
|
Long Term
|
2241007
|
FRS
|
Hyzaar® DS (losartan potassium/hctz) tabs 100-25mg
|
|
Y
|
2241818
|
SFY
|
Avalide® (irbesartan/hydrochlorothiazide) tabs 150/12.5mg
|
|
Y
|
2241819
|
SFY
|
Avalide® (irbesartan/hydrochlorothiazide) tabs 300/12.5mg
|
|
Y
|
2240867
|
NOP
|
Novo-Nabumetone (nabumetone) tabs 500mg
|
|
Y
|
- for the treatment of hypertension for patients who have experienced a cough with ACE inhibitors and who also require a diuretic.
Advair® (salmeterol+fluticasone), revised criteria
Coverage for Advair® (salmeterol+fluticasone) is currently available as a restricted benefit for the treatment of asthma for patients who require both corticosteroid and long-acting beta agonist therapy and have been previously stabilized on the above products for a period of time. Patients are required to have met the initial criteria for coverage of salmeterol.
Coverage for salmeterol is currently provided for patients experiencing breakthrough symptoms when given optimal corticosteroid and short-acting beta agonist therapy.
Based on the recommendations of PharmaCare's Drug Benefit Committee (DBC), the following changes will be in effect as of June 1, 2000:
1. Respirologists and allergists will be exempt from the special authority process, similar to the exemption for salmeterol. Written or verbal requests from these specialists groups will no longer be required for coverage of Advair®
2. PharmaCare will accept requests for Advair® coverage from pharmacists for patients who already have a current special authority approval for salmeterol and who are also receiving concomitant corticosteroid therapy.
NON-BENEFITS
PharmaCare's Drug Benefit Committee (DBC) recently completed the review of the following
products and recommended that these products not be added as a benefit
under the program (criteria follows)
DIN
|
MAN
|
DRUG NAME
|
2218488
|
UNK
|
Merrem® PWS IV (meropenem) vial 500mg
|
2218496
|
UNK
|
Merrem® PWS IV (meropenem) vial 1g
|
2219018
|
UNK
|
Merrem® add-vantage (meropenem) vial 500mg
|
2219026
|
UNK
|
Merrem® add-vantage (meropenem) vial 1g
|
2240863
|
GOW
|
Relenza® (zanamivir) 5mg
|
- currently intravenous therapy administered at home falls under the jurisdiction of the regional health boards and not under the mandate of PharmaCare.
- PharmaCare's Drug Benefit Committee (DBC) has completed the review of zanamivir and concluded that there is insufficient evidence from published randomized controlled trials to assess whether zanamivir provides a therapeutic advantage over placebo in the treatment of influenza.
- there is no evidence that zanamivir prevents any of the complications of influenza, ongoing morbidity as a result of an influenza episode, or mortality. The DBC noted concerns about the very low number of high-risk patients who participated in the studies and about the induction of bronchospasm in patients with asthma or other respiratory disease.
Cipro® IV Solutions: Change in benefit status
Currently intravenous therapy adminstered at home falls under the mandate of the Regional Health Boards and not under the mandate of the PharmaCare Program. Effective June 1, 2000, Cipro® IV solutions (DIN 2155982) will no longer be available as a benefit under this Program.
DRUGS UNDER REVIEW
The following drug submissions are currently under review by the Therapeutics Initiative, Pharmacoeconomics Initiative and the Drug Benefit Committee of PharmaCare.
ancestim (STEMGEN®)
alendronate (FOSAMAX®), resubmission
azithromycin (ZITHROMAX®), resubmission
bisoprolol (MONOCOR®)
celecoxib (CELEBREX®), resubmission
diazepam rectal gel (DIASTAT®)
epoprostenol (FLOLAN®), new indication
erythropoeitin (EPREX®), resubmission
filgrastim (NEUPOGEN®), new indication
fosfomycin tromethamine (MONUROL®)
imiquimod cream 5% (ALDARA®)
interferon alfacon-1 (INFERGEN®)
leflunomide (ARAVA®)
levonorgestrel (Plan B)
modafinil (ALERTEC®)
quetiapine (SEROQUEL®), resubmission
raloxifene HCl (EVISTA®), resubmission
risedronate sodium (ACTONEL®)
rizatriptan benzoate (MAXALT®)
rofecoxib (VIOXX®)
ropinirole HCl (REQUIP®), resubmission
rosiglitazone (AVANDIA®)
salmon-calcitonin 2000IU (MIACALCIN®)
tamsulosin (FLOMAX®), resubmission
zafirlukast (ACCOLATE®), resubmission
tizanadine (ZANAFLEX®)
|