| GENERIC NAME |
|
| Lansoprazole |
Pantoprazole will be automatically substituted for other proton
pump inhibitors. When administering PPIs via feeding tubes auto substitute
Lansoprazole Solutabs.
·
Pantoprazole (Protonix), injection and oral,
is the proton pump inhibitor of choice, with automatic substitution for
omeprazole (Prilosecâ), rabeprazole (Aciphexâ),
Lansoprazole (Prevacidâ), and other
oral proton pump inhibitors unless the physician has checked the dispense as
written block.
|
Dosing
Equivalence (mg) |
Lansoprazole
(Prevacid) |
Esomeprazole
(Nexium) |
Omeprazole
(Prilosec) |
Rabeprazole
(Aciphex) |
Pantoprazole
(Protonix) |
|
30 qd |
20 qd |
20 qd |
20 qd |
20 qd |
|
30 qd |
40 qd |
40 qd |
20 qd |
40 qd |
|
30 bid |
20-40 bid |
20-40 bid |
20 bid |
40 bid |
Lanoprazole Solutabs, 15 mg or 30 mg, may be mixed with water
and placed down a very small bore pediatric feeding tube. The granules do not
clump or adhere to the tube.
|
Lanoprazole |
Omeprazole |
|
1-11 years |
<= 30 kg |
15 mg qd |
>= 2 years |
< 20 kg |
10 mg qd |
|
|
> 30 kg |
30 mg qd |
|
>=20 kg |
20 mg qd |
|
12-17 years |
Non erosive GERD |
15 mg qd |
|
|
|
|
|
Erosive GERD |
30 mg qd |
|
|
|
Pantoprazole IV Criteria for use
·
Criteria for use of IV Proton Pump
Inhibitors (PPIs) are list below. If a patient does not meet criteria the
pharmacist will call the physician and/or leave a chart note recommending
conversion to oral therapy.
- Initial treatment of
patients with active upper GI tract bleeding, until they can tolerate oral
therapy, usually after three days of therapy.
- Initial treatment of
patients with Zollinger-Ellison syndrome, until they can tolerate oral therapy
- Stress-ulcer prophylaxis
for critical care patients
- Patients who require PPI
therapy who can not tolerate oral or NG PPI therapy
·
Patients on IV proton pump
inhibitors will have an order entered for the oral route allowing the nurse to
use the oral route when the patient is tolerating oral therapy. Proton pump
inhibitors may be given by the oral route if the patient
does not have active gastrointestinal
bleeding, malabsorption syndrome, short bowel syndrome, severe diarrhea,
uncontrolled nausea and vomiting, continuous nasogastric suctioning, and is not
at risk for aspiration.
|
| Leuprolide |
Leuprolide P&T Review
·
Depot Lupron is recommended for outpatient use, as its action is
time dependent and is indicated for treatment of chronic conditions that may be
treated on an outpatient basis. Depot Lupron provides serum levels that plateau
within two days after dosing and remain relatively stable for 4-5 weeks.
Injection of Depot Lupron initially stimulates pituitary gonadotropins followed
by prolonged suppression. Repeated dosing at monthly intervals results in
decreased secretion of gonadal steroids; consequently, tissues and functions
that depend on gonadal steroids for their maintenance become quiescent. The
biological effect is strictly time-dependent and not concentration-dependent.
·
Pharmacy will not routinely stock Depot Lupron.
·
Pharmacy will order and provide Lupron Depot 7.5 mg for
patients who are hospitalized and who are not anticipated to be discharged
within the next 5 days. Pharmacists will determine if the patient is nearing
discharge before dispensing Lupron.
·
Lupron will only be dispensed for FDA approved indications.
Pharmacists will verify the indication before dispensing Lupron.
|
| Levalbuterol |
Autosubstitution with
Albuterol
Levalbuterol is non-formulary. Albuterol has been previously approved for
automatic substitution at an equivalent dose for levalbuterol (two times
levalbuterol dose at the same frequency).
·
All
patients receiving levalbuterol (those who have orders stating dispense as
written) will be converted to an equivalent dose of
albuterol after 48 hours of therapy, unless they are allergic to albuterol,
receiving levalbuterol at home, or have acute atrial fibrillation. Objective
parameters will be monitored by respiratory therapy (heart rate, tremors,
nervousness, and blood gases if ordered)
from start of
levalbuterol to 48 hours after albuterol is started.
If a clinically significant decline is not seen, albuterol will be continued.
DUE Montoring form
·
Data will be collected on all patients, during levalbuterol
administration and after conversion to albuterol. This information will be
presented to the committee for their review. (see accompanying monitoring tool).
·
Currently Levalbuterol accounts for 19% of doses, but 87% of
$125,628 in total cost
|
| Levetiracetam |
-
Levetiracetam injection
is formulary restricted to the following patients:
-
Patients unable to take
oral levetiracetam
-
Oral bioavailability
is 100% and is unaffected by food or enteral nutritional products
-
Equivalent IV and
oral doses result in equivalent Cmax, Cmin, and total systemic exposure
-
levetiracetam
injection cost approximately 13 times more than the oral tablets
-
Status epilepticus
after benzodiazepines (lorazepam) and fosphenytoin have failed
-
No randomized
control trials have been completed for this indication. Only case reports are
available.
-
Levetiracetam oral
tablets cost $2.27 per 500 mg versus $29.15 per 500 mg injection ($58.30 for
1000 mg, and $175 for 3000 mg injection). Fosphenytoin injection cost $120.76
per 1000 mg
-
Pharmacist will
contact ordering physicians to convert to oral therapy when the patient is
able to take oral medications or has a functional feeding tube.
|
| Levofloxacin |
|
Dosage
Recommendations Per Package Insert |
|
|
Ciprofloxacin Ordered |
Levofloxacin Autosubstitution |
Moxifloxican Ordered |
|
Acute Bacterial Exacerbation of Chronic Bronchitis |
400 mg Q12H |
500mg Q24H x 7 days |
400 mg Q24H |
|
Acute Bacterial Sinusitis |
400 mg Q12H |
750mg Q24H 5 days |
400 mg Q24H |
|
Bone & Joint |
400 mg Q8-12H |
DO NOT SUBSTITUTE
|
|
|
Community Acquired Pneumonia |
|
750mg Q24H x 5 days |
400 mg Q24H |
|
Nosocomial Pneumonia |
400 mg Q8H |
750 mg Q24H x 7-14 days |
NOT INDICATED |
|
intra-abdominal |
400 mg q12H (plus metronidazole) |
750 mg Q24H (plus metronidazole) |
400 mg Q24H |
|
Uncomplicated UTI |
200 mg Q12H |
250mg Q24H x 3 days |
NOT INDICATED |
|
Complicated UTI |
400 mg Q12H |
250mg Q24H x 10 days |
NOT INDICATED |
|
Acute Pyelonephritis |
|
250mg Q24H x 10 days |
NOT INDICATED |
|
Chronic Bacterial Prostatitis |
400 mg Q12H |
500 mg Q24H x 28 days |
NOT INDICATED |
|
Uncomplicated Skin & Skin Structure Infection |
400 mg Q12H |
500 mg Q24H 7-10 days |
400 mg Q24H |
|
Complicated Skin and Skin Structure Infection |
400 mg Q8H |
750 mg Q24H 7-14 days |
400 mg Q24H |
|
Levofloxacin Package Insert Renal Dosing Guidelines |
|
Creatinine Clearance |
Nosocomial Pneumonia,
Community Acquired Pneumonia,
Complicated Skin & Skin Structure Infections,
Acute Bacterial Sinusitis |
ABECP,
Prostatitis,
Uncomplicated Skin and Skin Structure
Infection |
Complicate UTI,
Pyelonephritis |
|
>= 50 |
750 mg Q24H |
500 mg Q24h |
250 mg Q24H |
|
20-49 |
750 mg Q48H |
500 mg x1, then 250 mg Q24H |
250 mg Q24H |
|
10-19 |
750 mg x 1, then 500 mg Q48H |
500 mg x1, then 250 mg Q48H |
250 mg Q48H |
|
Hemodialysis/CAPD |
750 mg x1, then 500 mg Q48H |
500 mgx1, then 250 mg Q48H |
|
|
| Lidocaine & Tetracaine Patch Patch |
Lidocaine & Tetracaine
Patch (Synera) P&T, is recommended for
addition to SMH formulary, to be made available for relief of pain for
superficial venous access and dermatologic procedures; restricted to pediatric
patients at least 3 years of age. |
| Linezolid |
Linezolid is
restricted to VRE
Linezolid is
restricted for treatment of documented serious vancomycin resistant
Enterococcus faecium infections when no other alternative is available.
Doxycycline
and nitrofurantoin are recommended for susceptible VRE lower urinary tract
infections.
Linezolid is
not recommended for treatment of other documented infections unless the patient
is allergic/intolerant to all other antibiotics demonstrating activity against
the pathogen.
|
| Lisopro |
Autosubstitute with
Novolog
unit for unit
·
Novolog
(insulin aspart) will be auto-substituted for Humalog (Lispro) as the onset and
duration are similar and Novolog is less expensive.
|
|
Loratadine Tablet |
Loratadine (Claritinâ)
and Claritin D 12 hour (5 mg with 120 of pseudoephedrine) are the P&T
recommended formulary non-sedating antihistamines with automatic substitution
for desloratadine (Clarinexâ)
fexofenadine (Allegraâ
30, 60, 180 mg), Allegra Dâ
(60 mg fexofenadine with 120 mg pseudoephedrine), Allegra D 24 Hourâ
(180 mg fexofenadine and 240 mg pseudoephedrine), cetirizine (Zyrtecâ),
and Semprex D (8 mg acrivastine with 60 mg pseudoephedrine). They will be
stocked in the following dosage forms: Claritin 10 mg, Clartin D 12 hour, and as
the syrup 1 mg/ml for pediatric patients.
P&T/MEC APPROVED 11/2000,
updated 3/21/07
|
Non Formulary Medication Ordered |
P&T/MEC Approved Auto Substitution |
|
Allegra 30 mg every day, 6-11 years old
with renal dysfunction |
|
|
Allegra 30 mg BID, 6-11 years old |
Claritin 10 mg every
day |
|
Allegra 60 mg every day, 12 years and
older with renal dysfunction |
Claritin 10 mg every
other day |
|
Allegra 60 mg BID, 12 years and older |
Claritin 10 mg every
day |
|
Allegra 180 mg every day, 12 years and
older |
Claritin 10 mg every
day |
|
Allegra D one every 12 hours, 12 years and
older |
Claritin D one every
12 hours |
|
Allegra D 24H every day |
Claritin D one every
12 hours |
|
|
|
|
Clarinex 5 mg every other day, 12 years
and older: Clcr < 30 ml/min or liver impairment |
Claritin 10 mg every
other day |
|
Clarinex 5 mg every day, 12 years and
older |
Claritin 10 mg every
day |
|
|
|
|
Zyrtec 2.5 mg every day, 6 months to < 2
years
Maximum dose: 2.5 mg every 12 hours |
Do not substitute
for patients < 2 years |
|
Zyrtec 2.5 mg every day, 2-5 years old
Maximum 2.5 mg every 12 hours or 5 mg once
daily |
Claritin 5 mg every
day |
|
Zyrtec 5 mg every day, 6-11 years old:
clcr < 31 ml/min, on hemodialysis or hepatically impaired |
Claritin 10 mg every
other day |
|
Zyrtec 5–10 mg every day, 6-11 years old |
Claritin 10 mg every
day |
|
Zyrtec 5 mg every day, 12 years and older:
clcr < 31 ml/min, on hemodialysis or hepatically impaired |
Claritin 10 mg every
other day |
|
Zyrtec 5-10 mg every day, 12 years and
older |
Claritin 10 mg every
day |
*Note Claritin dosage in renal
impairment, clcr < 30 ml/min, or hepatic failure: 2-5 years old 5 mg every other
day, 6 years and older 10 mg every other day. |
| Lubiprostone (Amitiza®) |
Package Insert;
this product has a high incidence of nausea (31%), diarrhea
(13.2%), and vomiting (4.6%). It is non-formulary and it is not recommended to
be initiated in the hospital, but may be used as a continuation of therapy from
home. |
| |
|
|