Buy 5 or More Products! Save 25% On Total.
 Buy 3 or More Products! Save 10% On Total.
 Free Shipping! No Minimum Order.



Blog Empty Image

Which of the following information is/are TRUE about preparing TPN formulation? (Select All that apply).
 
a. A lipid emulsion in a three-in-one admixture obscures the presence of calcium phosphate precipitates.
b. The solubility of the added calcium should be calculated from the volume at the time the calcium is added and should NOT be based upon the final volume.
c. If the amount of calcium or phosphate which must be added is likely to cause a precipitate, some or all of the calcium should be administered separately.
d. If a three-in-one admixture is medically necessary, then add the calcium before the lipid emulsion.
e. When adding calcium and phosphate to an admixture, the calcium should be added first.


Which of the following information is/are TRUE about preparing TPN formulation? (Select All that apply).
 
a. A lipid emulsion in a three-in-one admixture obscures the presence of calcium phosphate precipitates.
b. The solubility of the added calcium should be calculated from the volume at the time the calcium is added and should NOT be based upon the final volume.
c. If the amount of calcium or phosphate which must be added is likely to cause a precipitate, some or all of the calcium should be administered separately.
d. If a three-in-one admixture is medically necessary, then add the calcium before the lipid emulsion.
e. When adding calcium and phosphate to an admixture, the calcium should be added first.

Answer: (a,b,c,d). TPN solutions are made according to a variety of formulations and compounding protocols. Thus, there are possibilities of calcium phosphate precipitates and many other chemical incompatibilities. Precipitates could develop because of a number of factors such as: the concentration, pH, and phosphate content of the amino acid solutions; the calcium and phosphorous additives; the order of mixing; the mixing process; or the compounder. The presence of a lipid emulsion in the TPN admixture would obscure the presence of any precipitate.
 
Because of the potential for life threatening events, caution should be taken to ensure that precipitates have not formed in any parenteral nutrition admixtures.
 
1. The amounts of phosphorous and of calcium added to the admixture are critical. The solubility of the added calcium should be calculated from the volume at the time the calcium is added. It should not be based upon the final volume.
 
Some amino acid injections for TPN admixtures contain phosphate ions (as a phosphoric acid buffer). These phosphate ions and the volume at the time the phosphate is added should be considered when calculating the concentration of phosphate additives. Also, when adding calcium and phosphate to an admixture, the phosphate should be added first. 
 
2. The line should be flushed between the addition of any potentially incompatible components.
 
3. A lipid emulsion in a three-in-one admixture obscures the presence of a precipitate. Therefore, if a lipid emulsion is needed, either:

(1). use a two-in-one admixture with the lipid infused separately, or
(2). if a three-in-one admixture is medically necessary, then add the calcium before the lipid emulsion and according to the recommendations in number 1 above.
 
If the amount of calcium or phosphate which must be added is likely to cause a precipitate, some or all of the calcium should be administered separately. Such separate infusions must be properly diluted and slowly infused to avoid serious adverse events related to the calcium.

4. A filter should be used when infusing either central or peripheral parenteral nutrition admixtures. Standards of practice vary, but the following is suggested: a 1.2 micron air eliminating filter for lipid containing admixtures, and a 0.22 micron air eliminating filter for nonlipid containing admixtures.


Blog Empty Image

Prescribing authority shall be allowed, under the medical direction of a supervising physician, for:
 
I. Advanced registered nurse practitioners.
II. Clinical nurse specialists  
III. Certified nurse-midwives.

a. I only
b. I and II only
c. II and III only
d. All


Prescribing authority shall be allowed, under the medical direction of a supervising physician, for:
 
I. Advanced registered nurse practitioners.
II. Clinical nurse specialists  
III. Certified nurse-midwives.
 
a. I only
b. I and II only
c. II and III only
d. All

Answer: All, [Title 59 Oklahoma Pharmacy Act Chapter 8 Section 353.1a]. 
 
Prescribing authority shall be allowed, under the medical direction of a supervising physician, for an advanced practice nurse recognized by the Oklahoma Board of Nursing in one of the following categories: advanced registered nurse practitioners, clinical nurse specialists, or certified nurse-midwives.
 
The advanced practice nurse may write or sign, or transmit by word of mouth, telephone or other means of communication an order, for drugs or medical supplies that is intended to be filled, compounded, or dispensed by a pharmacist.
 
The supervising physician and the advanced practice nurse shall be identified at the time of origination of the prescription and the name of the advanced practice nurse shall be printed on the prescription label.

 


Blog Empty Image

According to Oklahoma State Pharmacy Law, every registered pharmacist or assistant pharmacist shall, within ten (10) days after discontinuing or changing his or her place of practice, remove his or her certificate and notify the Executive Director of the Board of his or her new place of practice.

True or False


According to Oklahoma State Pharmacy Law, every registered pharmacist or assistant pharmacist shall, within ten (10) days after discontinuing or changing his or her place of practice, remove his or her certificate and notify the Executive Director of the Board of his or her new place of practice.
 
Answer: True, [Title 59 Oklahoma Pharmacy Act Chapter 8 Section 353.12(A)].
 
Every person upon receiving a certificate of licensure pursuant to the Oklahoma Pharmacy Act, or who has heretofore received a certificate of licensure in this state, shall keep such certificate conspicuously displayed in the pharmacy where such pharmacist is actively engaged in the practice of pharmacy or in such a location as is otherwise prescribed by the State Board of Pharmacy.
 
The current receipt for licensure shall be attached to the lower left corner of the original certificate.
 
According to Oklahoma State Pharmacy Law, every registered pharmacist or assistant pharmacist shall, within ten (10) days after discontinuing or changing his or her place of practice, remove his or her certificate and notify the Executive Director of the Board of his or her new place of practice.


Blog Empty Image

Which of the following vaccines is required to be stored in a freezer?
 
a. Hepatitis A
b. Human papilloma virus
c. Influenza
d. Herpes Zoster


Which of the following vaccines is required to be stored in a freezer?
 
a. Hepatitis A
b. Human papilloma virus
c. Influenza
d. Herpes Zoster

Answer: Herpes zoster.

The following vaccines are required to be stored in refrigerator (2 to 8 degree C):

1. HepA (Hepatitis A)
2. HepB (Hepatitis B)
3. Hib (Haemophilus influenzae type b)
4. HPV (Human papilloma virus)
5. Influenza
6. Meningococcal-combinations
7. Pneumococcal
8. Rotavirus
9. Any diphtheria/tetanus toxoid, pertussis combination
 
The following vaccines are required to be stored in freezer (-50 to -15 degrees C):

1. VAR (Varicella)
2. HZV (Herpes Zoster Vaccine)
3. MMRV = Measles, mumps, rubella, varicella
 
The following vaccines can be stored in refrigerator (2 to 8 degree C) or freezer (-50 to -15 degrees C):

1. MMR (Measles, mumps, rubella)


Clobazam is classified as a:
 
a. Schedule II controlled drug
b. Schedule III controlled drug
c. Schedule IV controlled drug
d. Schedule V controlled drug
 


Clobazam is classified as a:
 
a. Schedule II controlled drug
b. Schedule III controlled drug
c. Schedule IV controlled drug
d. Schedule V controlled drug
 
Answer: (c). The active ingredient found in Onfi is Clobazam. It is classified as schedule IV controlled substance. Each Onfi (Clobazam) tablet contains 10 mg or 20 mg of clobazam. It is also available for oral administration as an off-white suspension containing clobazam at a concentration of 2.5 mg/mL.
 
Onfi (Clobazam) is classified as benzodiazepine. Clobazam potentiates the GABAergic neurotransmission by binding at the benzodiazepine site of the GABAa receptor.
 
Onfi (Clobazam) is indicated for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years of age or older.
 
A daily dose of Onfi (Clobazam) greater than 5 mg should be administered in divided doses twice daily; a 5 mg daily dose can be administered as a single dose.
 
As with all antiepileptic drugs and benzodiazepines, withdraw Onfi (Clobazam) gradually. The patient should taper by decreasing the total daily dose by 5-10 mg/day on a weekly basis until discontinued.
 
Somnolence, depression, sedation, withdrawal symptoms, serious dermatological reactions and suicidal behavior and ideation are commonly reported side effects of Onfi (Clobazam).
 
www.pharmacyexam.com


Blog Empty Image

Coming at a time when heroin and opioid overdoses are gripping the nation, a new Colorado law allows pharmacies to sell naloxone without a prescription. A number of states are allowing measures like Colorado’s to combat increasing overdose death rates associated with prescription opioid and heroin abuse.
 
NABP’s AWARXE® Prescription Drug Safety Program is working to reduce opioid and heroin overdose deaths by educating the public on prescription drug abuse and misuse. The program’s website offers resources such as facts on the dangers of prescription drug abuse, informational flyers and posters, and a Locator Tool to help consumers find prescription drug disposal programs near them.


Coming at a time when heroin and opioid overdoses are gripping the nation, a new Colorado law allows pharmacies to sell naloxone without a prescription. A number of states are allowing measures like Colorado’s to combat increasing overdose death rates associated with prescription opioid and heroin abuse.
 
NABP’s AWARXE® Prescription Drug Safety Program is working to reduce opioid and heroin overdose deaths by educating the public on prescription drug abuse and misuse. The program’s website offers resources such as facts on the dangers of prescription drug abuse, informational flyers and posters, and a Locator Tool to help consumers find prescription drug disposal programs near them.


Blog Empty Image

Which of the following drugs utilizes ZipDose Technology?

a. Olanzapine
b. Metoprolol
c. Levetiracetam
d. Fluoxetine
e. Amoxicillin


Which of the following drugs utilizes ZipDose Technology?

a. Olanzapine
b. Metoprolol
c. Levetiracetam
d. Fluoxetine
e. Amoxicillin

Answer: Levetiracetam. Levetiracetam (Spritam) is indicated for the treatment of partial onset seizures, myoclonic seizures and primary generalized tonic-clonic seizures in adults and children with epilepsy.
 
Spritam utilizes Aprecia's proprietary ZipDose® Technology platform, a groundbreaking advance that uses three-dimensional printing (3DP) to produce a porous formulation that rapidly disintegrates with a sip of liquid.1 While 3DP has been used previously to manufacture medical devices, this approval marks the first time a drug product manufactured with this technology has been approved by the FDA.
 
ZipDose Technology enables the delivery of a high drug load, up to 1,000 mg in a single dose. As a result, Spritam enhances the patient experience - administration of even the largest strengths of Levetiracetam (Spritam) with just a sip of liquid. In addition, with Spritam there is no measuring required as each dose is individually packaged, making it easy to carry this treatment on the go.
 
The recommended daily dose is 1000 to 3000 mg per day.
 
Sleepiness, weakness, dizziness, infection, tiredness, acting aggressive, nasal congestion, decreased appetite, and irritability are commonly reported side effects of Levetiracetam (Spritam).
 
Levetiracetam is also available under the trade names Keppra and Elepsia.




Free USA Shipping! No Minimum Order.
Free International Shipping! Over $350 or More.