ATTENTION: Aspiring, New, and Retail Pharmacy Technicians
Do you want to learn....
"How To Transition From A Retail Pharmacy To A Compounding Pharmacy Setting Without Experience Or Formal Training"
Say YES. I'm ready to Make more than what retail pharmacy technicians make.
Say YES. I still want to be in the pharmacy or medical field but, I DON'T WANT the responsibility of talking or interacting with angry patients, and
Say YES. I want to be in a fun, more relaxed pharmacy setting while "making something" for my patients.
ATTENTION: Aspiring, New, and Retail Pharmacy Technicians
Do you want to learn....
"How To Transition From A Retail Pharmacy To A Compounding Pharmacy Setting Without Experience Or Formal Training"
Say YES. I'm ready to Make more than what retail pharmacy technicians make.
Say YES. I still want to be in the pharmacy or medical field but, I DON'T WANT the responsibility of talking or interacting with angry patients, and
Say YES. I want to be in a fun, more relaxed pharmacy setting while "making something" for my patients.
If You Act Now, You get a Lifetime Access to "Non-sterile Compounding Techniques Certification", including:
* The General Chapters of USP that pertain to compounding -
So
To Your Success,Prof. Lorraine LohnerP.S. - Every minute you wait to get "Non-sterile Compounding Techniques Certification" is another minute other pharmacy technicians will get further ahead of you and have more fun being pharmacy technicians.Disclaimer: This is not the official This course is for review or study guide purposes only. For official USP 795 information, go to the USP website.
Weighing
It is generally agreed that pharmaceutical products should be prepared with a low percentage of error. The official compendia allow a tolerance of ± 5% for most formulas, although greater accuracy may be required for very potent drugs with greater toxicity potential. This same degree of accuracy is expected in all extemporaneously compounded products.
Most pharmaceutical products allow for a tolerance of only 5% error, where

If we know the sensitivity of the balance (i.e. the potential error) we can calculate the percentage of possible error when any amount of the substance is weighed.
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e.g. The Class III prescription balance has a sensitivity of 6 mg. What % of error would result in weighing 50 mg of a drug on the balance?

Similarly, we can calculate the smallest quantity that can be weighed, on a balance of known sensitivity, to maintain a desired level of accuracy. This weight is referred to as the least weighable quantity (L.W.Q.).

e.g. What is the least weighable quantity that will result in an error of 5% or less on a Class III prescription balance?

You should keep this figure in mind for the remainder of your career. When a prescription formula calls for the incorporation of a component weighing less than 120 mg, special methods must be employed to obtain that weight of the component. If a liquid dosage form (solution, suspension or emulsion) is being prepared, the liquid aliquot method is employed. When the component must be incorporated as a solid into powders, tablets, capsules, or pastes, the trituration method is used.
Reference: https://pharmlabs.unc.edu/labs/measurements/weigh.htm
Trituration Method
A trituration is a dilution of a potent drug powder with an inert diluent powder, usually lactose, in a definite proportion by weight. We can then remove a weighable portion (aliquot) of the mixture containing the desired quantity of substance to maintain an acceptable range of accuracy.
Using ratio and proportion, we can determine the weight of drug and lactose required to make the trituration as well as the weight of the aliquot to be used to fill the prescription.

Keep in mind that any substance that must be weighed on the balance drug (A), lactose (B-A), and aliquot (D) must be at least 120 mg.
Lactose is the most commonly used diluent in solid dosage form pharmaceuticals such as powders, tablets and capsules. Some of the reasons included its extremely low incidence of side effects, ready availability, and low cost.
Example: Make 10 capsules, each containing 0.6 mg Atropine Sulfate and each weighing a total of 200 mg.
1. Total weight atropine sulfate required (this is C in the proportion)

2. Select some multiple of 6 mg that can be weighed with the desired degree of accuracy. (this is A in the proportion) (e.g. select multiple= 20)

3. Select the size of the aliquot portion to be taken to contain the 6 mg of drug. (this is D in the proportion)

4. Since we now have A, C, and D in our formula, we can solve for B(trituration weight).

[Note: this should be the multiple (20) x the weight of the aliquot (120 mg)]
5. Determine the weight of diluent (lactose) required to prepare the trituration by subtracting the weight of atropine sulfate from the trituration weight.

6. Fill Rx:
Determine the weight of lactose which must be added to the aliquot portion of trituration to complete the prescription, so that each capsule weighs 200 mg.

After the necessary calculations are completed, the trituration is prepared using the following steps:
Hence the compounding procedure for this product is as follows:
Remove 120 mg of the trituration (contains 6 mg atropine sulfate) (Hint: save left over trituration for refills)
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