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U.S. Health Coalition message: "Double Check, Don't Double Up" is in reference to which of the following?

a. Acetaminophen
b. Digoxin
c. Levothyroxine
d. Oxycodone

Answer: 


U.S. Health Coalition message: "Double Check, Don't Double Up" is in reference to which of the following?

a. Acetaminophen
b. Digoxin
c. Levothyroxine
d. Oxycodone

Answer: Acetaminophen. The Acetaminophen Awareness Coalition is launching a nationwide initiative today calling on consumers to double check their medicine labels so they don't double up on medicines that contain acetaminophen during the cold and flu season. Acetaminophen is the most common drug ingredient in America. It is found in more than 600 different medicines, including prescription (Rx) and over-the-counter (OTC) pain relievers, fever reducers, sleep aids and numerous cough, cold and flu medicines. It is safe and effective when used as directed, but there is a limit to how much can be taken in one day. Taking more than directed is an overdose and can lead to liver damage.

Each year, Americans catch an estimated one billion colds, and as many as 20 percent get the flu. Seven in 10 consumers use over-the-counter medicines, many of which contain acetaminophen, to treat their symptoms. The Coalition is targeting its "Double Check, Don't Double Up" message to the more than 50 million Americans who use acetaminophen weekly for conditions such as headache and chronic pain, and directing them to double check their medicine labels before taking a cold or flu medicine that also contains acetaminophen.

When taking medicines for cough, cold or flu this coming season, consumers should follow these four simple acetaminophen safety steps:

1. Know if medicines contain acetaminophen, which is in bold type or highlighted in the "active ingredients" section of over-the-counter medicine labels and sometimes listed as "APAP" or "acetam" on prescription labels.
2. Never take two medicines that contain acetaminophen at the same time.
3. Always read and follow the medicine label.
4. Ask your healthcare provider or a pharmacist if you have questions about dosing instructions or medicines that contain acetaminophen.


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Which of the following statements is/are TRUE ABOUT Palforzia? [Select ALL THAT APPLY]

a. The active ingredient found in Palforzia is Arachis hypogaea.
b. It is indicated to prevent peanut hypersensitivity.
c. It indicated for the emergency treatment of allergic reactions, including anaphylaxis.
d. It should not be administered in patients with uncontrolled asthma.
e. It is available only through a restricted program Palforzia REMS.


Which of the following statements is/are TRUE ABOUT Palforzia? [Select ALL THAT APPLY]

a. The active ingredient found in Palforzia is Arachis hypogaea.
b. It is indicated to prevent peanut hypersensitivity.
c. It indicated for the emergency treatment of allergic reactions, including anaphylaxis.
d. It should not be administered in patients with uncontrolled asthma.
e. It is available only through a restricted program Palforzia REMS.

Answer: (a,b,d,e). The active ingredient found in Palforzia is (Peanut (Arachis hypogaea) Allergen Powder-dnfp). It is an oral immunotherapy indicated for the mitigation of allergic reactions, including anaphylaxis, that may occur with accidental exposure to peanut. Palforzia is approved for use in patients with a confirmed diagnosis of peanut allergy.

Palforzia can cause anaphylaxis, which may be life-threatening and can occur at any time during Palforzia therapy. It is NOT indicated for the emergency treatment of allergic reactions, including anaphylaxis.

Prescribe injectable epinephrine, instruct and train patients on its appropriate use, and instruct patients to seek immediate medical care upon its use.

Do not administer Palforzia to patients with uncontrolled asthma. Observe patients during and after administration of the Initial Dose Escalation and the first dose of each Up-Dosing level, for at least 60 minutes.

Palforzia is available only through a restricted program called the Palforzia REMS.


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In a patient taking Erythromycin, the dose of Livalo should be restricted to:
 
a. 1 mg per day.
b. 5 mg per day.
c. 10 mg per day.
d. 25 mg per day.
e. 50 mg per day.


In a patient taking Erythromycin, the dose of Livalo should be restricted to:
 
a. 1 mg per day.
b. 5 mg per day.
c. 10 mg per day.
d. 25 mg per day.
e. 50 mg per day.
 
Answer: a. Pitavastatin (Livalo) is an inhibitor of HMG-CoA reductase. It is a synthetic lipid-lowering agent for oral administration. Each film-coated tablet of Pitavastatin (Livalo) contains1 mg. 2 mg or 4 mg Pitavastatin.
 
It is indicated as an adjunctive therapy to diet to reduce elevated total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (Apo B), triglycerides (TG), and to increase HDL-C in adult patients with primary hyperlipidemia or mixed dyslipidemia.
 
Doses of Pitavastatin (Livalo) greater than 4 mg once daily were associated with an increased risk for severe myopathy in premarketing clinical studies. PAtients should not exceed 4 mg once daily dosing of Pitavastatin (Livalo). The dose range for Pitavastatin (Livalo) is 1 to 4 mg orally once daily at any time of the day with or without food. The recommended starting dose is 2 mg and the maximum dose is 4 mg.
 
In patients taking erythromycin, a dose of Pitavastatin (Livalo) 1 mg once daily should not be exceeded. In patients taking rifampin, a dose of Pitavastatin (Livalo) 2 mg once daily should not be exceeded.
 
Rhabdomyolysis with myoglobinuria and acute renal failure and myopathy (including myositis) and liver enzyme abnormalities are principal side effects of Pitavastatin (Livalo).
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Ofirmev, available as an injection, is an antipyretic and non-opioid analgesic agent. Which of the following is an active ingredient found in it?
 
a. Acetaminophen
b. Ibuprofen
c. Tramadol
d. Aspirin
e. Pregabalin


Ofirmev, available as an injection, is an antipyretic and non-opioid analgesic agent. Which of the following is an active ingredient found in it?
 
a. Acetaminophen
b. Ibuprofen
c. Tramadol
d. Aspirin
e. Pregabalin
 
Answer: a
 
Acetaminophen (Ofirmev) is a non-salicylate antipyretic and non-opioid analgesic agent in injection dosage form. It is indicated for:

1. the management of mild to moderate pain;
2. the management of moderate to severe pain with adjunctive opioid analgesics;
3. the reduction of fever.
 
Acetaminophen (Ofirmev) may be given as a single or repeated dose for the treatment of acute pain or fever. No dose adjustment is required when converting between oral acetaminophen and Acetaminophen (Ofirmev) dosing in adults and adolescents. The maximum daily dose of acetaminophen is based on all routes of administration (i.e. intravenous, oral, and rectal) and all products containing acetaminophen.
 
Adults and adolescents weighing 50 kg and over: the recommended dosage of Acetaminophen (Ofirmev) is 1000 mg every 6 hours or 650 mg every 4 hours, with a maximum single dose of Acetaminophen (Ofirmev) of 1000 mg, a minimum dosing interval of 4 hours, and a maximum daily dose of acetaminophen of 4000 mg per day.
 
Adults and adolescents weighing under 50 kg: the recommended dosage of Acetaminophen (Ofirmev) is 15 mg/kg every 6 hours or 12.5 mg/kg every 4 hours, with a maximum single dose of Acetaminophen (Ofirmev) of 15 mg/kg, a minimum dosing interval of 4 hours, and a maximum daily dose of acetaminophen of 75 mg/kg per day.


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Patients should be advised to report immediately which of the following signs or symptoms when on Clozapine therapy? [Select ALL THAT APPLY].

a. Lethargy
b. Fever
c. Sore throat
d. Weakness
e. Severe nausea and vomiting


Patients should be advised to report immediately which of the following signs or symptoms when on Clozapine therapy? [Select ALL THAT APPLY].

a. Lethargy
b. Fever
c. Sore throat
d. Weakness
e. Severe nausea and vomiting

Answer: (a,b,c,d). Clozaril (Clozapine), an atypical antipsychotic drug, is indicated for:

1. Treatment-Resistant Schizophrenia
2. Reduction in the Risk of Recurrent Suicidal Behavior in Schizophrenia or Schizoaffective Disorders

Because of a significant risk of agranulocytosis, a potentially Life-threatening adverse event, Clozaril (Clozapine) should be Reserved for use in

(1). the treatment of severely ill patients with Schizophrenia who fail to show an acceptable response to Adequate courses of standard antipsychotic drug treatment,

Or

(2). for reducing the risk of recurrent suicidal behavior in patients With schizophrenia or schizoaffective disorder who are judged to Be at risk of reexperiencing suicidal behavior.
Patients being treated with Clozapine must have a baseline white Blood cell (WBC) count and absolute neutrophil count (ANC) before initiation of treatment as well as regular WBC counts and ANCs during treatment and for at least 4 weeks after Discontinuation of treatment.

Clozapine is available only through a distribution system that Ensures monitoring of WBC count and ANC according to the Schedule described below prior to delivery of the next supply of Medication.

Agranulocytosis, defined as an ANC of less than 500/mm3, has been reported with Clozaril (Clozapine). Patients should be advised to report immediately the appearance of lethargy, weakness, fever, sore throat or any other signs of infection occurring at any time during Clozaril (Clozapine) therapy. Such patients should have a WBC count and ANC performed promptly.


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Nymalize, a calcium channel blocker, is indicated for which of the following?
 
a. Hypertension
b. Arrhythmia
c. Parkinson's
d. Subarachnoid hemorrhage
e. Depression


Nymalize, a calcium channel blocker, is indicated for which of the following?
 
a. Hypertension
b. Arrhythmia
c. Parkinson's
d. Subarachnoid hemorrhage
e. Depression

Answer:d.

Nymalize contains Nimodipine, a dihydropyridine calcium channel blocker. An oral solution of Nymalize contains 60 mg of Nimodipine per 20 mL.

It is indicated for the improvement of neurological outcome by reducing the incidence and severity of ischemic deficits in adult patients with subarachnoid hemorrhage (SAH) from ruptured intracranial berry aneurysms regardless of their post-ictus neurological condition (i.e., Hunt and Hess Grades I-V).

The recommended oral dosage is 20 mL (60 mg) every 4 hours for 21 consecutive days.

Hypotension is the major side effect of Nymalize.


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Khedezla is indicated for the treatment of which of the following?...


Khedezla is indicated for the treatment of which of the following?

a. Hypertension
b. Depression
c. Arthritis
d. Type II diabetes
e. Parkinsons

Answer: (b) Depression

The active ingredient found in Khedezla is Desvenlafaxine. Desvenlafaxine (O-desmethylvenlafaxine) is the major active metabolite of the antidepressant Effexor (Venlafaxine), a medication used to treat major depressive disorder.
 
Khedezla contains the serotonin and norepinephrine reuptake inhibitor (SNRI) Desvenlafaxine, which is also contained in Pristiq. Pristiq was approved by the FDA in 2008 and contains Desvenlafaxine as the succinate salt.
 
Khedezla will be available in 50 mg and 100 mg strengths for once daily administration. The recommended dose for Khedezla is 50 mg once daily, with or without food. It should be taken at approximately the same time each day. Tablets must be swallowed whole with fluid and not divided, crushed, chewed, or dissolved.
 
In clinical studies, doses of 50 mg to 400 mg per day were shown to be effective, although no additional benefit was demonstrated at doses greater than 50 mg per day and adverse reactions and discontinuations were more frequent at higher doses.
 
Nausea, dizziness, insomnia, hyperhidrosis (excessive sweating), constipation, drowsiness, decreased appetite, anxiety, and specific male sexual function disorders are commonly reported side effects of the drug.
 


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Based on the genetic make-up of SARS-CoV-2, which of the following drug classes is most likely to prove effective?

a. Angiotensin converting enzyme inhibitors
b. Protease inhibitors
c. Nucleoside analogues
d. Neuraminidase inhibitors
e. Calcium channel blockers


Based on the genetic make-up of SARS-CoV-2, which of the following drug classes is most likely to prove effective?

a. Angiotensin converting enzyme inhibitors
b. Protease inhibitors
c. Nucleoside analogues
d. Neuraminidase inhibitors
e. Calcium channel blockers

Answer: (b). The SARS-CoV-2 RNA codes for a pair of protease enzymes that are essential to production of viable virions upon release. Since protease inhibitors have been highly effective for treating patients with infections of human immunodeficiency virus and hepatitis C virus, that is the best choice.

Use of neuraminidase inhibitors (e.g., oseltamivir, peramivir, zanamivir) is not logical, since coronaviruses do not have a gene for neuraminidase.

Nucleoside analogues (e.g., acyclovir, ganciclovir, ribavirin) would be expected to exert effects only at high levels since the coronavirus has an exonuclease that would recognize and remove the analogues when incorporated into the viral genome.

It is currently unknown as to whether angiotensin converting enzyme (ACE) inhibitors or angiotensin-2 receptor blockers (ARBs) are beneficial or harmful based on changes in the ACE2 protein involved in viral entry in lung tissue.



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The recommended dose of Olumiant in patients taking strong Organic Anion Transporter 3 (OAT3) inhibitors is _____________.

a. 1 mg once daily
b. 2 mg once daily
c. 3 mg once daily
d. 4 mg once daily
e. Cannot be used with OAT3 inhibitors


The recommended dose of Olumiant in patients taking strong Organic Anion Transporter 3 (OAT3) inhibitors is _____________.

a. 1 mg once daily
b. 2 mg once daily
c. 3 mg once daily
d. 4 mg once daily
e. Cannot be used with OAT3 inhibitors

Answer: (a). The active ingredient found in Olumiant is Baricitinib. It is a Janus kinase (JAK) inhibitor indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more TNF antagonist therapies.

1. The recommended dose of Olumiant (Baricitinib) in patients taking strong Organic Anion Transporter 3 (OAT3) inhibitors (e.g., probenecid) is 1 mg once daily.

2. The recommended dose of Olumiant (Baricitinib) in patients with moderate renal impairment is 1 mg once daily.

3. Olumiant (Baricitinib) is not recommended in patients with severe renal impairment.

4. Olumiant (Baricitinib) is not recommended in patients with severe hepatic impairment.

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Which of the following statements would indicate that a patient understands why he is taking Olumiant?

a. "I have vasomotor symptoms associated with menopause."
b. "I have rheumatoid arthritis."
c. "I have hypercalcemia."
d. "I have Paget's disease of bone."
e. "I have migraine headaches associated with menopause."


Which of the following statements would indicate that a patient understands why he is taking Olumiant?

a. "I have vasomotor symptoms associated with menopause."
b. "I have rheumatoid arthritis."
c. "I have hypercalcemia."
d. "I have Paget's disease of bone."
e. "I have migraine headaches associated with menopause."

Answer: b

The active ingredient found in Olumiant is Baricitinib. It is a Janus kinase (JAK) inhibitor indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more TNF antagonist therapies.

The recommended dose of Olumiant is 2 mg once daily.

Upper respiratory tract infections, nausea, herpes simplex, and herpes zoster are commonly reported side effects of the drug.

The drug also has shown promising result for the treatment of Covid-19 infection when administered simultaneously with Remdesivir.Olumiant (Baricitinib) in combination with Veklury (Remdesivir) cuts the median recovery time by about a day, compared to patients treated with Remdesivir alone.




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