Anurse is caring for a patient who is on amphotericin b. on morning rounds the patient reports weakness, numbness, and a tingling sensation in his feet. what would be a priority action by the nurse?

Amphotericin treats problems like fatal fungal infection.

Further Explanation:

Amphotericin is a type of drug used to treat problems like fatal fungal infection. It stops the growth of fungi. Fungi is the multicellular organism that are heterotrophic in nature which means they feed on other organism. There are some fungi which are edible but some are very harmful to the human beings.

The amphotericin-b is injected into body through the veins. It is given slowly through the intravenous infusion depending on the severity of the infection the amphotericin-B can be given upto many weeks or months.

The common side effect of the drug may include: vomiting, stomach ache, nausea, headache, joint pain, diarrhea and weight loss.

If the patient who has been taking amphotericin reports weakness, numbness, and a tingling sensation in his feet then he might be suffering from sensory disturbances. The nurse should help the patient when they get out of the bed and in order to prevent the risk of infection they should use the aseptic technique.

Learn more:

1. Learn more about hormone

2. Learn more about reproduction

3. Learn more about lymphatic system

Answer details:

Grade: College biology

Subject: Biology

Chapter: Hormones

Keywords:

Amphotericin, fungal infection, fungi, vomiting, stomach ache, nausea,, headache,, joint pain, diarrhea, weight loss, aseptic technique.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.