Drug Study
Drug Study
Drug Study
ACTION EFFECTS
GENERIC NAME: Description: Clindamycin is Hypersensitivity hardness, pain, or a Followed the 10
Nalbuphine is a indicated in the soft, painful bump in Rights of Drug
phenanthrene treatment of serious the area where Administration.
BRAND NAME: derivative w/ mixed infections, when clindamycin was Assess dizziness
opioid agonist and caused by injected that might affect
antagonist activity clindamycin unpleasant or gait, balance, and
PATIENT’S DOSE: (agonist at kappa susceptible strains metallic taste in the other functional
opiate receptor; partial of gram-positive mouth activities.
antagonist at μ aerobes such as nausea Use appropriate
ROUTE OF receptor). It inhibits the streptococci, vomiting pain scales (visual
ADMINISTRATION: ascending pain pneumococci and joint pain analogue scales,
pathways, alters the staphylococci, or by white patches in the others) to
perception of and susceptible mouth document
CLASSIFICATION: response to pain by anaerobic bacteria thick, white vaginal whether this drug
binding to opiate discharge is successful in
receptors in the CNS. It burning, itching, and helping manage
also produces swelling of the the patient's pain.
generalised CNS vagina Help patient
depression. explore other
Onset: 2-3 min (IV); nonpharmacologic
<15 min (IM/SC). methods to
Duration: 3-6 hr. reduce chronic
Pharmacokinetics: pain, such as
Absorption: Time to relaxation
peak plasma techniques,
concentration: 30 min exercise,
(IM). counseling, and
Distribution: Crosses so forth.
the placenta and Monitor patient
distributed in breast response to
milk (small amounts). therapy
Plasma protein binding: Monitor for
Approx 50%. adverse effects
Metabolism: Monitor patient
Undergoes extensive compliance to
first-pass metabolism in drug therapy.
GI mucosa and liver.
Excretion: Via urine
and faeces (as
unchanged drug and
conjugates). Elimination
half-life: 5 hr