PHARMACOLOGY
PHARMACOLOGY
PHARMACOLOGY
Aside from their analgesic, antipyretic and anti-inflammatory effects, they also
decrease platelet aggregation which is useful in preventing conditions caused by
thromboembolism such as transient ischemic attacks, myocardial infarction, and
stroke.
NSAIDs work by inhibiting the activity of cyclooxygenase enzymes (the COX-1 and
COX-2 isoenzymes). In cells, these enzymes are involved in the synthesis of key
biological mediators, namely prostaglandins, which are involved in inflammation,
and thromboxane, which are involved in blood clotting.
There are two general types of NSAIDs available: non-selective, and COX-2
selective. Most NSAIDs are non-selective, and inhibit the activity of both COX-1
and COX-2. These NSAIDs, while reducing inflammation, also inhibit platelet
aggregation and increase the risk of gastrointestinal ulcers and bleeds. COX-2
selective inhibitors have fewer gastrointestinal side effects, but promote
thrombosis, and some of these agents substantially increase the risk of heart
attack.
Actions of NSAIDs
The inhibition of prostaglandin biosynthesis is the main mechanism for the anti-
inflammatory and analgesic effect of NSAIDs. They block the cyclooxygenase thus
preventing arachidonic acid from synthesizing prostaglandins. Arachidonic acid is
liberated when there is cell membrane damage during inflammation.
They are classified based on their chemical structures with each category having
slightly different characteristics.
Gastrointestinal
NSAID the acidic molecules directly irritate the gastric mucosa, and inhibition of
COX-1 and COX-2 reduces the levels of protective prostaglandins. Inhibition of
prostaglandin synthesis in the GI tract causes increased gastric acid secretion,
diminished bicarbonate secretion, diminished mucus secretion and diminished
trophic effects on the epithelial mucosa.
Renal
NSAIDs are also associated with a fairly high incidence of adverse drug reactions
(ADRs) on the kidney and over time can lead to chronic kidney disease. The
mechanism of these kidney ADRs is due to changes in kidney blood flow.
Prostaglandins normally dilate the afferent arterioles of the glomeruli. This helps
maintain normal glomerular perfusion and glomerular filtration rate (GFR), an
indicator of kidney function. This is particularly important in kidney failure where
the kidney is trying to maintain renal perfusion pressure by elevated angiotensin II
levels. At these elevated levels, angiotensin II also constricts the afferent arteriole
into the glomerulus in addition to the efferent arteriole it normally constricts.
Since NSAIDs block this prostaglandin-mediated effect of afferent arteriole
dilation, particularly in kidney failure, NSAIDs cause unopposed constriction of the
afferent arteriole and decreased RPF (renal perfusion flow) and GFR.
There are 2 types of cyclooxygenases, COX1 and COX2. COX1 is inherently and
continuously produced by the body while COX2 is produced only during tissue
injury at the site of damage.
Some drugs inhibit both cyclooxygenases while some selectively inhibit COX2.
The 2 types of cyclooxygenase inhibition:
Non – selective COX inhibitors – These NSAIDs block both the cyclooxygenase 1
and 2 pathways resulting in two effects – arresting inflammation and preventing
platelet aggregation.
Selective COX2 inhibitors – This class of NSAIDs were developed mainly to inhibit
inflammation without the side effects that arise from inhibition of COX-1 which
include gastric and duodenal ulcers and bleeding. As such, these drugs can be
used to treat inflammatory disorders but are not useful for the prevention of
diseases that depend on COX-1 inhibition. Desirable effects of NSAIDs.
Classification
Salicylates
Diflunisal (Dolobid)
Salsalate (Disalcid)
Ibuprofen
Dexibuprofen
Naproxen
Fenoprofen
Ketoprofen
Dexketoprofen
Flurbiprofen
Oxaprozin
Loxoprofen
Pelubiprofen
Zaltoprofen
Indomethacin
Tolmetin
Sulindac
Etodolac
Ketorolac
Diclofenac
Aceclofenac
Bromfenac
Nabumetone (drug itself is non-acidic but the active, principal metabolite has a
carboxylic acid group)
Piroxicam
Meloxicam
Tenoxicam
Droxicam
Lornoxicam
Isoxicam
Phenylbutazone (Bute)
Mefenamic acid
Meclofenamic acid
Flufenamic acid
Tolfenamic acid
INDICATIONS
NSAIDs are often suggested for the treatment of acute or chronic conditions
where pain and inflammation are present. NSAIDs are generally used for the
symptomatic relief of the following conditions
Rheumatoid arthritis
Osteoarthritis
Localized musculoskeletal syndromes like sprains, strains, and low back pains
Gouty arthritis
Psoriatic arthritis
Dysmenorrhea
Pyrexia (fever)
Renal colic
Macular edema
Traumatic injury
Cerebrovascular disease
Angina
Colon cancer
Headaches
Dizziness
Abdominal pain
Dyspepsia
Nausea
Vomiting
Rashes
Pruritus
Asthma attack
Thrombocytopenia
Neutropenia
Aplastic anemia
Liver failure
Renal insufficiency
Renal failure
Hyperkalemia
Proteinuria
Myocardial infarction
Gastrointestinal bleeding
Patients who have recently undergone coronary artery bypass graft surgery
– studies have shown an increased risk of myocardial infarction for some
NSAIDs for these patients.
NSAIDs should be used with caution in patients with the following conditions:
Medication allergy
Hypertension
Diabetes mellitus
Bronchial asthma
Concurrent condition that has bleeding tendencies like dengue and chikungunya
fevers
Recent viral infections like chickenpox and flu. Studies have associated NSAID use
with the development of Reye syndrome, a condition that causes swelling in the
liver and brain.
Drug Interactions with NSAIDs
NSAID metabolism is mainly through the liver by way of the cytochrome P450
system and eliminated through the kidneys. Therefore, all drugs that are
metabolized by these similar enzymes and pathways will have interactions with
NSAIDs to varying extents.
Drugs that act on the hematopoietic system such as anti-thrombotic and other
anti-platelets increase the risk of bleeding. Examples of these drugs are warfarin,
heparin, novel anti-coagulants, and other anti-platelets.
NSAIDs attenuate the effect of most anti-hypertensive drugs. Taking NSAIDs with
these drugs may decrease their effectiveness and cause increased blood pressure.
Such drugs include ace-inhibitors, angiotensin receptor blockers, thiazide diuretics
and loop diuretics.
NSAIDs may affect the kidney through the regulation of the renal artery’s blood
flow. Drugs that act on the kidneys may precipitate damage when used with
NSAIDs. Drugs that are eliminated through the kidneys may show decreased renal
clearance and increased toxicity. These drugs include the mood disorder drugs,
anti-cancer drugs, cardiac drugs, and nephrotoxic anti-bacterial drugs like
aminoglycosides.
Some drugs interact with NSAIDs through their metabolism in the liver. Anti-
epileptic drugs may show decreased hepatic clearance and displacement from
protein binding since NSAIDs are also highly protein-bound.
Oral anti-diabetic drugs may induce further hypoglycemia when taken with
NSAIDs
Drugs that affect the gastrointestinal tract like corticosteroids may increase the
risk of ulceration and bleeding. Antacids may interfere with the absorption of
NSAIDs.
Risk for Impaired Urinary Elimination related to the effects of NSAIDs on the
kidneys
1. Verify the patient’s diagnosis and the need for administering NSAIDs. To
confirm the indication for administering NSAIDs.
2. Check the patient’s allergy status. Previous allergic reaction to NSAIDs may
render the patient unable to take them. Alternatives to NSAIDs should therefore
be considered in case of allergy.
6. Check the patient’s serum blood sugar levels if taking anti-diabetics alongside
NSAIDs. Patients on NSAIDs and oral anti-diabetics may experience hypoglycemic
episodes.
7. Ask the patient for any medical or family history of hemophilia, gastrointestinal
ulcers, or bleeding disorders. NSAIDs have anti-platelet effects that can
exacerbate the bleeding tendencies and may be fatal for these patients.
9. NSAIDs are best taken on full stomach to reduce the occurrence of stomach
upset.
10. NSAIDs should always be taken on time to prevent any delays and errors
during treatment.
11. Educate the patient about the action, indication, common side effects, and
adverse reactions to note when taking NSAIDs. Instruct the patient on how to self-
administer oral NSAIDs. Monitor the patient’s input and output. NSAIDs may
cause impaired urinary elimination.
VASOPRIN
DOSAGE: For cardio vascular treatment 1-2 tablet daily, for pain 4-8 tablet of
75mg every 4hours daily.
Contraindication: as above.
Indications: as above
Dosage: one or two tablet b.d or 1’2-1.8g initially for adult daily. For juvenile
rheumatoid arthritis 30-40mg per kg bodyweight in 3-4 divided doses. For fever
and pain in children 20-30mg daily in divided doses.1-3yrs 100mg tds daily,4-6yrs
150mg tds daily,7-9yrs 200mg tds and 10-12yrs 300mg tds daily.
Contraindication: as above
PIROXICAM (FELDENE)
MELOXICAM
Dosage: for osteoarthritis 7.5-15mg daily. For rheumatoid arthritis and ankylosing
spondylitis 15mg once daily for elderly people 7.5mg daily.
MEFENEMIC ACID
Dosage: adult and children over 14 yrs 75-150mg in 2-3 divided doses daily. For
primary dysmenorrhea 50mg-150mg daily
Contraindication: As above
ACECLOFENAC
PARACETAMOL (Acetaminophen)
Mode of action: act on the heat regulation center in the hypothalamus to send a
sympathetic impulse to the body of the sweat gland under to the skin to produce
more sweat evaporates and producing cooling effect and lowering the body
temperature.
Nursing responsibility:
Patient should not exceed maximum recommended dose of 4grm (8 tablets) daily.