Mosby's 2014 Nursing Drug Reference (254 page)

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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

medroxyPROGESTERone (Rx)

(me-drox′ee-proe-jess′te-rone)

Depo-Provera, Depo-sub Q Provera, Gen-Medroxy
, Provera

Func. class.:
Antineoplastic, hormone, contraceptive

Chem. class.:
Progesterone derivative

Do not confuse:
medroxyPROGESTERone
/methylPREDNISolone
Provera
/Premarin/Covera

ACTION:

Inhibits secretion of pituitary gonadotropins, which prevents follicular maturation and ovulation; antineoplastic action against endometrial cancer

USES:

Uterine bleeding (abnormal); secondary amenorrhea; prevention of endometrial changes associated with estrogen replacement therapy (ERT); contraceptive; inoperable, recurrent, metastatic endometrial/ renal cancer

Unlabeled uses:
Hot flashes; symptoms of menopause; paraphilia (men); hot flashes (men) with prostate cancer

CONTRAINDICATIONS:

Pregnancy (X), hypersensitivity, reproductive cancer, genital bleeding (abnormal, undiagnosed), missed abortion, stroke, cerebrovascular disease, cervical cancer, hepatic disease, uterine/vaginal cancer

 

Black Box Warning:

Breast cancer, MI, stroke, thromboembolic disease, thrombophlebitis

Precautions:
Breastfeeding, hypertension, asthma, blood dyscrasias, gallbladder disease, CHF, diabetes mellitus, bone disease, depression, migraine headache, seizure disorders, renal/hepatic disease, family history of cancer of breast or reproductive tract, bone mineral density loss, ocular disorders, AIDS/HIV, alcoholism, children, hyperlipidemia

 

Black Box Warning:

Cardiac disease, dementia, osteoporosis

DOSAGE AND ROUTES
Calculator
Secondary amenorrhea

• Adult:
PO
5-10 mg/day × 5-10 days

Uterine bleeding

• Adult:
PO
5-10 mg/day × 5-10 days starting on 16th or 21st day of menstrual cycle

With ERT

• Adult:
PO
5-10 mg daily × 10-14 or more days/mo (sequential estrogen); 2.5-5 mg daily (continuous estrogen)

Contraceptive

• Adult:
IM
(contraceptive inj) 150 mg q12wk;
SUBCUT
(depot SUBCUT Provera 104 inj) 104 mg q3mo

Endometrial/renal cancer

• Adult:
IM
400 mg-1 g (using 400 mg/ml depot inj susp) weekly

Hot flashes/symptoms of menopause (unlabeled)

• Adult (female):
PO
20 mg/day;
IM
150 mg monthly

Hot flashes (men) in prostate cancer (unlabeled)

• Adult (male):
IM
Depot 150 or 400 mg

Available forms:
Tabs 2.5, 5, 10 mg; inj susp, 150, 400 mg/ml; depot-SUBCUT inj: 104 mg/0.65 ml

Administer:
PO route

• 
Give without regard to food

IM route

• 
Visually inspect particulate matter and discoloration before use

Depo-provera contraceptive injection suspension

• 
IM only,
never
IV

• 
Instruct patient on risks and warnings associated with hormonal contraceptives (see Patient Information)

• 
The possibility of pregnancy should be excluded before giving the first dose of medroxyprogesterone or whenever more than 14 wk has passed since the last dose

• 
Do not dilute

• 
Shake vigorously immediately before administration

• 
Inject deeply into the gluteal or deltoid muscle; Aspirate before injection to avoid injection into a blood vessel

Depo-provera sterile aqueous suspension, preserved

• 
IM only,
never
IV

• 
Instruct patient on risks and warnings associated with progestin use (see Patient Information)

• 
Shake vigorously immediately before use

• 
When multidose vials are used, take special care to prevent contamination

• 
Inject deeply into the gluteal or deltoid muscle; aspirate before injection

SUBCUT route

depo-subq provera 104 contraceptive injection suspension
only

• 
For subcut only,
never
give IM or IV

• 
Instruct patient on risks and warnings associated with hormonal contraceptives (see Patient Information)

• 
Shake vigorously for at least 1 min before use

• 
Inject the entire contents of the prefilled syringe subcut into the anterior thigh or abdomen, avoiding bony areas and the umbilicus; gently grasp and squeeze a large area of skin in the chosen injection area, ensuring that the skin is pulled away from the body; insert the needle at a 45-degree angle; inject until the syringe is empty; this usually requires 5-7 sec; following use, press lightly on the injection site with a clean cotton pad for a few seconds; do not rub the area

SIDE EFFECTS

CNS:
Dizziness, headache, migraines, depression, fatigue, nervousness

CV:
Hypotension, thrombophlebitis, edema,
thromboembolism, stroke, PE, MI

EENT:
Diplopia

GI:
Nausea
, vomiting, anorexia, cramps, increased weight,
cholestatic jaundice,
abdominal pain

GU:
Amenorrhea, cervical erosion, breakthrough bleeding, dysmenorrhea, vaginal candidiasis, breast changes,
gynecomastia, testicular atrophy, impotence
, endometriosis,
spontaneous abortion,
vaginitis, libido increased/decreased

INTEG:
Rash, urticaria, acne, hirsutism, alopecia, oily skin, seborrhea, purpura, melasma, photosensitivity, injection site reaction

META:
Hyperglycemia

MS:
Decreased bone density

SYST:
Angioedema, anaphylaxis

PHARMACOKINETICS

PO:
Duration 24 hr; excreted in urine and feces; metabolized in liver

INTERACTIONS

Decrease:
medroxyPROGESTERone action—aminoglutethimide, carBAMazepine, phenytoins, PHENobarbital, rifampin

Decrease:
bone mineral density—anticoagulants, corticosteroids

Drug/Lab Test

Increase:
LFTs, HDL, triglycerides

Decrease:
GTT, HDL

NURSING CONSIDERATIONS
Assess:

• 
Pelvic exam, Pap smear before treatment, periodically

 
Severe allergic reaction, angioedema;
have EPINEPHrine and rescusitative equipment available

• 
Weight daily; notify prescriber of weekly weight gain >5 lb; bone mineral density

• 
B/P at beginning of treatment and periodically

• 
I&O ratio; be alert for decreasing urinary output, increasing edema

• 
Hepatic studies: ALT, AST, bilirubin periodically during long-term therapy

• 
Edema, hypertension, cardiac symptoms, jaundice

• 
Mental status: affect, mood, behavioral changes, depression

 

Black Box Warning:

This product should not be given to those with breast cancer, MI, stroke, thromboembolic disorders

• 
Bone mineral density loss:
in those taking anticoagulants, corticosteroids with Depo-Provera or Depo-sub Q Provera

 

Black Box Warning:

Use of product shown to increase dementia in women ≥65 yr old; use may increase osteoporosis in long-term treatment; those who smoke also at greater risk; adequate calcium and vit D should be taken

Perform/provide:

• 
Storage in dark area

Evaluate:

• 
Therapeutic response: decreased abnormal uterine bleeding, absence of amenorrhea

Teach patient/family:

• 
To avoid sunlight or to use sunscreen; photosensitivity can occur

 
To report breast lumps, vaginal bleeding, edema, jaundice, dark urine, clay-colored stools, dyspnea, headache, blurred vision, abdominal pain, sudden change in speech/coordination, numbness or stiffness in legs, chest pain; males to report impotence, gynecomastia

• 
To report suspected pregnancy (X); fertility returns 6-12 mo after discontinuing

 

Black Box Warning:

Long-term use decreases bone density; exercise, calcium supplements can help lessen osteoporosis

BOOK: Mosby's 2014 Nursing Drug Reference
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