Exam (elaborations) NR PHARMACOLOGY INTRODUCTION TO PHARMACOTHERAPEUTICS
NR PHARMACOLOGY
INTRODUCTION TO
PHARMACOTHERAPEUTI
CS
INTRO TO PHARMACOTHERAPEUTICS
Prescription Writing Need at least 2 patient identifiers: Name, DOB, Address, Date of Rx, Prescriber name, address, license number, DEA number if applicable, Info for supervising MD,
Drug: name/strength/dose/route/QTY/refills, Signature
JC ¡§Do Not Use¡¨ List
¡E U: write out ¡§unit¡¨
¡E IU: write out ¡§international units¡¨
¡E Q.D., Q.O.D.: write out daily or every other day
¡E Trailing/leading zeros
¡E MS, MSO4, MgSO4: write morphine sulfate or magnesium sulfate
¡E £gg: write mcg
¡E H.S.: write half-strength or at bedtime
¡E T.I.W.: write three times weekly or 3 times weekly
¡E S.C. or S.Q.: write Sub-Q or subQ or subcutaneously
¡E D/C: write discharge
¡E c.c.: write mL
¡E AS, AD, AU, OS, OD, OU: write out, e.g., both eyes or left ear
ANTIBIOTICS
Class Drug MOA Uses/Coverage ADR/DDI Education/Other
PCN:
1st Gen
Pen G (IV)
Inhibit cell wall
synthesis, Bactericidal
Pneumococcal pneumonia
Benzathine penicillin (IM) Syphilis, strep throat
Pen VK (PO) Gram + coverage and Treponema pallidum
PCN:
2nd Gen
Nafcillin (IM/IV)
Antistaphylococcal, Cloxacillin (PO) MSSA
Dicloxacillin (PO)
PCN:
3rd Gen
Ampicillin (PO) Extended-spectrum: G(+) PLUS some G(-);
Amoxicillin (PO) OM, URI
Augmentin
(amox + clavulanate)
Diarrhea, Good for beta-lactamase: H.Flu,
M.Cat
PCN:
4th Gen
Zosyn (piperacillin +
tazobactam) (IV)
Broad spectrum, covers Pseudomonas, many
G(-)
Cephalosporin:
1st Gen
Cefazolin (IM, IV)
Inhibit cell wall
synthesis
good Gram + coverage, NO MRSA coverage
Cross-sensitivity with PCNs
Cephalexin (PO)
Cephalosporins:
2nd Gen
Cefaclor Not as good G+ but some G(-); OM, Strep
Cefuroxime (IM, IV, PO) pharyngitis
Cephalosporins:
3rd Gen
Ceftriaxone (IM, IV)
better G- but lower G+ coverage, High risk w/
some for ESBL resistance
Ceftriaxone good for
gonorrhea d/t single dose
Cefotaxime (IM, IV)
Cefixime (PO)
Cephalosporins:
4th Gen Cefepime (IM/IV) Good G+ and G- coverage, Covers
Pseudomonas
Cephalosporins:
5th Gen Ceftaroline (IV) G- as 3rd-gen plus MRSA coverage
Carbapenems
Doripenem
Inhibit cell wall
synthesis
Broader than other BL-abx
All IV, IM, saved for very broad coverage
May have cross-sensitivity
to PCNs
Ertapenem Ertapenem: not good
Pseudomonas coverage
Imipenem & cilastatin
Meropenem
Monobactam Aztreonam: IM, IV, inhale Inhibit cell wall G- ONLY, Covers Pseudomonas Never use for empiric tx,
1
synthesis Good for PCN-allergic
Vancomycin IV
Inhibit cell wall
synthesis
Mainly for G+ and MRSA IV ADR: dose-related
ototoxicity &
nephrotoxicity; Red man
(infusion NOT allergy)
Dose for renal fxn, monitor
serum levels
Vancomycin PO For C. diff. colitis
Telavancin Inhibit cell wall
synthesis
Alternative to vancomycin
Covers G+ and MRSA
ADR: Teratogenic and QT
prolongation No drug monitoring
Macrolides
Erythromycin
Inhibit protein
synthesis, bind to 50s
ribosomal subunit
G+, G-, and atypicals, Often used to treat G+
in pen-allergic patients;
Enzyme inhibitor: E C A
Must watch with: CBZ, warfarin, statins, etc.
Allergic reactions are rare!
Clarithromycin ADR: n/v, metallic taste Improved H.Flu vs. E-mycin
Azithromycin Long 1/2 life, good for
Chlamydia, other atypicals
Tetracyclines
Doxycycline Inhibit protein
synthesis, bind to 30s
ribosomal subunit
Coverage very broad: G+, G-,aerobic and
anaerobic, spirochetes, mycoplasmas,
rickettsiae, chlamydiae, some protozoa, MRSA
PO
High levels of resistance
CI: Avoid with chelating agents (MVI, antacid, milk, iron),
Avoid in pregnancy and small children (8) ¡V Binds Ca and
will stain teeth
ADR: n/v, liver Minocycline disease, phototoxicity
Tigecycline IV Derivative of
minocycline
MRSA, MDRSp, VRE, ESBL-producing G-,
many anaerobes, NOT for Pseudomonas; for
Complicated SSTIs, intraabdominal ifxn, CAP
Aminoglycoside
Amikacin Inhibit protein
synthesis, bind to 30s
ribosomal subunit
G- including Pseudomonas Monitor renal function and serum drug levels!
Gentamicin ADR: ototoxicity, nephrotoxicity
Tobramycin
Clindamycin
Inhibit protein
synthesis, bind to 50s
ribosomal subunit
Mainly for anaerobic coverage
PO or IV and in some topicals, MRSA PO ADR: rashes and high rate of C.diff.
Linezolid (Zyvox)
Inhibit protein
synthesis, bind to 50s
ribosomal subunit
PO & IV
Use for resistant organisms: MRSA, VRSA,
VRE, penicillin-resistant Strep. pneumo
Caution for Serotonin
Syndrome Might offer benefit when
transitioning to outpatient
Fluoroquinolones
Ciprofloxacin
Inhibit nucleic acid
synthesis ¡V inhibit
topoisomerase
UTI, GI, Pseudomonas
broad G-,
respiratory FQs
with improved G+
coverage
ADR: C.diff colitis!! CNS: seizure, dizziness; Cardiac: QT
prolong; MS: tendon, cartilage; Endo: glycemic control;
Skin: photosensitivity, rash
DDI: antacids, Fe, Ca, Zn
Levofloxacin UTI, GI, LRI, URI, skin
Moxifloxacin LRI, URI, GI, skin (no
UTI!!)
Others PO, otic, ophthalmic
Folate Antagonist TMP-SMX
(Bactrim, Septra)
Broad with G+ and G-, NO Pseudomonas
Common for UTI, MRSA PO
ADRs: rash (simple to SJS),
photosensitivity, crystalluria
(need to counsel)
Dose based on TMP (more
important in PO liquid)
Miscellaneous
Metronidazole
Covers protozoa, anaerobes
**DOC: C.diff. colitis
Trichomoniasis; Various infections of: skin,
bone, CNS, GYN, GI, LRI, endocarditis
ADR: Avoid with EtOH. Metallic taste
Nitrofurantoin unclear, thought to
inhibit several enzyme
pathways and possibly
Use in simple UTI treatment and prophylaxis
NOT pyelonephritis or complicated cystitis
CI: ClCr 60 mL/min; Do not use in renal impairment
Warnings/Caution: Hepatic disease, Elderly
2
cell wall synthesis
3
PHARM FALL 2013 BLOCK I: DERM & EENT
INTRODUCTION TO DERMATOLOGIC PRODUCTS
Determinant of
Pharmacologic
Response
1. Permeability and penetration ¡V hydrated dehydrated, thin thick, trauma no trauma
2. Concentration gradient ¡V greater concentration „³ greater amount per unit time (threshold may exist)
3. Dosing ¡V time left on skin, frequency, quantity; dermis acts as barrier and can effect duration
4. Vehicle ¡V cream, ointment, liquid, solution
5. Occlusion ¡V maximizes efficacy, increases absorption, protection
Drug Delivery
Systems
„h Emulsions ¡V drug particle contained w/in vehicle/base; Indication for different types of products (dry/wet, sensitivity/pain, size, location, acute/chronic)
„h Creams ¡V most common vehicle, no occlusion
„h Ointments ¡V common, good for dry lesions due to occlusive properties; NOT for intertriginous areas; can be cosmetically unpleasing
„h Gels ¡V clear, non-greasy, non-staining, non-occlusive, quick drying; can sting on application and be drying (due to EtOH)
„h Solutions ¡V evaporate quickly (drying), used in acute/weeping/oozing wounds
o Tinctures ¡V alcohol-based solution, used for extreme drying properties
„h Aerosols ¡V advantage for painful skin, but expensive and not efficient dosage form
„h Lotions ¡V good for tender areas, spreads easily, evaporates quickly, good for large areas
„h Powders ¡V used to absorb moisture/friction; caution w/ very wet lesions due to crusting
Choosing
Which Drug
Delivery System
to Use
DRY wet lesions and WET dry lesions **more liquid agents dry better
„h Acute inflammation (oozing/weeping/vesication/edema/pruritis) „³ aqueous vehicles, powders, lotions, sprays, aerosols
„h Subacute inflammation (crusting/oozing/pruritis) „³ creams, gels
„h Chronic inflammation (lichenification/dryness/erythema/pruritis/scaling) „³ ointments
ANDROGENIC ALOPECIA Tx goal: reduce loss and maintain existing hair **If you stop therapy, hair loss WILL return!
Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Minoxidil
Changes follicle size & growth cycle of
hair to „^ f hair & thicker/longer shaft
Topical formulation only to limit and
contain ADR („`BP); OTC, 1st line M & F
ADR: local irritation, undesirable
growth if inappropriately use **welltolerated
Wash hands after application,
treatment must be continuous
Finasteride Type II 5-alpha-reductase inhibitor, PO (tablet) formation that only grows *CI: pregnancy Caution in women of child-bearing
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Vehicles for Topically Applied Drugs
Cream Ointment Gel/Foam Lotion/Solution/Foam
Pharmacological
Advantage
Leaves concentrated drug at skin
surface Protective oil film on skin Concentrates drug at surface after
evaporation
Advantages for
Patient
Spreads and removes easily,
no greasy feel
Spreads easily, slows water evaporation,
gives cooling effect
Non-staining, grease-less, clear
appearance Low residue on scalp
Locations on Body Most locations Avoid intertriginous areas* Foams well for scalp and other
hairy locations
Solutions and foams are well
accepted on scalp
Disadvantages Needs preservatives Greasy to very greasy, stains clothes Needs preservatives, high alcohol
can be drying
Occlusion Low Moderate to high, increases skin
moisture
inhibits conversion of testosterone to
dihydrotestosterone (reverse loss)
hair at vertex/frontal scalp; first line
for men, second line for women
ADR: „`libido, erectile dysfunction,
ejaculation disorder, „`ejaculation vol
age, wash hands/gloves, treatment
must be continuous
SYSTEMIC ANTIFUNGALS
Class Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Amphotericin B
(¡§Amphoterrible¡¨)
binds to ergosterol and
alters permeability; large
spectrum of activity
IV; only used in infectious disease with high
resistance *lipid formations are less toxic, but still
not good
ADRs: EXTREMELY TOXIC
(nephrotoxicity, infusionrelated
toxicity)
Azoles
Fluconazole
(Diflucan)
inhibit synthesis of
ergosterol by blocking
demethylation of lanosterol
IV and PO; Important treatment for infections due
to Candida; drug of choice for vaginal yeast
infections
Itraconazole
IV and PO *bioavailability varies, PO solution
achieves higher serum concentrations; Used for
fungal nail infections
Can cause liver problems ¡V must
get liver enzymes checked every 4-
6 weeks
Voriconazole IV and PO; Broad spectrum triazole used for
serious infections, first line for aspergillosis
ADR: visual abnormality
Posaconazol
e
PO suspension
Broad-spectrum triazole, but can cause many DDIs
*Enhanced w/ high-fat meal,
splitting dose in fasting
Echinocandins
disrupts cell wall structure
formation by inhibiting £]-
glucan synthase
IV only; used to treat significant fungal infection ¡V
integral component of Aspergillus and Candida cell
wall
Generally well tolerated
(but expensive)
*more common/better
tolerated/less DDIs than azole
Flucytosine
disrupts cell wall formation
via pyrimidine analog
PO only, rarely used as monotherapy due to rapid
resistance development
Spectrum: Cryptococcus spp, Candida spp; used to
treat cryptococcal meningitis in combination w/
AmB
Key Points of Systemic Antifungals
„h Always consider hepatic function (liver disease, heavy EtOH use, etc.)
„h Review patient¡¦s medical history to avoid DDIs
„h Systemic ¡Vazole agents in primary care are mainly used for skin/nail disorders, vaginal yeast infections (fluconazole)
TOPICAL ANTIFUNGALS
Class Drug MOA Indication Specific Education/Other
Topical
Azoles
Block biosynthesis of ergosterol Tinea pedis/cruris/corporis, tinea versicolor,
cutaneous candidiasis, vaginal candidiasis
*Most effective topical antifungal for
treatment of dermatophytes
Topical
Allylamines,
Butylamine
Naftifine inhibit squalene epoxidase (key enzyme in
ergosterol biosynthesis pathway)
Tinea pedis/cruris/corporis, tinea versicolor
Terbinafine
(Lamisil)
**Terbinafine = tx for nail fungus
Butenafine
Topical
Polyene Nystatin Bind to ergosterol in fungal cell membrane,
changes membrane permeability
cutaneous infections caused by Candida
albicans, other Candida spp
*not useful against dermatophytes
*highly toxic systemically
Other Selenium exerts a cytostatic effect of cell of epidermis tinea versicolor Lotion, Shampoo formulations OTC (well-
5
Sulfide and follicular epithelium tolerated)
Tolnaftate Distorts the hyphae and stunts mycelial
growth of fungal species
Tinea pedis/cruris/corporis, tinea versicolor (Tinactin) *tough-actin tinactin; Cream,
solution, powder, spray, gel forumations OTC
Ciclopirox
alters integrity of fungal cell membrane skin, superficial nail infections; tinea
pedis/cruris/corporis, tinea versicolor *activity
against Candida
Cream, lotion, nail laquer (Penlac)
formulations
Systemic Agents for Superficial Infections
*Fluconazole Itraconazole Ketoconazole Terbinafine Griseofulvin
Indicated for candidiasis
*yeast/vaginal infections
Single dose is used for treatment
Indicated for candidiasis,
dermatophytes (tineas),
onychomycosis (nail fungus)
Multiple DDIs ¡V Inhibited CYP3A4
Indicated for candidiasis,
dermatophytes
Multiple DDIs, potential
hepatotoxicity *only last line in
life-threatening infection
PO and topical available
Indicated for candidiasis,
dermatophytes, onychomycosis
Potential hepatotoxicity ¡V
monitor liver enzymes
Inhibits mitosis, rarely used
Indicated for dermatophytes and
onychomycosis
*Pulse Therapy (Terbinafine and Itraconazole): Used in onychomycosis treatment, has some evidence for less toxicity (dosed daily 1 week, off 3 weeks) to decrease ADRs, DDIs
DRUG ERUPTIONS
Types of Drug Eruptions „h Mild rash, itching, dry skin „³ severe, potentially life-threatening conditions)
„h SJS, TEN, Angioedema, Vasculitis, Coagulent-induced skin necrosis
General Approach to
Drug Reactions
(1) Recognize that problem may be drug-related Identify agent (2) STOP OFFENDING AGENT (3) Determine severity (i.e. triage situation) (4) Treat
sequelae **Don¡¦t forget to EDUCATE PATIENT
Reaction Characteristics Common Offenders
Acneiform Reactions Differ from true acne: no comedone, uniform appearance of lesions, location,
age, recent drug exposure
glucocorticoids, oral contraceptives, lithium, anabolic steroid
Photosensitivity
Reactions
Phototoxic reactions ¡V exaggerated sunburn or increased sensitivity to light;
UVA causes alteration of drug to toxic form (common)
Photoallergic reactions ¡V manifests in bullae, urticaria, sunburn; UVA alters
drug to antigen and leads to allergic response (common)
antibiotics, antidepressants, hypoglycemics, oral contraceptives,
antipsychotics, antihypertensives
Allergic Contact
Dermatitis
Topical administration can cause localized allergic response, reaction
widespread if given systemic drug after topical sensitization
neomycin (Neosporin), benzocaine, diphenhydramine (Benadryl)
Erythema Multiforme Lesions of various forms including Target lesions; affect mucous membranes allopurinol, barbiturates, phenothiazine, sulfonamides
Stevens-Johnson
Syndrome (SJS)
Most common severe eruption; can be life-threatening (est. 5-20%) sulfonamides*, FQs, allopurinol, carbamazepine, pregnancy,
infection, radiation, cancer, foods
Topical Epidermal
Necrosis (TEN)
Prodrome of milder symptoms (fever, fatigue, arthralgias, sore throat); can be
fatal (est. 30%)
allopurinol, aminopenicillins, carbamazepine, sulfonamides*,
infection, foods
Erythema Nodosum Erythematous rash with tender nodules commonly on legs (usually no
mucosal involvement)
oral contraceptives*, analgesics, sulfonamides
Drug Hypersensitivity
Reaction
Multiple names/varied constellation of symptoms and signs may lead to
misdiagnosis; Typically start w/ fever, widespread maculopapular rash on
trunk, arms, legs; organ damage may follow, fatal in 10%
sulfonamides, PCNs, anticonvulsants, antimalarials
Fixed Drug Eruption Erythematous lesions of various types (nodules, bullae) common on genitals,
face *always in same spot
Caused exclusively by drugs (antibiotics, anti-inflammatories,
oral contraceptives) *generally resolve after offending drug d/c
Maculopapular Typical rash, #1 drug reaction manifested in skin *classic PCN rash ampicillin, amoxicillin, allopurinol
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Eruptions
Scarlatiniform (scarlet fever-like, erythematous, wide-spread lesions) or
Morbiliform (measles-like, reddish/brown macules coalesce)
Usually 1w after drug exposure, resolve w/in 2 weeks after d/c
Urticaria (Hives)
Immediate, IgE-mediated (hypersensitivity) reactions
Lesions will usually migrate until offending allergen ins topped *can be
isolated or widespread ***Patients w/ urticaria are at increased risk for
anaphylaxis with future exposure (do NOT re-challenge)
aspirin (ASA), penicillins
Angioneurotic Edema
(Angioedema)
Severe form of urticaries (hives penetrate deeper); involve lips, tongue, eyelids
(fatal if tongue, throat, larynx); May take weeks ¡V years, can happen at any
time
***ACEIs (angiotensin-converting enzyme inhibitors); patients
must be warned to watch swelling
TOPICAL ANTIBIOTICS (tx mild skin infections)
Drug Indication ADRs/DDI/CI
Bactracin (OTC) Broad G+ coverage, not for MRSA, used in combination products Topical application only due to severe nephrotoxicity with systemic use
Neomycin (OTC) Common, broad-spectrum used for minor infections (abrasions, cuts, etc.),
not for MRSA
increased risk for hypersensitivity if in combination with other antibiotics
Mupirocin (Rx) DOC for impetigo (superficial), used for multiple G+ skin infections, MRSA
nasal colonization
Retapamulin Topical agent used for impetigo only
Silver
Sulfadiazine
Used in treatment/prevention of burns *caution w/ sulfa allergy
SELECT VIRAL SKIN DISORDERS
Condition Management
General Concepts „h Antivirals have potential for DDIs „³ complete a thorough medication history before prescribing *adjustment for renal/hepatic disease
„h Must also use supportive therapy/treat complications (fever, arthralgias, pain, post-herpetic neuralgia)
Oral-Facial Herpes
(Herpes Labialis)
Most are self-limiting (10 days) and treat with respect to immune status and if prolonged disease is likely
Topical *should begin w/in 1 hour of first signs/symptoms **all must be
frequently applied (disadvantage)
„h Acyclovir (Zovirax) cream ¡V Rx only
„h Docosanol (Abreva) cream ¡V OTC
„h Penciclovir (Denavir) cream ¡V Rx only
Oral *can be good option for immunosuppressed **easier to take, but
costly (weigh costs/benefits)
„h Acyclovir (Zovirax)
„h Famciclovir (Famvir) ¡V single dose
„h Valacyclovir (Valtrex)
Varicella-Zoster
Infection
Varicella (Chickenpox)
„h Childhood vaccine available
„h Acyclovir ¡V PO
Herpes Zoster (Shingles)
„h Adult vaccine available
„h Acyclovir, Famciclovir (fewer doses), Valacyclovir (fewer doses
Genital Herpes Acyclovir, Famciclovir (fewer doses), Valacyclovir (fewer doses)
Warts
Vaccine available
Treat w/ cryotherapy, instrumentation (cutting or curettage)
Imiquimoid (Aldara) cream or Podofilox (Condylox) gel for genital warts
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CORTICOSTEROIDS
General
Concepts
„h Glucocorticoids ¡V receptors widespread throughout body (cortisol)
„h Mineralocorticoids ¡V receptors in kidney, colon, salivary/sweat glands, brain (aldosterone)
o Regulates water volume and concentration of electrolytes ¡V acts on kidney tubules, collecting ducts, enhances Na+ reabsorption
o Used less frequently than glucocorticoids
Class MOA Indications/Management ADR/Patient Education
Systemic
Glucocorticoids
„h Anti-Inflammatory
„h Promotion of
Metabolism (**DM
patients sugar will
increase)
„h Increased
Resistance to Stress
„h Alteration of Blood
Cell Levels in Plasma
Acute Adrenal Insufficiency
„h Dx: ACTH stimulation test; Tx: IV hydrocortisone + glucose
Chronic (Addisons) Adrenal Insufficiency:
„h Tx: PO hydrocortisone daily, prednisone or dexamethasone
„h Some patients normalized by hydrocortisone + salt intake, many require
mineralcorticoid replacement
„h Fludrocortisone** mineral action
Inflammatory/Autoimmune Disease: Provide sx relief only ¡V do not cure!!
„h High initial dose and taper over days to allow adrenal recovery
„h Tablets (#1), can also be injected to minimize systemic effects
Asthma
„h Inhaler administration daily *minimizes systemic effects, ADRs
„h Agents: Triamcinolone, Beclomethasone, Flunisolide, Fluticasone
„h PO for severe exacerbations * chronic bronchitis and emphysema
Allergic Disease
„h Relief delayed 12-24h, appropriate for severe/long /systemic reactions
„h PO or IV, nasal spray steroids are first choice treatment for allergic rhinitis
Other:
„h Infectious Disease: supplemented, not 1st line
„h Blood Malignancies
„h Traumatic Injury/Organ Transplantation: Spinal cord injury (NOT effective w/
head injury), Organ transplantation
„h Preterm labor
„h Chemotherapy
ADRs of Corticosteroids
„h Fluid/electrolyte imbalances
„h Metabolic: hyperglycemia/glucosuria
(close management w/ diet, insulin)
„h Immune suppression: Increased
susceptibility to infection with chronic use
„h GI acid production: increased risk of peptic
ulcer, (esp. in conjunction w/ NSAIDs)
„h Myopathy: muscle wasting, takes high
dose
„h Osteoporosis, Osteonecrosis
„h Cataracts
„h Behavioral changes ¡V ¡§steroid psychosis¡¨
„h Growth suppression in children ¡V
especially systemic steroids **use of
steroids in chronic asthma in children is a
common concern
„h Cushing¡¦s Syndrome ¡V chronic use; upper
body obesity, rounded/moon face, thin
arms/legs
Withdrawal from Glucocorticoids: Sudden
withdrawal can be life-threatening (acute
adrenal insufficiency) **taper off if used
2weeks!!
Topical
Corticosteroids
Inflammatory skin diseases
„h 1% hydrocortisone ointment +/- occlusive dressing, minimal systemic
absorption
„h Systemic administration for widespread/severe exacerbations (prednisone,
prednisolone)
„h Many preparations ¡V betamethasone (most potent), triamcinolone,
clobetasol
„h Fluorinated steroids should NOT be used on face (dexamethasone,
triamcinolone, betamethasone, ¡§flu-sone,lone,rone)
* DOC for skin inflammation and pruritus but avoid use in infectious etiologies
(except when combined w/ antifungal)
Ocular Inflammation
„h Dexamethasone eye drops or ointment **should always be used under
Aoid overuse, use lowest potency *educate
patient not to exceed recommended dosing
Don¡¦t forget systemic effects: children, elderly,
liver disease, thin skin, use of occlusion/high
potency agents (ointments)
ADRs *fewer than systemic
Local ¡V with chronic, repeated use
Systemic ¡V adrenal suppression can occur with
high dose, long-term treatment
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supervision of ophthalmologist
„h Increase IOP, aggravate glaucoma *monitor if admistered for 2 weeks
SELECT PARASITIC SKIN INFECTIONS
Condition Drug MOA Indication & ADRs/DDI/CI Specific Education/Other
Pediculosis/Lic
e
Pyrethrins &
piperonyl butoxide
Generally
work by
disruption of
nerve
conduction
„h Many are OTC, come in various dosage
forms, very specific instructions, specific
age limits
„h All drug tx + non-pharmacological tx
(combs, disinfestation of bedding/clothes)
„h Petrolatum ¡V good for eye lashes or
wanting to avoid pharmaceuticals
*Permethrin 1st line treatment ; Avoid use around eye, caution w/ ragweed or
chrysanthemum allergy
Benzyl Alcohol
Spinosad
Ivermctin
Malathion Use if resistance
Lindane NOT first line, black-box warning (CNS toxicity)
Scabies
Permethrin No use around eye, caution w/ ragweed or chrysanthemum
allergy
„h Tx bleeding, clotting and all infected
persons in household/institution!!
„h Itching persisting after initial eradication ¡V
use topical corticosteroid
Ivermectin Not FDA approved
Crotamiton High failure rates
ACNE MANAGEMENT
Class Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Topical
Retinoids
Tretinoin* Vitamin A analogs stimulate
epidermal cell turnover ¡V
unplug follicles, inhibit
inflammatory mediators
1st line in mild-moderate acne, combo
for moderate-severe, maintain
remission
ADR: skin (stinging, redness,
drying); Use sunscreen,
moisturizer, apply at night, avoid
use with benzoyl peroxide
most commonly used
Tazarotene more effective, but more irritation
*contraindicated in pregnancy
Adapalene less irritation, but less effective
Benzoyl Peroxide (OTC)
antibacterial and keratolytic often in combo with other antibiotics
to reduce resistance, OTC so often
used first-line as monotherapy
Pt Ed: can bleach of skin, avoid overuse (mostly once daily), do NOT
use with topical retinoids
ADR: skin (dryness and peeling of skin), well tolerated
Azelaic Acid (Rx)
normalizes keratinization
and suppresses P.acnes
less irritation, 1st-line for sensitive
skin, effective than other topicals,
indicated for Rosacea (specific form)
Pt Ed: reported cases of hypopigmentation, $$$
ADR: local skin irritation
Salicylic Acid (OTC)
desquamation of
hyperkeratotic epithelium,
keratolytic
less effective v. benzoyl peroxide, 2ndline
if other comedolytics haven¡¦t
worked, in combo with other agents
ADR: local skin irritation
Topical
Abx
Sulfacetamide increase turnover of
epithelium
failure of mild acne or moderate acne
(usually in combo Sulfacetamide + with other topicals)
Sulfur
Erythromycin
Clindamycin
Oral Abx Minocycline usually for moderate-severe acne,
given ~3 months/until under control
Dosed with topical retinoid
and/or benzoyl peroxide to
improve efficacy and reduce
resistance
Doxycycline
TMP-SMX
Azithromycin
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Erythromycin
Oral Contraceptives
estrogen is an anti-androgen
agent
moderate-severe acne (females only),
specific combos have indications
and/or are better for acne
Isotretinoin (Accutane)
Only for severe, recalcitrant, nodular
acne (extremely severe, failed other
tx), producing either physical/psych
scarring
***ORAL ISOTRETINOIN IS A POTENT TERATOGEN***
iPLEDGE program (anyone in contact w/ drug must use) ¡V only
prescribe 30 days/time, must complete monthly pregnancy test, etc.
ADRs: LOTS **must look up if you see on medication list, also a list of
lab tests to be ordered at baseline and during treatment
„h There is no cure, ranges mild„³severe, triggered by stress/sunlight/chemicals/etc; Strategy: topical retinoid „³ topical antibiotic „³ oral antibiotic „³ isotretinoin***
„h Don¡¦t forget patient expectations, address: discomfort, appearance, long-term scarring, psychological stress
„h Etiology: sebaceous gland hyperplasia, follicular hyperkeratosis, propionibcaterium acnes colonization, inflammation
ALLERGIC RHINITIS
Class Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Intranasal
Antihistamines
Azelastine Sneezing, rhinorrhea, nasal
pruritis, Olopatadine some congestion
PO 1st Gen
Antihistamines
*Diphenhydramine allergic/non-allergic rhinitis and
sleep
Allergic - photosensitivity, anaphylactic shock, drug rash, dermatitis
CV - postural hypotension, palpitations, reflex tachycardia, thrombosis at
injection site (IV promethazine)
CNS **- drowsiness, sedation, dizziness, coordination, fatigue, confusion
GI - epigastric distress, anorexia, bitter taste (nasal spray)
GU - urinary frequency, dysuria, urinary retention
Resp - chest tightness, wheezing, dry mouth, nose and throat, thickening
of bronchial secretions, epistaxis and nasal burning (nasal spray)
chlorpheniramine
clemastine
brompheniramine
hydroxyzine
PO 2nd Gen
Antihistamines
Desloratadine allergic/non-allergic rhinitis and
sleep
Allergic - photosensitivity, anaphylactic shock, drug rash, dermatitis
CNS* - somnolence/ drowsiness, headache, fatigue, sedation
Resp** - dry mouth, nose and throat (cetirizine, loratadine)
GI** - nausea, vomiting, abdominal distress (cetirizine, fexofenadine)
Fexofenadine
Levocetirizine
loratadine
cetirizine
Oral
Decongestants
Pseudoephedrine directly stimulate
alpha- and betaadrenergic
receptors
nasal/ophthalmic congestion,
Adjunctive/2nd Line
Oral: better used intermittently to
control symptoms
Topical: (max length of therapy is
generally 3 days due to rebound
congestion) ***IMPORTANT
**should not use long term
Phenylephrine
Topical
Decongestants
phenylephrine
naphazoline
tetrahydrozoline
oxymetazoline
Corticosteroids sneezing, rhinorrhea, itching, nasal
congestion **1st line therapy
Mast Cell
Stabilizers Comolyn Na OTC add-on therapy used for
prophylaxis, not for acute
ADR: burning, HA, unpleasant taste
CI: acute asthma attack
onset 1-2 weeks
Leukotriene
Receptor
Antagonist
Montelukast
Adjunctive/2nd Line ADRs: generally well tolerated
10
Intranasal
Anticholinergic
s
Ipratropium
bromide
rhinorrhea, Adjunctive/2nd Line Caution: gluaucoma, myasthenia
gravis, BPH (due to acetyl choline
receptors), urinary issues
Intranasal Saline (salt water, netti pots): help w/ congestion, moistening nasal passage
Special Populations: Pregnancy ¡V ipratropium*, budesonide, cromolyn; Elderly ¡V avoid anticholingerics, decongestants
SINUS/MOUTH/THROAT CONDITIONS
Rhinosinusitis
„h *Acute: 4 weeks, Chronic: 8 weeks, Recurrent: 3x per
year
„h Viral: common cold is #1 pathogen** (supportive only)
„h Bacterial: symptoms 10 days, 3+ days of severe fever,
purulent drainage, facial pain, worsening symptoms
„h Amoxicillin + clavulanate ; PCN allergy: doxycycline or FQ (levoflo/moxifloxacin)
„h Adjunct therapy: decongestants, corticosteroids, mucolytics, irrigation,
analgesics
„h Varies due to regional resistance rates, age, recent hospitalization, recent
antibiotic therapy, immune status
Strep
Pharyngitis
„h White exudates, edema, erythema, 10 days* „h 1st Line: PO PCN V, PO amoxicillin or IM penicillin
„h 2nd Line: Erythromycin (if PCN allergy), Azithromycin, Cephalosporins
Cold & Flu
„h Decongestant: Pseudoephedrine, Phenylephrine HCl
„h Expectorant: Guaifenesin
„h Cough Suppressant: Dextromethorphan HBr
„h Antihistamine: Doxylamine succinate, Diphenhydramine, Brompheniramine,
Chlorpheniramine
„h Pain/Fever: Acetaminophen, Aspirin, Ibuprofen, Naproxen
ORAL CANDIDIASIS
Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Fluconazole 1st line
Nystatin
Suspension
ADRs: N/V/D, poorly absorbed *swish & swallow (hold in mouth), relief in 24-
72hrs
Chlorhexadine
Gluconate
binds to bacterial and
yeast cell membranes
Symptom relief ADRs: staining of teeth protection ~6hrs
Magic
Mouthwash
MUST specify which EXACT ingredients you
want to be compounded
Clotrimazole
Troche
Tx or prophylaxis for patients on
chemotherapy, steroids, other IC
Needs special patient education
OTIC CONDITIONS
Condition Management
Acute Otitis
Externa
„h Clean canal: either manually or with 1:1 hydrogen peroxide/water **Only if TM intact!
„h Topical antibiotics: ofloxacin*, ciprofloxacin*, polymyxin B + neomycin, gentamicin, tobramycin (recall ototoxicity with AGs)
„h Antiseptics: act as bacteriostatic agents; alcohol is most common product
„h Glucocorticoids: hydrocortisone, dexamethasone (inflammation)
„h Acidifying agents: acetic, hydrochloric, sulfuric, boric (lower pH)
„h Mild: acidifying agent + glucocorticoid; Severe: antibiotic + antiseptic + glucocorticoid ** PO abx only for severe disease that extends outside of ear
canal
11
„h Patient education important: fill ear canal to expose for at least 20 minutes, protect ear canal from water
Malignant
Otitis Externa
„h 1st line IV antibiotics***(CBPs, AGs, anti-pseudomonal PCN) „³ systemic antibiotics + topical therapy
„h Targets: *Pseudomonas aeruginosa, Staphylococcus aureus
Acute Otitis
Media (AOM)
„h Treat symptoms: pain, fever + Treat Infection: 2 strategies *depends on severity and age
o Tx immediately w/ antibiotics, observe for symptom improvement within 48-72 hours
o Tx immediately w/ antibiotics: children 2 or 2 = appear toxic, otalgia for more than 48 hours, temperature 102, bilateral AOM, uncertain
follow-up care, immuno-compromised
„h First-line antibiotic choices:Amoxicillin, Amoxicillin-clavulanate (Augmentin); Alternatives: Macrolides, Clindamycin
„h Length of treatment: 2 years old treat for 10 days, 2 years old 5-7 days
Tinnitus Offending Medications: *Salicylates (aspirin), NSAIDs (ibuprofen, naproxen, diclofenac¡K), **Antibiotics (aminoglycosides, erythromycin, vancomycin), *Loop
diuretics (furosemide, bumetadine), Chemo drugs (cisplatin, vincristine)
GLAUCOMA/OPTHALMIC DRUGS
Class Drug MOA Indication ADRs/DDI/CI Specific Education/Other
Topical Prostaglandin
Analogs***
Increases aqueous outflow 1st line glaucoma
(recently)
ADR: increased brown pigmentation of the iris, eyelash growth, hyperpigmentation of
periorbital skin, conjunctival hyperemia, punctate epithelial keratopathy, foreign body
sensation, cystoid macular edema
Topical Beta-
Adrenergic Receptor
Reduces aqueous production Classically first
choice in
glaucoma
ADR: potential for systemic absorption is highest (bronchoconstriction, bradycardia,
depression, confusion, fatigue)
CI: obstructive airway disease
Topical Carbonic
Anhydrase Inhibitors
Reduces production of aqueous,
sulfonamide derivatives
Glaucoma ADR: local reactions including burning and stinging, superficial punctate keratopathy,
allergic reactions of the conjunctiva, bitter after-taste is common; systemic side effects
Topical Direct-Acting
Cholinergic Agonists
increase the outflow of aqueous
through the trabecular meshwork
Glaucoma ADR: local irritation, decreased vision
Topical Indirect-Acting
Anticholinesterase
Agents
Increase outflow of aqueous Glaucoma
Topical Corticosteroids
ADRs: exacerbation/development of microbial
keratitis, reactivation of herpes simplex keratitis,
ocular HTN, risk of open-angle glaucoma; cataract
Any patient receiving topical
corticosteroid therapy should be
under ophthalmologist
NSAIDS
block prostaglandin synthesis
through inhibition of
cyclooxygenase
pain and
inflammation
Miscellaneous Ocular Agents
„h Mydriatics and cycloplegics used to dilate and paralyze muscles of accommodation for inspection and/or procedures
„h Artificial tears/ocular lubricants used for symptoms of dryness
„h FYI: Other agents used by ophthalmologists such as immunologic agents
OPTHALMIC DRUGS & CONDITIONS
Condition Management
Blepharitis „h Warm compress (not hot)
„h Antibiotics: topical &/or systemic
12
o Topical: bacitracin, erythromycin oint
o Oral Tetracyclines (doxy- or mino-)
o Oral Macrolide: Erythromycin, Azithromycin
„h Topical anti-inflammatory agents: corticosteroids ointment, drops, cyclosporine 0.05%
Corneal Abrasion
„h Topical NSAIDS (reduce pain): diclofenac, ketorolac, nepafenac, bromfenac
„h Topical (prophylactic) antibiotics may be used b/c infection slows healing
o Discontinue contact lens use until healed
o Gentamicin or Fluoroquinolone (i.e. gati- or moxifloxacin)
Viral Conjunctivitis „h Antibiotics are NOT for viruses
„h Self-limiting : gets worse for 1 wk, then resolves in 2-3 wks
Bacterial Conjunctivitis „h Empiric treatment is broad spectrum
„h 1st line: polymixin B + bacitracin drops; erythromycin ointment ***SPECIFY EYE or OPHTHALMIC FORMULATION
EENT CONDITIONS REVIEW
System Conditions Management
Eye
Allergies
Application Conjunctivitis of liquid, ointment
Glaucoma
Ear Otitis Media
Cerumen Impaction
Nose
Allergies Nasal steroids: DOC, Antihistamines: 1st gen v. 2nd gen, Nasal antihistamines, LTRA, Ipratropium NS
Decongestants
Saline Irrigation
EENT REVIEW
Class Drug Comments
Intranasal
Corticosteroids
Beclomethasone
Budesonide
Ciclesonide Low systemic absorption
Flunisolide
Fluticasone Low systemic absorption
Fluticasone + Azelastine Combination of ICS and antihistamine
Mometasone Low systemic absorption
Triamcinolone
Systemic H1 Receptor
Antagonists
Chlorpheniramine OTC
Clemastine OTC
Cyproheptadine rarely for rhinitis, used more for urticaria, off-label for migraine prophylaxis
Diphenhydramine OTC
Hydroxyzine very sedating
Meclizine OTC formulations, used mainly for motion sickness and vertigo
Promethazine used for nausea and vomiting
13
Cetirizine OTC
Loratadine OTC
Desloratadine
Fexofenadine
Levocetirizine
Nasal H1 Receptor
Antagonists
Azelastine warn of drowsiness
Olopatadine warn of drowsiness
Opthalmic H1 Receptor
Antagonists don¡¦t need to know individual agents
14
PHARM FALL 2013 BLOCK II: ENDOCRINE & HEME
PITUITARY HORMONES
„h Posterior Hormones synthesized in neurons that originate in hypothalamus; Anterior Hormones synthesized in epithelial cells, but are under neural control via portal
circulation
„h Most require parenteral administration because of proteolytic breakdown in the gut; newer, synthetic analogues have PO stability; Many routes: IM, IV, SubQ, IN, PO
Class Drug MOA Uses/Coverage ADR/DDI
Posterio
r
Pituitary
Vasopressin
ADH: Controls rate of water excretion in urine
„h ¡ô = ¡ôpermeability, ¡õ water loss in urine
„h ¡õ = kidneys impermeable to water, ¡õ
reabsorption
Kidney: binds to V2 receptor to ¡ô water permeability
and reabsorption in collecting tubules; In liver, vascular
SM
Diabetes insipidus
Esophageal varices
Cardiac arrest/shock
ADR: Water intoxication, hyponatremia,
HA, bronchoconstriction, tremor
Caution: CAD, epilepsy, asthma, vascular
disease, elderly
Desmopressin Molecule modified for minimal activity at the V1
receptor
Diabetes insipidus and nocturnal
enuresis
Oxytocin
(Pitocin)
Oxytocin: Elicits Uterine contractions during labor, Milk
expression in lactation
Medical (not elective) induction of labor,
adjunct in abortion, postpartum bleeding
CI: fetal distress, abnormal fetal
presentation, premature births
Anterior
Pituitary
Corticotropin
ACTH: Stimulates production of glucocorticoids and
androgens by the adrenal cortex; maintains size of zona
fasciculata and zona reticularis of cortex
Dx: Diff. Cushing syndrome and ectopic
ACTH-producing cells, Diff. primary
(Addison disease) from secondary
adrenal insufficiency
Tx: MS, infantile spasms, other
inflammatory
ADR: like glucocorticoids (osteoporosis,
hypertension, edema, hypokalemia, CNS
stimulation, infection, etc.)
Cosyntropin Synthetic ACTH Diagnosis of adrenal insufficiency
Somatotropin
GH: Stimulates body growth; secretion of IGF-1;
stimulates lipolysis; inhibits actions of insulin on
car/lipid metabolism
GH deficiencies; is not indicated for use
in elderly to increase/maintain muscle
mass
ADR: edema (HTN, intracranial HTN, etc.),
neoplasms, bone malformations
Mecasermin IGF-I analogue
Tesamorelin GH secretagogue HIV-associated lipodystrophy
Pegvisomant GH Receptor Antagonist; prevents binding Tx-resistant acromegaly
Octreotide*
Somatostatin (GH inhibitor) Analog
Acromegaly, CA; diarrhea, esophageal
varices
Lanreotide Refractory acromegaly
Pasireotide Cushing¡¦s disease
Goserelin
GnRH Agonist:(Luteinizing hormone-releasing
hormone, gonadorelin): Endogenous GnRH undergoes
pulsatile secretion, release of FSH and LH is inhibited
Prostate cancer, endometriosis,
precocious puberty
CI: pregnancy
ADR women: hot flushes, sweating,
decreased libido, depression, ovarian cysts
ADR men: ¡ôtestosterone (bone pain); hot
flushes, *gynecomastia, edema, diim. libido
Histrelin
Leuprolide
Nafarelin
Triptorelin
Degarelix
GnRH Antagonist
Advanced prostate cancer
Cetrorelix Control ovulation CI: Preg category X
Chorionic FSH: development of ovarian follicles; regulates Infertility treatment in women and men;
15
Gonadotropin spermatogenesis in testis
LSH: ovulation and formation of the corpus luteum in
the ovary; stimulates production of estrogen and
progesterone, testosterone
specialist use only
Follitropin B
Follitropin A
Urofollitropin
Prolactin Prolactin: Stimulates milk secretion and production
Stimulate and maintain lactation,
Decrease sex drive and reproductive
function
THYROID HORMONES
„h Iodine is brought into glanda Thyroid hormones are made in gland a thyroid hormones and exported out of gland into circulation.
Class Drug MOA Uses/Coverage ADR/DDI
Antithyroi
d
Methimazole Inhibits thyroid hormone synthesis Hyperthyroidism/Grave¡¦s
disease
ADR: Dermatitis*, myalgia, arthralgia, jaundice, edema; nephritis,
agranulocytosis*, hepatotoxic*
CI: Preg Cat D
PTU
Propylthiouraci
l
Inhibits T3/T4 synthesis; iodination of
tyrosyl groups and condensation of
iodotyrosines to form T3 and T4
Hyperthyroidism/Graves
disease
BBW: hepatotoxicity
ADR: Derm, GI, arthritis; Granulocytopenia, leukopenia
CI: Preg Cat D, max 200mg/d
Iodide
Inhibits the iodination of tyrosines;
inhibits T3/T4 release from
thyroglobulin
Only for short term/3rd
line (thyroid storm, presurgery)
Potassium
Iodide
iIhibits thyroid hormone synthesis and
release Hyperthyroidism
ADR: metallic taste, GI; arrhythmias, GI bleed, goiter, angioedema
CI: Hyperkalemia, severe dehydration, hypothyroidism, renal
impairment Preg Cat D
Beta
Blocker Propanolol
Non-selective beta antagonist (B1 &
2); Partially block conversion of T4 to
T3 Graves symptomatic tx
ADR: dizzy, bradycardia, hypoTN, impotence; bronchospasm
BBW: Abrupt D/C„³ angina exacerbation, MI, arrhythmias
CI: cardiogenic shock, sinus bradycardia; Pregnancy precaution
Precaution: Bronchial asthma, DM, uncompensated HF; Abrupt
withdrawal
CCB Diltiazen Calcium channel blocker Graves 2nd line
symptomatic
Thyroid
Hormone Levothyroxine Hypothyroidism
CI: acute MI, thyrotoxicosis, adrenal insufficiency
ADR: appetite increase, tachycardia, wt loss, nervousness, insomnia,
heat intolerance, tremor; arrhythmias, CHF, HTN, angina
16
INSULIN
„h Standard insulin concentration is 100 units/mL *This is done to reduce confusion and chance for errors in dosing
Class Drug Uses/Coverage ADR PK/Education
Rapid Acting
Insulin Lispro Diabetes ADR:
„h Most common and potentially most lifethreatening:
hypoglycemia***
„h Other common: Weight gain,
Lipodystrophy, Allergic reactions, Injection
site reactions
Combine with basal, can be IV or pump. MUST eat,
Insulin Aspart use 15 ac¡V15 min pc
Insulin Glulisin
Short Acting Regular Insulin (Novolin) Diabetes 30-60min ac, coordinate meals in advance
Intermediat
e Acting
NPH Basal control, never IV, not for emergencies
Protamine Diabetes
Long Acting
Glargine Diabetes Avoid mixing, never IV
Detemir
NON-INSULIN
Class Drug MOA Uses/Coverage ADR/DDI PK/Education/Other
Sulfonylureas
Glimepride Stimulate insulin secretion
by blocking K channels „³
„^Ca+
Diabetes ADR: Hypoglycemia, weight gain,
hepatic/renal
Serum protein bound, P450
Glipizide metabolism
Glyburide
Meglitinides
Nateglinide Same as SU with rapid
action, short duration
Diabetes post-prandial ADR: Hypoglycemia, hepatic/renal PO ac 1-30 min, P450 metabolism
Repaglinide
Metformin Reduce gluconeogenesis Diabetes 2 DOC ADR: GI!!!
BBW: Lactic acidosis, Cr 1.5
PO
TZD Pioglitazone Increase insulin sensitivity Diabetes 2nd/last line ADR: Edema, liver failure, anemia
BBW: Heart failure
PO, „^serum bound, „^P450 metabolism
17
ĄGlucosidase
Inhibitor
Acarbose Delay carb digestion Diabetes ADR: GI!!! Flatulence Take with first bite
Miglitol
DPP4
Inhibitors Gliptins Block incretin break down Diabetes ADR: Hypersensitivity, pancreatitis, $$$ PO + combo, adjust dose if
renal/hepatic
SLGT2
Inhibitor Invokana
„` glucose reabsorption in
renal tubules
Diabetes ADR: Glucosuria, CI in renal, lots of DDIs
(kidneys)
BBW: Avoid in diabetes gastroparesis
Amylin Analog Pramlintide
„` gastric emptying and „`
glucose
Diabetes ADR: Hypoglycemia, GI *do not mix in
syringe
BBW: Thyroid tumors in animals
GLP-1 Analogs
Exenatide Incretin mimics, „` gastric
emptying
Diabetes ADR: GI, pancreatitis
Liraglutide
ANEMIA TREATMENT
Anemia Goal Class/Type Drugs ADR/DDI Education/Other
Iron Deficiency
Replenish
iron stores
(measure
Hgb and Hct
in about 2-4
weeks to
check trend)
****First
treat cause
Oral Iron
Ferrous gluconate ADR: dyspepsia, NVCD, dark stools
DDI:
¡E H2 Blockers, PPIs, antacids ¡õ absorption (take
1hr pre or 4h post antacid
¡E Tetracyclines & Quinolones¡õ absorption
¡E ¡õ absorption of thyroid hormones
¡E Ca salts: ¡õ absorption
¡E Vitamin C: ¡ô absorption
¡E Take on empty stomach (~1hr ac)
¡E Continue 3-6mo after to build up stores
Ferrous sulfate ¡E DFI: food ¡õ absorption
Ferrous fumerate
Carbonyl iron
Parenteral
Iron
*just need to
know IV exists!
ADR:
¡E **Anaphylactoid reactions: give test dose prior
to infusion
¡E Delayed reactions (2-7 days) can occur: Fever,
urticaria, arthralgias, lymphadenopathy
¡E Others: chest pain, headache, hypotension,
n/v/d, abdominal cramping
Indications: Fail PO iron, Intolerance to PO iron,
Required antacid therapy, Significant blood loss
but patient refuse blood transfusion, Chronic
hemodialysis
Vit B12
Deficiency
Replenish
B12
Diet High Vit B12: Beef liver, cereal, trout, salmon, beef
Low Vit B12: clams, oysters, tuna, milk
Oral B12
OTC Cobalamin ADR: HA, NVD, hypoK
Monitor: 1-2mo post initiation, then Q6-12mo
For pt w/o neurologic sxs
SubQ/IM For pt w/ neurologic sxs
18
QD x 1wk, then Qwk x 1mo, then Qmo
Folic Acid
Deficiency
Replace
body stores Folic Acid 1mg QD
Pregnancy Folic Acid 0.8mg QD
Replenish
diet Diet Liver, cereal, lentils, chickpeas, asparagus, spinach, black beans, pasta¡K.
Anemia of
Chronic
Disease
Epoetin alpha
BBW: ¡ô CV risk (death) in CRF pts, ¡ô risk of death &
tumor progression in CA pts, ¡ô risk of
thromboembolic events in surgery pts
CI: uncontrolled HTN, Ab-mediated anemia
ADR: HTN, edema, tachycardia, NVD, thrombosis
Serious ADR: tumor progression, ¡ômortality, CHF,
stroke, MI, seizure, embolism
Subcutaneous or IV; Dose depends on Dz (CRF,
HIV, Chemo, surgery¡K), Hospital formulary
Target Hgb 10-12gm/dL
„h ¡ô dose 25% if Hgb response 1gm/dL after
4wk or Hgb 10gm/dL
„h ¡õ dose 25% if Hgb response 1gm/dL
within 2wks or Hgb nears 12gm/dL & still
¡ô¡Khold
Darbepoetin
alpha
ANTIPLATELETS
Platelet Aggregation Inhibitors:
„h Prevention and treatment of occlusive cardiovascular disease
„h Maintenance of vascular grafts and arterial patency
„h Adjuncts to thrombin inhibitors or thrombolytic therapy in myocardial infarction
Class Drug MOA Uses/Coverage ADR/DDI PK/Education/Other
COX-1
Inhibitor
Aspirin Inhibits
thromboxan
e A2
synthesis
from
arachidonic
acid by
irreversible
acetylation
of a serine
on COX-1
„h Prophylactic treatment of
transient cerebral ischemia
„h Reduce the incidence of
recurrent MI
„h Decrease mortality in pre- and
post-MI
„h Other (anti-inflammatory)
Warning/caution uses:
„h Salicylate sensitivity (avoid ASA); Increased in
patients with asthma and nasal polyps
„h EtOH/elderly/surgical: increase bleeding risk
„h Peds: avoid ASA with viral illnesses (Reyes)
ADRs (all increase with higher doses): ¡ôbleeding
time: ¡ôrisk for hemorrhagic stroke, ¡ôrisk for GI
bleeding; GI upset/ulcers, Anaphylaxis, urticaria,
hypersensitivity; CNS: confusion, MS changes, coma
(toxic doses); Tinnitus; Renal impairment (ALL
NSAIDs)
DDI: NSAIDs (dose ASA at least 30 min before or 8 h
Effects of ASA lasts for the life of
the platelet (7-10 d); Repeated
admin of ASA has a cumulative
effect on the function of platelets
*Most common dose in US is 81
mg/d (formerly ¡§baby aspirin¡¨) and
is often called ¡§low-dose aspirin¡¨
19
after), **Many other (anything that can affect
bleeding will increase risk and thus cause a DDI)
*NOTE: ASA is only NSAID with irreversible
antithrombotic efficacy
ADP
Receptor
Inhibitor
s
Ticlopidine
Irreversibly
inhibit the
binding of
ADP to
receptor on
platelets
thus
inhibiting
GP IIb/IIIa
receptor
activation
Prevention of TIAs and strokes for
pts with prior cerebral thrombotic
event, Adjunct therapy with ASA
following coronary stent *Reserve
use in patients who are intolerant
to other therapies
BBW: May cause life-threatening hematologic
reactions, including neutropenia, agranulocytosis,
thrombotic thrombocytopenia purpura (TTP), and
aplastic anemia
Caution/warning uses: Increases bleeding risk;
Elderly avoid if possible
¡E Food interferes with ticlopidine
¡E All are extensively bound to
plasma proteins
¡E They undergo hepatic
metabolism by CYP450 to active
metabolites
¡E Max effect in 3-5 days and effect
can persist* if drug is dc¡¦d
¡E Elimination of the drugs and
active metabolites occurs by
both renal and fecal routes
¡E All these drugs increase risk for
prolonged bleeding for which
there is no antidote
PLAVIX
Clopidogrel
Atherosclerosis prevention after
MI, stroke, PAD; Thrombotic
prophylaxis in ACS and events
associated w/ PCI with or without
stent; Preferred over ticlopidine in
ischemic disease
ADRs: Fewer than ticlopidine but still slight risk of
same hematologic reactions
BBW: higher rate of cardiovascular events following
MI or stent thrombosis following PCI.
Prasugrel
Reduces rate of thrombotic
cardiovascular events in patients
managed with PCI for UA, STEMI,
or NSTEMI
BBW: Fatal bleeding risk, Use in patients 75+ years
old due to risk of intracranial bleeding, Do not
initiate in those likely to undergo coronary artery
bypass graft (CABG) and stop at least 7 days prior to
other surgeries
Ticagrelor
Conjunction w/ ASA for secondary
prevention of thrombotic events
UA, NSTEMI, STEMI managed
medically or with PCI and/or CABG
BBW: Fatal bleeding risk, Avoid high-dose ASA use
due to inactivation of ticagrelor, Avoid initiation of
when urgent CABG surgery is planned; when
possible, discontinue use at least 5 days before any
surgery
DDI: major CYP3A4 substrate
GP
IIb/IIIa
Inhibitor
s
Abciximab
Blocks
binding of
fibrinogen
and von
Willebrand
factor
Prevention of cardiac ischemic
complications in PCI patients or
UA/NSTEMI unresponsive to
conventional therapy when PCI is
scheduled within 24 hours
ADR: Bleeding risk, anaphylaxis (has mouse bits!) Dosed IV along with ASA or heparin
Antiplatelet effects persist up to 72
hours
Eptifibatide
Cyclic
peptide
blocks
receptors
Treatment of ACS, including
patients managed medically and
PCI
ADRs: bleeding risk Dosed IV
Duration of action: ~4h
Tirofiban Blocks
receptors
Treatment of ACS ADRs: bleeding risk Dosed IV with heparin
Duration: 4-8h
Phosphodiesterase
Inhibitors
Dipyridamole Causes an
accumulatio
n of
adenosine,
Labeled Indications:
Oral: Used with warfarin to
decrease thrombosis in patients
after artificial heart valve
ADRs: bleeding risk, orthostasis (especially elderly) Use of aspirin/extended release
dipyridamole is recommended
20
adenine
nucleotides,
and cAMP;
stimulate
release of
prostacyclin
; Causes
coronary
vasodilation
replacement
I.V.: Diagnostic agent in CAD
(Persantine Stress Test)
Unlabeled: Stroke prevention
Cilostazol
Sx management of peripheral
vascular disease, primarily
intermittent claudication
BBW: use in HF
DDI: many w/ hepatic metabolism
ANTICOAGULANTS
Class Drug Uses/Coverage ADR/DDI PK/Education/Other
Unfractioned
Heparin UFH
Binds to antithrombin and accelerates its action to
irreversibly inactivate the following: ***Factor IIa
(thrombin), ***Factor Xa, Factor IX, Factor XI, Factor
XII; Inhibits platelet function, Increases vascular
permeability
ADR:
¡E Bleeding complications: Hemorrhage ¡V
requires careful monitoring * Antidote
for heparin is protamine sulfate
¡E Hypersensitivity ¡V heparin isolated
from animal sources so can be
antigenic
¡E Thrombosis ¡V chronic or intermittent
administration can lead to reduction
in antithrombin III activity a
thrombosis
¡E Thrombocytopenia ¡V associated with
UFH much more than LMWHs (HIT,
monitor platelet count frequently)
¡E Other: abnormal liver function testing;
Osteoporosis with long-term
CI: Hypersensitivity, Bleeding disorders,
Alcoholics, Having or have had recent
surgery of the brain, eye, or spinal cord
Dosing: Continuous IV infusion
preferred, or SubQ
Monitoring: aPTT is used to titrate
doses
LMWH
Dalteparin
Differences vs. UFH:
¡E Molecular wt
¡E Antithrombotic properties
¡E PK properties
¡E ADRs (fewer thromboembolic)
¡E Monitoring requirements
Enoxaparin
Tinzaparin
Factor Xa
Inhibitors
Fondaparinux
¡E IV & SubQ
¡E Prophylaxis of DVT after hip/knee replacement,
hip fracture surgery, or abdominal surgery
¡E Treatment of acute PE
¡E Treatment of acute DVT without PE
¡E Off-label: treatment of HIT
ADR: Bleeding is main problem
BBW: Discontinuation leads to risk of
stroke so need to add other anticoagulant
therapy; Neuraxial anesthesia: spinal or
epidural hematomas (bleeding into spinal
cord with procedures)
Warnings: Renal impairment, Liver
disease, Elderly
Advantages:
¡E Well absorbed via SubQ route
¡E Predictable PK profile (F,
elimination)
¡E Less monitoring (often none)
Rivaroxaban
¡E PO**
¡E Post-op thromboprophylaxis after hip/knee
replacement
¡E Prevention of stroke and systemic embolism in
patients with nonvalvular Afib
Apixaban ¡E PO
¡E Nonvalvular Afib to prevent stroke and systemic
21
embolism
Direct
Thrombin
Inhibitors
Argatroban IV to treat HIT, adjunct in PCI in pt with risk or h/o
HIT
Bivalirudin
+ ASA in UA undergoing PCTA or PCI w/ GP IIb/IIIa
inhibitor or patient undergoing PCI with (or risk of)
HIT
Dabigatran 1 s t PO anticoagulant since warfarin; stroke
prevention
ADR: Bleeding, GI upset Advantages: No routine monitoring,
Fewer DDI v. warfarin, Predicable PK
Desirudin DVT prophylaxis in pts undergoing hip replacement
Lepirudin IV to treat HIT, adjunct in PCI in pt with risk or h/o
HIT
Vitamin K
Antagonist Warfarin
MOA: Hepatic synthesis of coagulation factors II, VII,
IX, and X, as well as proteins C and S, requires the
presence of vitamin K.
Prophylaxis and tx of thromboembolic disorders and
complications from Afib or valve replacement,
adjunct to reduce risk of systemic embolism after MI
CI: Hemorrhagic tendencies; Recent
eye/CNS surgery; uncontrolled malignant
HTN; Pericarditis/PE, bacterial
endocarditis; Unsupervised patients, high
potential for noncompliance; Preeclampsia/
eclampsia
BBW: fatal bleed ( 65yo, INR 4, HTN,
DM, open wounds)
Preg: X
DDI: ¡ô Bleed: ASA, clopidogrel,
dipyridamole, NSAIDs, heparins; ¡õ INR: Vit
K, sucralfate, barbitals, rifampin,
phenytoin, nafcillin, griseofulvin,
cholestyramine, carbamazepine; ¡ô INR:
APAP, EtOH, allopurinol, amiodarone,
chloral hydrate, cimetidine, fenofibrate;
FQs, Cephalosporins, , -azole antifungals,
omeprazole, sulfamethoxazole, Influenza
vaccine, vitamin E
¡E ID of dose/tablet/brand
¡E Need for regular monitoring
(danger if missed)
¡E Inform all healthcare providers of
use
¡E S/Sx of bleeding
¡E Missed doses
¡E Diet/EtOH
¡E OTC meds/herbals
¡E Dose same time daily
Thrombolytics
Alteplase MOA: Modified forms of tPA that bind to fibrin and
covert plasminogen to plasmin; used in STEMI
Other use: Massive PE, Ischemic stroke, Open central venous access devices
Reteplase
Tenecteplase * Might offer advantages due to fewer noncerebral bleeding events and ease of use
(single bolus dose)
22
PHARM FALL 2013 BLOCK III: CARDIOLOGY
ANTIARRYTHMIA DRUGS
Goal: decrease HR by interrupting ion channel function (Decrease phase 4 slope, Increase threshold potential, Increase max diastolic potential, Increase AP duration)
Proarrhythmic by nature**
Class Drug Comment
(I) Sodium Channel
Blockers MOA: „`phase 0, prolong phase 3
(II)
Beta Blockers
Propanolol
MOA: Inhibit Metoprolol sympathetic activity
Esmolol
(III) Potassium Channel
Blockers
Amiodarone
MOA: Prolong phase 3
Dofetilide
Dronedarone
Sotalol
(IV) Calcium Channel
Blockers
Diltiazem
Verapamil MOA: Slow conduction at SA/AV nodes, prolong phase 3
Other
Adenosine Used for SVT (IV w/ very short . life)
Digoxin Used for AFib, „^vagal tone
HYPERLIPIDEMIA DRUGS
PATIENTS WHO NEED A STATIN:
1. 75YO W/ CLINICAL ASCVD W/ HIGH-INTENSITY OR 75YO W/ CLINICAL ASCVD W/ HIGH-MODERATE INTENSITY
2. ANY AGE LDL 190 W/ HIGH-INTENSITY
3. 40-75YO W/ DM & LDL 70 BUT NO ASCVD W/ MODERATE INTENSITY OR HIGH FOR THOSE WITH 10 YR ASCVD RISK 7.5%
4. 40-75YO W/O DM OR ASCVD AND LDL 70 & HAVE 10 YR RISK OV ASCVD 7.5% W/ MODERATE TO HIGH INTENSITY
Class Drug MOA Uses/Coverage ADR/DDI PK/Education/Other
Statins
Atorvastatin
or
Rosuvastatin
for high
intensity
Inhibit cholesterol synthesis in liver
leading to increased LDL receptors
and increased cholesterol uptake in
the blood
*DOC for
Hyperlipidemia
ADR: Hepatic, MSK (strains, sprains, myalgias),
CNS, Cataracts
DDI: CYP3A4 Substrate (Warfarin, Protease
inhibitors, Macrolides, Fibrates, Azoles)
CI: Pregnancy, Breastfeeding, Active Liver Disease
Monitor: Baseline (CK, LFT,
Lipid, Renal) + Lipid q4-8w
until stable + Lipid q6m
Dose: qhs, alternate date
dosing to reduce myalgias
Niacin Niacin Rx
Inhibits lipolysis in adipose tissue
(liver cannot make LDL) and also
increases tPA and decreases plasma
fibrinogen
*Most potent to
raise HDL
ADR: cutaneous flushing + pruritus (Dose qhs +
ASA); N/V, impaired glucose tolerance, Hepatic
Caution using with (*Statin)
Fibrates
Fenofibrate
Decrease VLDL/TG, Increase HDL * Works best
on TG
ADR: N/V/D/C, gallstones
DDI: Statin (myopathy, rhabdomyolysis),
Warfarin, all cardiac Rx
CI: kidney/liver disease, gallbladder disease,
biliary disease, pregnancy, breastfeeding
Basically CI in pts with HTN
or any cardiac dz due to
DDI
Fenofibric Acid
Gemfibrozil
Bile Acid Cholestyramine Resins bind bile acids and cholesterol ADR: GI (N/V/C/F), impaired absorption
23
Sequestrant
s complex is excreted in feces DDI: Impaired drug absorption (Dose 1-2h pre- or
4-6h post- other meds)
Colesevelam
Colestipol
PCSK9
Inhibitors
Alirocumab
Evolocumab
Rx revents PC5K9from degrading LDL
receptors in liver increasing # of
LDLR¡¦s available to clear LDL
Familial
Hyperlipidemia
& have failed
max dose of
statin
Mouse bits! $$$$$, SubQ only
Cholesterol
Absorption
Inhibitors
Ezetimibe Inhibit cholesterol absorption at
brush border of small intestine
*Adjunct Use
Only
ADR: GI, Heptatic (caution w/ Statin)
Omega 3
Fatty Acids
Icosapent ethyl
O3 ethyl ester
O3 carboxylic
acid
Decrease synthesis of VLDL-TG *Adjunct Use
Only
Rx Omega 3 $$$$
ANTIANGINAL DRUGS
Angina Management: *Determine Type
¡E Antianginal + ASA + Clopidogrel + Others
¡E Lifestyle modification
Acute Coronary Syndrome Management:
¡E ER Treatment: Morphine, Oxygen, NTG, ASA, BB
¡E Long-term management: BB, ASA, Statin, Antiplatelet + Lifestyle modification
Class Drug MOA Uses/Coverage ADR/DDI PK/Education/Other
Organic
Nitrates
NTG
Release NO to
induce systemic
vasodilation
*DOC for Acute Angina
IV: acute angina, acute MI, perioperative HTN
SL: acute angina, prophylaxis
Transdermal/Ointment: prophylaxis
ADR: HA, HypoTN, facial
flushing; Patient education on
12-14h/d of nitrate free intervals
DDI: PDE-5 Inhibitors (Sildenafil,
Tadalafil, Vardenafil)
Isosorbide
mononitrate
Isosorbine
dinitrate
Beta-
Adrenergic
Antagonists
Block
sympathetic
stimulation
*DOC in prophylaxis of Chronic Stable Angina
unless CI (adjunct use for Variant Angina)
CI: asthma, COPD, severe
bradycardia, PVD/vasospastic
disease, DM, depression
24
Calcium
Channel
Blockers
Diltiazem
Slow contraction
in smooth
muscle of heart
*Adjunct for Stable/Variant if uncontrolled or CI
Verapamil *Verapamil: CI in AV conduction
abnormality
Amiodipine
Felodipine
Sodium
Channel
Blockers
Ranolazine PO prolong phase 3
(repolarization) *Last line for Chronic Angina
DDI: Lots!
ANTI-CHOLINERGIC DRUGS
Class Drug MOA
Antimuscarini
c Atropine MOA: Bind to ACh receptors but do not trigger usual
response; Blocks parasympathetic system to „^HR
**drugs have many more therapeutic uses
CV Use: blocks parasympathetic activity to cause HR
increase (dose-dependent reaction)
Other Use: eye (mydriasis, unresponsiveness to
light), OP poisoning, pre-anesthesia secretion drying
ADR: Anti-SLUDGEMM, Anti-DUMBBELSS
Ganglionic Blocker
Neuromuscular Blocker
ADRENERGIC/CHOLINERGIC AGONIST DRUGS
Class Drug MOA Uses/Coverage ADR/DDI/CI
Direct-Acting
Adrenergic
Agonists
Epinephrine
MOA: ƒÒ1, ƒÒ2 low doses, ƒÑ1, ƒÑ2 at high doses
Action: „^BP/HR/contractility,
bronchodilation
Use: bronchospasm, anaphylactic shock,
cardiac arrest, anesthesia adjunct; Rapid
onset, brief duration (IV in ER)
ADR: CNS, hemorrhage, arrhythmia,
pulmonary edema
CI: hyperthyroid, cocaine, DM, BB use
Norepinephrine
(Levophed)
MOA: some ƒÒ1, mostly ƒÑ1 & ƒÑ2
Action: „^BP, baroreceptor reflex
Use in shock **do NOT use in allergic
reaction!
ADR: similar to Epi + skin
blanching/sloughing along injected vein
Isoproterenol MOA: predominantly ƒÒ1 & ƒÒ2 effects (nonselectivity
is major drawback)
Use: some cardiac testing or ER heart
stimulation, rare
Dopamine MOA: ƒÒ1 at low doses, ƒÑ1 at high doses, Use: cardiogenic/septic shock in CKD, CHF,
25
dopaminergic HOTN *Good if increased flow to kidneys
needed
Dobutamine MOA: stimulates ƒÒ1 receptors to „^HR and
CO (few vascular effects)
Use: cardiac decompensation, cardiac
surgery, acute HF
ADR: same as Epi, *caution in AFib due to
„^AV conduction
Clonidine MOA: CNS acting Ą2 agonist (blocks NE) Use: chronic HTN
Fenoldopam MOA: Ą2 & peripheral D-1 Dopamine
receptor agonist
Use: severe HTN (ER); 6x more potent
than Dopamine
Oxymetazoline MOA: Ą1 agonist Use: eye/nasal vasoconstriction
Phenylephrine MOA: Ą1 agonist Use: nasal vasoconstriction
ƒÒ2 Agonists (-
erols)
MOA: ƒÒ2 agonists (bronchodilation)
Use: bronchospasm
Indirect-
Acting
Amphetamine
Cocaine
Mixed-Action
Ephedrine
Pseudoephedrine
ADRENERGIC ANTAGONISTS
Class Drug MOA Uses/Coverage ADR/DDI
Ą-Antagonists
(Sympatholytics
)
Doxazosin MOA: block Ą receptors to reduce
sympathetic („`PVR, reflex tachycardia)
Action: SM vasodilation, profound
orthostatic HOTN („`1st dose, dose qhs)
Profoundly „`BP, use in HTN+BPH and
pheochromocytoma
ADR: HOTN, dizziness, fatigue, nasal
congestion, Prazosin HA, sexual dysfunction
Terazosin
Nonselective
ƒÒ-Antagonists
Propanolol Action: „`HR/contractility, „`SA/AV
conduction, „`CO/O2 consumption,
peripheral vasoconstriction (paradox),
bronchoconstriction, „^Na+ retention BC
OF DROP IN BP
Use: HTN, migraine, hyperthyroid, angina,
MI
ADR: bronchoconstriction (COPD),
arrhythmia, sexual, metabolic, CNS
DO NOT USE IN PTS WITH RESP DZ! CAN
ALSO MASK SSX OF HYPOGLYCEMIA!!
Do not stop Dx suddenly- may cause
arrhythmia!
Nadolol- potent,
used by Cardio
MD
Timolol- topical
for glaucoma
Selective
ƒÒ1-Antagonists
Atenolol Developed to eliminate unwanted bronchoconstriction, BUT selectivity is lost at high
doses! Use in HTN with impaired pulmonary, DM
Educate pts with respiratory dz!
Bisoprolol,
Metoprolol
succinate
Nonselective
w/ ISA
Penbutolol MOA: stimulate ƒÒ receptor but inhibit
stimulation by catecholamines and result
in diminished effect of HR/CO
Use: HTN with bradycardia or DM
Pindolol
Selective w/ ISA Acebutolol
ƒÑ&ƒÒ
Antagonists
Carvedilol MOA: concurrent blocking produces
peripheral vasodilation
Use: HTN if vasoconstriction is undesirable
(CHF)
Does not alter lipid or glucose levels due
Labetalol to B1 selectivity
26
DIURETICS
Class Drug MOA Uses/Coverage ADR/DDI PK/Education/Other
Thiazide
Diuretics
Hydrochlorothiazid
e
MOA: block Na/Cl symporter
in DCT to cause Na/H2O
retention (loss)
*DOC in HTN, most widely
used Use: HTN, HF,
hypercalciuria, DI („^K/Mg
excretion, „`Ca/UA excretion)
ADR: HOTN, hypokalemia,
hyponatremia, hyperuricemia,
hypercalcemia, hyperglycemia,
hypersensitivity, volume
depletion
PK: PO, sulfa derivative (CI if
allergy), ceiling effect, renal
Chlorothiazide activation
Chlorthalidone
Indapamide
Metolazone
Loop
Diuretics
Bumetanide MOA: block Na/K/Cl uptake in
TALH to cause Na/H2O
retention (loss)
STRONGEST DIURETIC
Use: edema, hypercalcemia,
hyperkalemia („^K/Mg/Ca/H/UA
excretion) *DOC in edema,
remove lots of fluid!
ADR: HOTN, hypokalemia,
hyponatremia, hypocalcemia,
alkalosis, ototoxicity (AG), GI,
hypersensitivity, DDI w/
diuretics, digoxin, BB, AG
PK: IV/PO, fast onset (ER), high
ceiling= INCREASE DOSE =
MORE DIURESIS, renal
excretion
Furosemide
Torsemide
K+ Sparing
Diuretics
Amiloride MOA: block aldosterone (S/E)
and block Na channel (A/T) in
DCT
Use: HTN, CHF, ascites
(cirrhosis), aldosteronism,
hypokalemia, remodeling
*Always adjunct use in anti-
HTN
ADR: hyperkalemia, sexual
Eplerenone dysfunction (S)
Spironolactone
Triamterene
Carbonic