• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/138

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

138 Cards in this Set

  • Front
  • Back
  • 3rd side (hint)
Carbamazepine
Type: Neuropathic Pain Anti-convulsant

Mechanism: Glutamate antagonist

Use: Pain relief, Epilepsy; Bipolar disorder

SE: Autoinduction of metabolism; Granulocyte suppression; Aplastic anemia; rash
Neuropathic Pain Anti-convulsant
Lamotrigine
Type: Neuropathic Pain Anti-convulsant, Mood Stabilizer

Mechanism: Glutamate antagonist

Use: Pain relief, Epilepsy; Bipolar disorder

SE: Autoinduction of metabolism; Granulocyte suppression; Aplastic anemia; rash
Neuropathic Pain Anti-convulsant, Mood Stabilizer
Nortriptyline
Type: Neuropathic Pain, Tricyclic Antidepressant (TCA)

Mechanism: NE and serotonin Reuptake inhibitor

Use: Rapid pain relief; depression

SE: Anti-muscarinic, anti-histaminergic, anti-adrenergic; Dry mouth, blur, confusion, sedation, hypotension; sexual dysfunction, seizures, myocardial depression
Neuropathic Pain, Tricyclic Antidepressant (TCA)
Propanolol
Type: Anti-migraine, anxiolytic, anti-angina/HTN

Mechanism: Beta-Blocker

Use: Pain relief - preventative. Used with nitrates, decreases HR, which decreases cardiac O2 demand and BP. Anxiety

SE: Can trigger bronchospasm in asthmatic pts; masks hypoglycemia
Anti-migraine, anxiolytic, anti-angina/HTN
Probenecid
Type: Uricuric agent

Mechanism: Increase urate excretion (prevents reabsorption)

Use: Acute gout

SE: GI irritation, rash
Uricuric agent
Diazepam
Type: Benzodiazepines

Mechanism: Allosterically enhance binding of GABA

Use: Preoperative Meds (lowers anxiety). Generalized anxiety, panic, seizure,muscle relaxation. Anti-convulsant (status epilepticus)

SE: Drowsiness, ataxia, impaired judgment, tolerance
Benzodiazepines
Lorazepam
Type: Benzodiazepines

Mechanism: Allosterically enhance binding of GABA

Use: Preoperative Meds (lowers anxiety). Generalized anxiety, panic, seizure,muscle relaxation. Anti-convulsant (status epilepticus)

SE: Drowsiness, ataxia, impaired judgment, tolerance
Benzodiazepines
Morphine
Type: Opioid

Mechanism: mu receptor agonist

Use: Preoperative Meds (sedation); schedule II

SE: Constipation
Opioid
Nitrous Oxide
Type: Inhalation Anesthetic

Mechanism: Volume expansion theory; non-specific effects at specific cell receptors

Use:

SE: malignant hyperthermia; increase in HR, unstable BP; muscle rigidity and cyanosis (antidote - dantrolene, muscle relaxant
Inhalation Anesthetic
Cocaine
Type: Sympathomimetic

Mechanism: Blocks reuptake of NE

Use: Local anesthetic: topical - rapid onset and short duration; Used with epinephrine (keeps drug localized by constricting BV's); schedule II

SE: Drowsy, tired, fuzzy thinking, blur, muscle pain, Higher incidence of allergic RXN
Sympathomimetic
Baclofen
Type: Antispasmodic agents

Mechanism: Action on spinal reflexes (GABA agonist)

Use: Treatment for MS, cerebral palsy, spinal injury, stroke

SE: Myalgias; increased IOP, intraabdominal and ICP; malignant hyperthermia (succinyl); histamine release
Antispasmodic agents
Dantrolene
Type: Antispasmodic agents

Mechanism: Directly-acting (RyR antagonist)

Use: Muscle relaxant; antidote for malignant hyperthermia

SE: Myalgias; increased IOP, intraabdominal and ICP; malignant hyperthermia (succinyl); histamine release
Antispasmodic agents
Metaxalone
Type: Antispasmodic agents

Mechanism: CNS depressant

Use: alleviate spasms associated with MS, cerebral palsy, stroke, or spinal injury

SE: Myalgias; increased IOP, intraabdominal and ICP; malignant hyperthermia (succinyl); histamine release
Antispasmodic agents
Tizanidine
Type: Antispasmodic agents

Mechanism: alpha-2 agonist

Use: alleviate spasms associated with MS, cerebral palsy, stroke, or spinal injury

SE: Myalgias; increased IOP, intraabdominal and ICP; malignant hyperthermia (succinyl); histamine release
Antispasmodic agents
Zolpidem
Type: Benzodiazepines: Insomnia

Mechanism: Allosterically enhance binding of GABA

Use: Hypnotic - induces sleep

SE: Addictive; Drowsiness, ataxia, impaired judgment, tolerance
Benzodiazepines: Insomnia
Zaleplon
Type: Insomnia

Mechanism: Non-benzodiazepine

Use: Hypnotic - induces sleep

SE: Addictive; Drowsiness, ataxia, impaired judgment, tolerance
Insomnia
Phenobarbital
Type: Barbiturate: Insomnia and Anti-convulsant

Mechanism: Glutamate antagonist: inhibits reticular activating system

Use: Insomnia and anti-convulsant - epilepsy (long-acting)

SE: Sedation
Barbiturate: Insomnia and Anti-convulsant
Topiramate
Type: Anticonvulsant

Mechanism: Glutamate antagonist

Use: Secondary anti-epileptic drug

SE:
Anticonvulsant
Phenytoin
Type: Anticonvulsant; Anti-dysrhythmic

Mechanism: Inactivates Na channels

Use: Epilepsy; ventricular tachycardia

SE: Gingival hyperplasia, blur, vertigo, nystagmus
Anticonvulsant; Anti-dysrhythmic
L-Dopa (Levodopa)
Type: Parkinson's (Dopaminergic)

Mechanism: Increased DA synthesis: can cross BBB and becomes DA

Use: Parkinson's, Parkinsonism

SE: Dyskinesia; hallucinations; confusion
Parkinson's (Dopaminergic)
Carbidopa
Type: Parkinson's (Dopaminergic)

Mechanism: Dopa decarboxylase inhibitor

Use: Parkinson's, Parkinsonism

SE: Dyskinesia; hallucinations; confusion
Parkinson's (Dopaminergic)
Selegiline
Type: Parkinson's

Mechanism: Decreased DA catabolism: MAOB-I

Use: Parkinson's

SE:
Parkinson's
Bromocriptine
Type: Parkinson's

Mechanism: DA receptor agonists

Use: Use in combo with L-Dopa

SE: Parkinsonism
Parkinson's
Haloperidol
Type: Antipsychotics (Typical)

Mechanism: Dopamine antagonist

Use: Schizophrenia

SE: Sedation, dry mouth, sexual dysfunction, bradykinesis, tardive dyskinesia; Hyperprolactinemia; Moderate weight gain; neuroleptic malignant syndrome
Antipsychotics (Typical)
Risperidone
Type: Antipsychotics (Atypical)

Mechanism: Dopamine and serotonin antagonist

Use: Schizophrenia; mood stabilizer

SE: Sedation, dry mouth, sexual dysfunction, bradykinesis, tardive dyskinesia; Diabetes mellitus; Hypercholesterolemia; Hyperprolactinemia
Antipsychotics (Atypical)
Fluoxetine
Type: Antidepressants

Mechanism: SSRI

Use: First-line for depression; OCD; Bulimia; PMDD

SE: HA, tremor, insomnia; Serotonin syndrome: nervousness, shivers, confusion, sweating, fever, HTN, increased HR
Antidepressants (SSRIs)
Phenelzine
Type: Antidepressants

Mechanism: MAOI - Prevent breakdown of catecholamines; able to inhibit cytP450

Use: 2nd to 3rd-line anti-depressants

SE: Anti-muscarinic, anti-adrenergic; Hypotension, dry mouth, hypertensive crisis with tyramine; CNS excitation, suppression of REM sleep, hepatoxicity
Antidepressants (MAOI)
Bupropion
Type: Antidepressants (Atypical)

Mechanism:

Use: Also treats nicotine dependence

SE:
Antidepressants (Atypical)
Methimazole
Type: Antithyroid

Mechanism: Inhibits synthesis of thyroid hormone by accumulation

Use: Hyperthyroidism; prior to thyroid surgery or radiotherapy

SE: Hypothyroidism; arthralgia; pancytopenia
Antithyroid
Propylthiouracil
Type: Antithyroid

Mechanism: Interferes with use of iodine; blocks synthesis of T3 and T4

Use: Hyperthyroidism; iodine-induced thyrotoxicosis; thyroiditis; shrink thyroid before surgery

SE: HA, vertigo, loss of taste
Antithyroid
Potassium Iodide
Type: Antithyroid

Mechanism: Saturates the thyroid gland; inhibits hyperplastic thyroid gland

Use: Hyperthyroidism

SE: GI, irregular HR
Antithyroid
Somatostatin
Type: Antithyroid

Mechanism: Inhibits release of TSH and GH

Use: Hyperthyroidism

SE:
Antithyroid
Levothyroxine
Type: Thyroid

Mechanism: Synthetic form of thyroxine (T4): mimics activity of thyroid hormone; regulates basal metabolic rate

Use: Hypothyroidism

SE: Osteoporosis, arrhythmia
Thyroid
Insulin
Type: Hormone

Mechanism: Increases uptake of glucose

Use: Diabetes mellitus

SE:
Hormone
Chlorpropamide
Type: Diabetes: Sulfonylurea (1st gen)

Mechanism: Stimulate insulin release; inhibit glucose synth. from aa and FA; increase number of insulin receptors

Use: Mild to moderate DM2

SE: Hypoglycemia, blur, GI
Diabetes: Sulfonylurea (1st gen)
Glyburide
Type: Diabetes: Sulfonylurea (2nd gen)

Mechanism: Stimulate insulin release; inhibit glucose synth. from aa and FA; increase number of insulin receptors

Use: Mild to moderate DM2

SE: Hypoglycemia, blur, GI
Diabetes: Sulfonylurea (2nd gen)
Metformin
Type: Diabetes: Biguanide

Mechanism: promote glucose uptake by increasing insulin receptor binding; decrease gluconeogenesis; slow glucose absorption, increase glucose removal

Use: DM2 - keeps blood sugar levels from rising too high or too fast after meals

SE: Anorexia, GI
Diabetes: Biguanide
Pioglitazone
Type: Diabetes: Thiazolidinedione

Mechanism: Improves cells sensitivity to insulin by stim. of receptor in SkM, liver, and fat cells

Use: Adjuncts to diet for DM2

SE: hepatoxicity, edema, anemia
Diabetes: Thiazolidinedione
Acarbose
Type: Diabetes

Mechanism: Alpha-glucosidase inhibitor: inhibits absorption of sugar from GI

Use: DM2: Can be used in combo with Sulfonylurea

SE: GI, gas, hypoglycemia
Diabetes
Miglitol
Type: Diabetes

Mechanism: Alpha-glucosidase inhibitor: inhibits absorption of sugar from GI

Use: DM2: Can be used in combo with Sulfonylurea

SE: GI, gas, hypoglycemia
Diabetes
Pramlintide
Type: Diabetes

Mechanism: Inhibits glucagon

Use: DM2

SE:
Diabetes
Exenatide
Type: Diabetes

Mechanism: Inhibits glucagon

Use: DM2

SE:
Diabetes
Sitagliptin
Type: Diabetes

Mechanism: Inhibits glucagon

Use: DM2

SE:
Diabetes
Prednisone
Type: Corticosteroids

Mechanism: Anti-inflammatory

Use: Addison's disease, congenital adrenal hyperplasia; rheumatic, allergic, neoplastic, other; Topical: pruritis, psoriasis, eczema

SE: insomnia, behavioral changes, acute peptic ulcer; Cushing's, acne; osteoporosis, diabetes, delayed healing, cataracts, glaucoma
Corticosteroids
Ketoconazole
Type: Cushing's Disease

Mechanism: Biosynthetic inhibitor: decreases testosterone prod.

Use: Cushing's

SE:
Cushing's Disease
Mifepristone
Type: Cushing's Disease

Mechanism: Steroid receptor antagonist

Use: Cushing's

SE:
Cushing's Disease
Tamoxifen
Type: Non-steroidal Estrogen

Mechanism: Simulates estrogen

Use: Treatment and prevention of breast cancer

SE:
Non-steroidal Estrogen
Mifepristone
Type: Contragestational agent

Mechanism: anti-progestin

Use: contragestation

SE:
Contragestational agent
Methyltestosterone
Type: Androgen

Mechanism: Anabolic activity

Use: Correct hypogonadism, increase sperm prod, cryptorchidism, breast cancer, endometriosis, postpartem breast enlargement, fibrocystic breast disorder

SE: Insomnia, excitation, GI, increases libido
Androgen
Flutamide
Type: Androgen antagonist

Mechanism: antagonize androgen receptors

Use:

SE:
Androgen antagonist
Finasteride
Type: Anti-androgens

Mechanism: reduces prostate dihydrotestosterone

Use: benign prostatic hyperplasia - decreases prostate size

SE:
Anti-androgens
Verapamil
Type: Anti-HTN; Anti-Angina; Anti-dysrhythmic

Mechanism: Blocks Ca Channels

Use: Hypertension; slow heart rate, vasodilation, decreases vascular tone

SE: Dizziness; hypotension; HA
Anti-HTN; Anti-Angina; Anti-dysrhythmic
Phenoxybenzamine
Type: Anti-HTN

Mechanism: Peripherally acting: Inhibits NE release and storage

Use: Severe hypertension; decreases vascular tone and BP

SE: Drowsiness, HA
Anti-HTN
Losartan
Type: Anti-HTN

Mechanism: Angiotensin II receptor antagonist

Use: Hypertension; Blocks vasoconstriction and aldosterone secretion

SE: Cough, kidney damage, hyperkalemia
Anti-HTN
Captopril
Type: Anti-HTN

Mechanism: ACE Inhibitor: Stops converson of angiotensin I to angiotensin II

Use: Hypertension; vasodilation, increase renal blood flow

SE: Photosensitivity, kidney damage, hyperkalemia
Anti-HTN
Hydralazine
Type: Anti-HTN

Mechanism: Vasodilator

Use: Hypertension; increased blood flow and decreased BP; Must be used in combo with beta blockers and diuretics

SE: Tachycardia, HA, Hypotension
Anti-HTN
Hydrochlorothiazide
Type: Anti-HTN

Mechanism: Thiazide diuretic: promotes water loss; Works on convoluted tubule, collecting duct

Use: Mild to moderate Hypertension; edema; Decreases blood volume

SE: Hypokalemia, GI, jaudice
Anti-HTN
Furosemide
Type: Anti-HTN

Mechanism: Loop diuretic: promotes water loss; Works on loop of Henle

Use: Most potent - DOC for acute pulmonary edema (CHF), HTN, hypercalcemia (increases tubular Ca secretion)

SE: hyponatremia, hypokalemia, ototoxicity
Anti-HTN
Triamterene
Type: Anti-HTN

Mechanism: Potassium-sparing diuretic: Blocks epithelial sodium channel

Use: Hypertension; Mild diuresis w/o affecting blood K levels; edema

SE: Hyperkalemia
Anti-HTN
Aliskiren
Type: Anti-HTN

Mechanism: Renin inhibitor: inhibits conversion of angiotensinogen to angiotensin

Use: Hypertension; vasodilation

SE:
Anti-HTN
Cholestyramine
Type: Anti-Hyperlipidemia

Mechanism: Bile acid sequestrant: bind bile salts to form insoluble complex that is excreted

Use: Hyperlipidemia; decreases serum cholesterol and LDL

SE: Constipation, impaired absorption of fat-soluble vitamins
Anti-Hyperlipidemia
Clofibrate
Type: Anti-Hyperlipidemia

Mechanism: Fibric acid derivative: Blocks lipolysis of stored TG, inhibits uptake of Fas, inhibits prod of TG

Use: severe familial hypercholesterolemia

SE: GI, blurred vision, muscle weakness
Anti-Hyperlipidemia
Ezetimibe
Type: Anti-Hyperlipidemia:

Mechanism: Cholesterol Absorption blocker: Inhibits absorption of dietary lipid into intestinal tract

Use: Hyperlipidemia

SE:
Anti-Hyperlipidemia:
Orlistat
Type: Anti-Hyperlipidemia:

Mechanism: Cholesterol Absorption blocker: Inhibits lipase

Use: Hyperlipidemia

SE:
Anti-Hyperlipidemia:
Nicotinic Acid (Niacin)
Type: Anti-Hyperlipidemia

Mechanism: Decreases TG synthesis: lowers VLDLs, LDLs, and total cholesterol

Use: Hyperlipidemia; Adjuvant treatment

SE: Intense cutaneous flush, pruritis, gout
Anti-Hyperlipidemia
Warfarin
Type: Anticoagulant (Oral)

Mechanism: Interferes with hepatic synth of vit K-dependent clotting factors

Use: Long-term anticoagulant

SE: Bleeding, teratogenicity
Anticoagulant (Oral)
Heparin
Type: Anticoagulant (IV)

Mechanism: Inhibits conversion of prothrombin to thrombin and fibrinogen to fibrin

Use: Anticoagulant; Cardiovascular and lung disorders; open-heart surgery; dialysis

SE: Bleeding, fever, thrombocytopenia
Anticoagulant (IV)
Streptokinase
Type: Thrombolytic

Mechanism: Facilitate conversion of plasminogen to plasmin; hydrolyzes fibrin

Use: Dissolves blood clots; severe pulmonary embolism; DVT; arterial thromboembolism; MI, stroke

SE: Bleeding
Thrombolytic
Isosorbide Dinitrate
Type: Anti-angina: Nitrate

Mechanism: Dilate BV's; decrease cardiac oxygen demand; relaxes spasms; increase O2 supply

Use: Longer duration; all types of angina pectoris

SE: HA
Anti-angina: Nitrate
Propanolol
Type: Anti-dysrhythmic: Class II

Mechanism: Beta-Blocker

Use: Dysrhythmia - increases HR; heart excitability; conduction velocity; automaticity

SE: GI, insomnia, nightmares
Anti-dysrhythmic: Class II
Digoxin
Type: Ionotropic: Cardiac Glycoside

Mechanism: Inhibits sodium ATPase pump; increases intracellular Ca

Use: CHF; atrial fibrillation and flutter; decrease heart size, increase renal blood flow

SE: HA, visual disturbances
Ionotropic: Cardiac Glycoside
Ethacrynic acid
Type: Loop diuretics

Mechanism: Blocks reabsorption of Na, Cl, K, HCO3; (promotes water loss); Works on loop of Henle

Use: Most potent diuretics - DOC for acute pulmonary edema (CHF), HTN, hypercalcemia (increases tubular Ca secretion)

SE: hyponatremia, hypokalemia, ototoxicity
Loop diuretics
Furosemide
Type: Loop diuretics

Mechanism: Blocks reabsorption of Na, Cl, K, HCO3; (promotes water loss); Works on loop of Henle

Use: Most potent diuretics - DOC for acute pulmonary edema (CHF), HTN, hypercalcemia (increases tubular Ca secretion)

SE: hyponatremia, hypokalemia, ototoxicity
Loop diuretics
Ipecac
Type: Emetics

Mechanism: Irritates intestinal mucosal layer; stimulates vomiting center in medulla

Use: Induces vomiting

SE: Sedation
Emetics
Homatropine
Type: Cycloplegic mydriatic

Mechanism: Cholinergic antagonist

Use: Mydriasis and cycloplegia

SE:
Cycloplegic mydriatic
Scopolamine
Type: Cycloplegic mydriatic

Mechanism: Cholinergic antagonist

Use: Mydriasis and cycloplegia (also used as a preoperative drug)

SE:
Cycloplegic mydriatic
Cyclopentolate
Type: Cycloplegic mydriatic

Mechanism: Cholinergic antagonist

Use: Mydriasis and cycloplegia

SE:
Cycloplegic mydriatic
Tropicamide
Type: Cycloplegic mydriatic

Mechanism: Muscarinic antagonist

Use: Mydriasis and cycloplegia

SE:
Cycloplegic mydriatic
Epinephrine
Type: Mydriatic

Mechanism: Norepinephrine agonist

Use: Mydriasis

SE:
Mydriatic
Dapiprazole
Type: Miotic

Mechanism: Norepinephrine antagonist

Use: Miosis - used to reverse mydriasis

SE:
Miotic
Phentolamine
Type: Miotic

Mechanism: Norepinephrine antagonist

Use: Miosis

SE:
Miotic
Carbachol
Type: Miotic

Mechanism: Muscarinic agonist

Use: Miosis (used for glaucoma treatment)

SE:
Miotic
Pilocarpine
Type: Miotic

Mechanism: Muscarinic agonist

Use: Miosis (diagnostic for Adie's pupil)

SE:
Miotic
Echothiophate
Type: Miotic

Mechanism: Cholinesterase inhibitor

Use: Miosis

SE:
Miotic
Physostigmine
Type: Miotic

Mechanism: Cholinesterase inhibitor

Use: Miosis

SE:
Miotic
Benzalkonium chloride
Type: Preservative

Mechanism: Destroys or inhibits multiplication of microorganisms

Use: Inactive agent in topical drugs

SE: Epithelial toxicity with prolonged use
Preservative
Polyquaternium
Type: Preservative

Mechanism: Destroys or inhibits multiplication of microorganisms

Use: Inactive agent in topical drugs

SE: Epithelial toxicity with prolonged use
Preservative
Thimerosal
Type: Mercurial Preservative

Mechanism: Destroys or inhibits multiplication of microorganisms

Use: Inactive agent in topical drugs

SE: Epithelial toxicity with prolonged use
Mercurial Preservative
Purite
Type: Preservative

Mechanism: Destroys or inhibits multiplication of microorganisms

Use: Inactive agent in topical drugs

SE: Less toxic
Preservative
Gentamicin
Type: Topical Aminoglycosides

Mechanism: Bactericidal; concentration dependent; inhibits protein synthesis

Use: Effective against gram negatives

SE: Type IV delayed hypersensitivity reaction: low-grade blepharoconjunctivitis or blepharodermatitis; tobramycin has the least problems
Topical Aminoglycosides
Neomycin
Type: Topical Aminoglycosides

Mechanism: Inhibits protein synthesis

Use: Found only in combination formulation; cannot fight pseudomonas; Effective against gram negatives

SE: Type IV delayed hypersensitivity reaction: low-grade blepharoconjunctivitis or blepharodermatitis; tobramycin has the least problems
Topical Aminoglycosides
Tobramycin
Type: Topical Aminoglycosides

Mechanism: Bactericidal; concentration dependent; inhibits protein synthesis

Use: Effective against gram negatives; one of 4 most effective for adults

SE: Type IV delayed hypersensitivity reaction: low-grade blepharoconjunctivitis or blepharodermatitis; tobramycin has the least problems
Topical Aminoglycosides
Azithromycin
Type: Topical Macrolide

Mechanism: Time-dependent; interrupts protein synthesis

Use: High-viscosity solution; pediatric treatment

SE:
Topical Macrolide
Prednisolone (Pred Forte)
Type: Topical: Maximum strength steroid

Mechanism: Ketone-based - degraded slowly; enters cornea readily

Use: Greatest anti-inflammatory effect of all ophthalmic steroids; Uveitis; severe episcleritis; iritis; allergic conjunctivitis; Gold standard for post-operative inflammation control

SE: PSC and increased IOP
Topical: Maximum strength steroid
Loteprednol
Type: Topical: Maximum strength steroid

Mechanism: Ester-based - degraded more quickly than the rest

Use: Significant inflammatory conditions (Lotemax); taper use

SE: Minimized by shorter duration
Topical: Maximum strength steroid
Rimexolone
Type: Topical: Maximum strength steroid

Mechanism:

Use: FDA approved for post-operative inflammation control; anterior uveitis

SE: IOP-sparing effect
Topical: Maximum strength steroid
Fluorometholone alcohol
Type: Topical: Moderate strength steroid

Mechanism:

Use: Treats chronic inflammation (iridocyclitis, chronic allergy)

SE: IOP-sparing effect
Topical: Moderate strength steroid
Fluorometholone acetate
Type: Topical: Moderate strength steroid

Mechanism:

Use: More clinically effectice because of acetate

SE: IOP-sparing effect
Topical: Moderate strength steroid
Dexamethasone
Type: Topical: Low strength steroid

Mechanism:

Use: Less effective than prednisolone

SE: PSC and increased IOP
Topical: Low strength steroid
Trifluridine
Type: Topical Anti-viral

Mechanism:

Use: Herpes Simplex keratitis; use oral antiviral if ineffective

SE:
Topical Anti-viral
Diclofenac
Type: Topical NSAID

Mechanism: Anti-inflammatory

Use: Used for allergies

SE: Corneal toxicity, melting
Topical NSAID
Ketorolac
Type: Topical NSAID

Mechanism: Anti-inflammatory

Use: Used for allergies; also used for migraines

SE: Corneal toxicity, melting
Topical NSAID
Nepafenac
Type: Topical NSAID

Mechanism: prodrug - converts to amfenac (Can penetrate to posterior segment)

Use: post-cataract surgery inflammation (prevent cystoid macular edema)

SE: Corneal toxicity, melting
Topical NSAID
Bromfenac
Type: Topical NSAID

Mechanism: Enhanced ocular penetration

Use: Post-operative inflammation and pain

SE: Corneal toxicity, melting
Topical NSAID
Ketotifin
Type: Topical: Acute allergy

Mechanism: H1 receptor blocker

Use: Over the counter; both antihistamine and mast cell stabilization

SE:
Topical: Acute allergy
Olopatadine
Type: Topical: Acute allergy

(most popular)

Mechanism: H1 receptor blocker

Use: Both antihistamine and mast cell stabilization

SE:
Topical: Acute allergy
Epinastine
Type: Topical: Acute allergy

Mechanism: H1 receptor blocker

Use: Anti-histamine

SE:
Topical: Acute allergy
Azelastine
Type: Topical: Acute allergy

Mechanism: H1 receptor blocker

Use: Anti-histamine

SE:
Topical: Acute allergy
Brimonidine
Type: Alpha-2 agonist

Mechanism: Reduces IOP by 20% to 25%

Use: Glaucoma; used in addition to PG

SE: Ocular hyperemia
Alpha-2 agonist
Betaxolol
Type: Beta Blockers

Mechanism: Decreases production of aqueous humor

Use: Glaucoma; also used for HTN

SE:
Beta Blockers
Levobunolol
Type: Beta Blockers

Mechanism: Decreases production of aqueous humor

Use: Glaucoma

SE:
Beta Blockers
Timolol
Type: Beta Blockers

Mechanism: Reduction of aqueous humor production; reduces IOP by 25%

Use: Glaucoma; used in the morning

SE:
Beta Blockers
Acetazolamide
Type: CAI's

Mechanism: Inhibits carbonic anhydrase, and therefore production of aqueous humor

Use: Glaucoma

SE:
CAI's
Brinzolamide
Type: CAI's

Mechanism: Inhibits carbonic anhydrase, and therefore production of aqueous humor; reduces IOP by only 15%

Use: Glaucoma; ophthalmic suspension

SE:
CAI's
Dorzolamide
Type: CAI's

Mechanism: Inhibits carbonic anhydrase, and therefore production of aqueous humor; reduces IOP by only 15%

Use: Glaucoma; ophthalmic solution

SE:
CAI's
Latanoprost
Type: Prostaglandins

Mechanism: Increases uveoscleral flow; reduces IOP by 30%

Use: DOC for Glaucoma; used in the evening

SE: Hyperpigmentation; eyelash growth; conjunctival injection
Prostaglandins
Travoprost
Type: Prostaglandins

Mechanism: Increases uveoscleral flow; reduces IOP by 30%

Use: DOC for Glaucoma; used in the evening

SE: Hyperpigmentation; eyelash growth; conjunctival injection
Prostaglandins
Isosorbide
Type: Hyperosmotic agent

Mechanism: Creates an osmotic gradient that favors the movement of water out of body tissue

Use: Glaucoma - acute situations, not for chronic use

SE:
Hyperosmotic agent
Cephalexin
Type: Oral Antibiotic: penicillin

Mechanism: Inhibits cell wall growth

Use: Severe bacterial conjunctivitis

SE:
Oral Antibiotic: penicillin
Doxycylcine
Type: Oral Antibiotic: Tetracycline

Mechanism:

Use: Recurrent Corneal Erosion; prescribe with Lotemax; meibomian gland dysfunction

SE:
Oral Antibiotic: Tetracycline
Oral Prednisone
Type: Glucocorticoid

Mechanism: anti-inflammatory

Use: Marked or Stubborn Iridocyclitis; orbital pseudotumor; allergic blepharodermitis; Bell's Palsy

SE: Increases IOP
Glucocorticoid
Famcyclovir
Type: Oral Antivirals

Mechanism:

Use: Bell's Palsy

SE:
Oral Antivirals
Acyclovir
Type: Oral Antivirals

Mechanism:

Use: Herpes Simplex keratitis; use if trifluridine fails

SE:
Oral Antivirals
Clavulanic acid
Type: Antibiotic helper

Mechanism: Beta-lactamase inhibitor

Use: Used with amoxicillin to form Augmentin; common eye and eyelid infections

SE:
Antibiotic helper
Canthaxanthine
Type: Systemic Drug that causes eye problems

Mechanism:

Use: Oral suntanning agent, food and drug coloring agent

SE: Crystalline retinopathy
Systemic Drug that causes eye problems
Celecoxib
Type: Systemic Drug that causes eye problems

Mechanism: NSAID; COX-2 Inhibitor

Use: Inflammation

SE: Conjunctivitis; blurred vision
Systemic Drug that causes eye problems
Isotretinoin
Type: Systemic Drug that causes eye problems

Mechanism:

Use: Severe acne

SE: Lots of SE
Systemic Drug that causes eye problems
Sildenafil
Type: Systemic Drug that causes eye problems

Mechanism:

Use: ED (Viagra)

SE: Changes in color perception
Systemic Drug that causes eye problems
Alcohol
Type: Depressant

Mechanism:

Use: Recreational; treatment of methanol and ethylene glycol poisoning

SE: Fetal alcohol syndrome, altered drug metabolism, liver toxicity, GI, peptic ulcer, pacreatitis, cardiomyopathy, Wernicke-Korsakoff syndrome
Depressant
Disulfiram
Type: Aversive Pharmacotherapy

Mechanism: Produces acute sensitivity to alcohol

Use: Treats alcohol abuse

SE:
Aversive Pharmacotherapy
Naloxone
Type: Opioid Antagonist

Mechanism:

Use: Treats opioid dependence

SE:
Opioid Antagonist
Mescaline
Type: Psychedelic hallucinogen (phenethylamine class)

Mechanism: From peyote cactus - bind serotonin receptors

Use: Recreational

SE: Sympathetic NS activation
Psychedelic hallucinogen (phenethylamine class)
Marijuana
Type: Cannabinoid

Mechanism: Bind cannabinoid receptors (CB's), calcium and potassium ion channel activation

Use: Recreational, medicinal

SE:
Cannabinoid
PCP (Phencyclidine)
Type: Dissociative drug

Mechanism: NMDA receptor antagonist

Use: Formerly used as anesthetic agent; recreational

SE: Hallucinations; mania, delirium, disorientation, neurotoxicity
Dissociative drug
Aldosterone
Type: Hormone

Mechanism: Increases Na reabsorption; increases K secretion

Use: Regulates electrolytes

SE:
Hormone
Vasopressin
Type: Hormone

Mechanism: Makes the DCT and collecting duct permeable to water

Use: Water reabsorption - regulates water balance (increases BP and blood volume)

SE:
Hormone
Prolactin
Type: Hormone

Mechanism: Activates mammillary tissue

Use: Stimulates milk production

SE:
Hormone
Methanol
Type: Poison

Mechanism:

Use: Antidote: Ethanol; Gastric lavage, hemodialysis

SE: Retinal damage, decreased HR, respiratory depression
Poison