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
|