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132 Cards in this Set

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Tx for Acetaminophen OD
N-acetylcysteine
N-acetylcysteine is Tx for OD of
Acetaminophen
Tx for Salicylates
NaHCO3 (to alkalinize urine)
NaHCO3 would be Tx for OD of
Salicylates
Tx for OD of Amphetamines
NH4Cl (b/c amphetamines are basic)
NH4Cl would be Tx for this 'psych' drug
Amphetamines (b/c they're basic)
Tx for OD of AChE-I, Organophosphates
Atropine & Pralidoxime
(Pralidoxime regen's AChE)

Sx would be: DUMBBELSS: Diarrhea, Urination, Miosis, Bronchospasm, Bradycardia, Excitation of cns & muscle, Lacrimation, Salivation, Sweating
Atropine & Pralidoxime would be Tx for OD of
AChE-I or Organophosphate poisoning

Sx: DUMBBELSS: Diarrhea, Urination, Miosis, Bronchospasm, Bradycardia, Excitation of cns & muscle, Lacrimation, Sweating, Salivation

Pralidoxime regenerates active AChE
Tx for OD of Antimuscarinic or Anticholinergic agents
Physostigmine-salicylate
Physostigmine-salicylate would be Tx for OD of
Antimuscarinic or Anticholinergic agents
Tx for OD of beta-blockers & Verapamil
Glucagon, Ca, Atropine
Glucagon, Ca, Atropine are Tx for OD of
beta-blockers & Verapamil
Tx for OD of Digitalis
d/c Digitalis, normalize K, Lidocaine (if tachy), Mg, Atropine (if brady)
normalizing K, Lidocaine, & Mg are some of Tx for OD of _
Digitalis OD
also: d/c Dig, Atropine if brady, Lidocaine if tachy
Tx for OD of Iron
Deferoxamine

deFEroxamine (elemental symbol)
Deferoxamine is Tx for OD of
Iron
Tx of OD of Lead
Dimercaprol, Penicillamine, CaEDTA, Succimer

(Succimer for Kids, EDTA for adults)
Dimercaprol, Penicillamine, EDTA, Succimer are Tx for OD of
Lead

*Dimercaprol & Succimer also Tx for Hg, Arsenic, Gold
Tx for OD of Mercury, arsenic, gold
Dimercaprol, Succimer

*these are also part of Tx for OD of Lead
Tx of OD of Copper, arsenic, gold
Penicillamine

"Copper Peni's"
Cyanide OD Tx
Nitrites, hydroxycobalamin, thiosulfate

these oxidize Hg, binds CN, metabolite is excreted
Methemoglobin OD Tx
Methylene blue, Vit C, (Cimetidine can help too)
Methylene blue, Vit C are part of Tx of OD of
Methemoglobin
Carbon Monoxide OD Tx
100% O2, hyperbaric O2
Tx of OD of Methanol, Ethylene glycol
Fomepizol (best, since inhibits Alcohol-DH), Ethanol, Dialysis
Fomepizole, Ethanol, Dialysis are Tx for OD of
Methanol, Ethylene glycol
Tx of OD of Opiods
Naloxone/Naltrexone
Naloxone/Naltrexone are Tx for OD of
Opiods OD
Benzodiazepines OD is Tx'd w/
Flumazenil
Flumazenil is Tx for OD of
Benzodiazepines
OD of TCAs Tx
NaHCO3 (also for ASA OD)
Tx OD of Heparin w/
Protamine Sulfate
Protamine Sulfate is Tx for OD of
Heparin
Tx OD of Warfarin (Coumadin) w/
IV Vit K, FFP
IV Vit K & FFP is Tx for OD of
Warfarin (Coumadin)
Tx OD of tPA or Streptokinase w/
Aminocaproic Acid
Aminocaproic Acid is Tx for OD of
tPA or Streptokinase (thrombolytics)
Tx of OD of Theophylline is
beta-blocker
coronary vasospasm is common SE of
Cocaine
cutaneous flushing is common SE of (4)
Niacin, Dihydropyridine Ca-chnnl blockers (Nifidepine, Amlodipine, etc), Vancomycin, Adenosine
Dilated Cardiomyopathy is common SE of (2)
Doxorubicin, Dannorubicin
Torsades des pointes is common SE of (3)
Class I & III antiarrhythmics, Cisapride
Agranulocytosis is common SE of (6)
Clozapine, Carbamazepine, Colchicine, Propylthyouracil, Methimazole, Dapsone
Aplastic Anemia is common SE of (5)
Chloramphenicol, Benzene, NSAIDs, Propylthiouracil, Methimazole
Thrombocytopenia is common SE of (2)
Heparine, H2-blockers
Gray Baby Syndrome is common SE of
Chloramphenicol
Hemolysis in G6PD patients is common SE of (7)
INH, Sulfonamides, Primaquine, ASA, Ibuprofen, Nitrofurantoin, Dapsone, Chloroquine
Thrombosis is common SE of
OCPs, esp if smoking too
Pulmonary Fibrosis is common SE of
Bleomycin, Amiodarine, Busulfan
Cough is common SE of
ACE-I (give ARB in its place)
focal to massive hepatic necrosis is common SE of (3)
Halothane, Amiodarone, Busulfan
Hepatitis is common SE of
Macrolides
Pseudomembranous Colitis is common SE of (2)
Ampicillin, Clindamycin
Adrenocortical insufficiency is common SE of
glucocorticoid w/drawal
Gynecomastia is common SE of (7)
Spironolactone, Digitalis, Cimetidine, chronic Alcohol use, Ketoconazole, weed
Hot Flashes is common SE of (2)
Tamoxifen, Clomiphene
Hypothyroidism is common SE of (2)
Li, Amiodarone
Gingival hyperplasia is common SE of
Phenytoin
Gout is common SE of (2)
Furosemide, Thiazides
Osteoporosis is common SE of (2)
Corticosteroids, Heparin
Photosensitivity is common SE of (3)
Sulfonamides, Amiodarone, TET
Stevens-Johnson syndrome is common SE of (8)
"seizure, sulfa, 'scillins": Ethosuximide, Lamotrigine, Carbemazepine, Phenobarbital, Phenytoin, sulfa Rx's, PCN, Allopurinol
drug-induced SLE is common SE of (5)
SHIPP!!!: Sulfonamides, Hydralazine, Isoniazid, Phenytoin, Procainamide
Tendon rupture/cartilage damage is common SE of
Fluoroquinolones
Fanconi's syndrome is common SE of (3)
expired TET's, heavy metals, Wilson's
Interstitial nephritis is common SE of (3)
NSAIDs, Methicillin, Furosemide
Hemorrhagic Cystitis is common SE of (2)
Cyclophosphamide (Tx w/ MESNA), Furosemide
dizziness, N, HA, vision changes, tinnitus are common SE of (3)
Quinidine, Quinine (& Digitalis)
Nephrogenic DI is common SE of (2)
Li, Democlocycline
Seizure is common SE of (5)
Enflurane, Buproprion, Imipenem/Cisplatin, Isoniazid, evening Palm Rose Oil
Tardive Dyskinesia is common SE of
high potency anti-psychotics
Disulfiram-like rxn is common SE of
Metronidazole
Nephro + Neurotoxicity is common SE of
Polymyxins
Nephro + Ototoxicity is common SE of
Aminoglycosides, Vancomyocin, Loop Diuretics, Cisplatin
skin disorder w/:
pruritic, purple, polygonal papules
Lichens Planus

-sawtooth infiltrate at dermal-epidermal junction
skin disorder w/:
life threatening rash w/ bulla
Stevens-Johnson syndrome

-fever, bulla formation & necrosis, sloughing of skin
skin disorder w/:
pruritis a/w asthma
Atopic Dermatitis (Eczema)

pruritic eruption, esp on skin flexures
skin disorder w/:
pruritic vesicles a/w celiac disease
Dermatitis Herpetiformis

deposits of IgA at tips of Dermal Papillae
skin disorder w/:
allergy to nickel
Type IV (contact dermatitis)
skin disorder w/:
thickened scar esp around face/chest
Keloid
skin disorder w/:
Ab against Epidermal Basement Membrane
Bullous Pemphigoid

-Ab to Hemidesmosomes
Bullous pemphigoid = Basement membrane "B!"
-(-) Nikolsky's sign, SPARES Oral mucosa
skin disorder w/:
tense blisters, oral mucosa spared, Ab to basement membrane
Bullous Pemphigoid
skin disorder w/:
Ab against Epidermal cell junctions
Pemphigus Vulgaris

-Pemphigus Vulgaris = Positive nikolsky's sign = skin sloughs off w/ stroking
-Ab to Desmosomes
-affects Oral mucosa
skin disorder w/:
parakeratotic scaling
Psoriasis

-papules & plaques w/ *silvery scaling*, acanthosis w/ *parakeratotic scaling*
-incr Stratum Spinosum, decr Stratum Granulosum
skin disorder w/:
keratin-filled cysts
Seborrheic Keratosis

-flat, greasy, pigmented prolif that looks 'pasted on'
skin disorder w/:
sand-paper; predisposition to SCC
Actinic Keratosis
skin disorder w/:
skin rash & proximal muscle weakness
Dermatomyositis
skin disorder w/:
honey-colored lesions common on nose & lips
Impetigo

S aureus or S pyogenes
skin disorder w/:
hyperkeratosis & koilocytosis
Verrucase of HPV
skin disorder w/:
histology shows palisading nuclei
Basal Cell Carcinoma

-sun-exposed areas
-mets = rare
-rolled edges w/ central ulceration
skin disorder w/:
ulcerative red lesion in sun-exposed area, histo: Keratin "Pearls"
Squamous Cell Carcinoma

-mets = rare
skin disorder w/:
S-100, sun exposure, dark w/ irregular borders
Melanoma

-mets = common
-depth correlates w/ risk of mets
enzyme deficient in lysosomal storage disease w/ renal & cardiovascular manifestations
Fabry's disease
-enzyme defic = α-galactosidase A
-Fabry's fucks w/ the kidneys
-only Fabry's & Hunter's are X Recessive (all others = AR)
-other Sx: periph neuropathy of hands/feet, angiokeratomas
the only 2 X-linked lysosomal storage diseases, & what enzyme defic in them?
only 2 X-linked are Fabry's & Hunter's
Fabry's = no α-galactosidase A; Hunter's = no Iduonate sulfatase (accum Heparan sulfate & Dermatan sulfate)
enzyme defic in the m/c lysosomal storage disease?
β-glucocerebrosidase
-defic in Gaucher's

-accumulate Glucocerebroside
-hepatosplenomegaly, aseptic necrosis of femur, macrophages that look like "crumpled tissue paper" = Gaucher cells
which lysosomal storage diseases a/w early death (& their enzymes)
Tay-Sach's, Niemann-Pick, Krabbe's

Tay-Sach's = tay-saX = heXosaminidase A

Nieman-Pick = Sphinogomyelinase
"Niemann Picks his nose w/ his Sphinger"

Krabbe's = Galactocerebrosidase
which lysosomal storage disease(s) is(are) demyelinating and defic enzyme(s)
Metachromatic Leukodystrophy

-defic in Arylsulfatase A
-Sx: central & peripheral demyelination w/ ataxia, dementia
of the following, which has Corneal Clouding, which has Mental Retardation

Hurler's

Hunter's

Scheie's

I-cell
Hurler's: Corneal Clouding, Mental Retardation

Hunter's: only Mental Retardation

Scheie's: only Corneal Clouding

I-cell: Corneal Clouding, ~Mental Retardation
α-L-iduronidase is defic in
Hurler's Syndrome (lysosomal storage diseaes)

-Schei's is a milder version of this
Iduronate sulfatase is defic in
Hunter's Syndrome (lysosomal storage disease)

-X-linked recessive (Fabry's is the only other XR lysosomal storage defect, all others are AR)
Arylsulfatase A is defic in
Metachromatic Leukodystrophy

-central & peripheral demyelination w/ ataxia & dementia
α-galactosidase is defic in
Fabry's disease (lysosomal storage disease)

-X-linked recessive (only this and Hunter's are, all others AR)
Galactocerebrosidase is defic in
Krabbe's disease (lysosomal storage disease)

Sx: periph neuropathy, developmental delay, optic atrophy
β-glucocerebrosidase is defic in
Gaucher's disease (lysosomal storage)

Sx: hepatosplenomegaly, femur aseptic necrosis, crumpled tissue paper macrophages (Gaucher's cells)
Hexosaminidase is defic in
Tay-Sach's (lysosomal storage disease)

"tay-saX"
Sx: neurodegen, developmental delay, cherry-red spot on macula, NO hepatosplenomegaly (vs Nieman-Pick, DOES have hepatosplenomegaly)
Sphingomyelinase defic in
Nieman-Pick (lysosomal storage disease)
GM2-ganglioside accumulates in
Tay-Sach's
-defic Hexosaminidase A

-NO hepatomegaly, cherry-red spot on macula
Dermatan sulfate accumulates in
Hunter's & Hurler's syndromes (lysosomal storage diseases)

Hurler's: development delay, Gargoylism, airway obstruction, corneal clouding, dwarfism, hepatosplenomegaly

Hunter's: mild Hurler's, aggresive behavior, NO corneal clouding
lysosomal storage disease common in Ashkenazi Jew's
Tay-Sach's, Niemann-Pick, Gaucher's
lysosomal storage disease w/ "crinkled paper cytoplasm"
Gaucher's disease (the m/c)
cherry red spot on macula DDx
Niemann-Pick
Tay-Sach's
Central Retinal a occlusion
how differentiate btw Niemann-Pick & Tay-Sachs
-BOTH have neurodegeneration, developmental delay, **Cherry Red spot on macula**

Niemann-Pick: progressive neurodegeneration, hepatosplenomegaly, cherry-red spot, foam cells (macropages), retardation

Tay-Sach's has NO hepatomegaly
"no SACH in the liver"
enzyme defic if pt w/ cherry-red spot on macula, hepatomegaly, retardation
Sphingomyelinase

-this is Niemann-Pick

(vs Tay-Sach's also has retardation & cherry-red spot on macula, but NO hepatomegaly, and is Hexosaminidase A)
what vasculitis fits description:
weak pulses in UE
Takayasu's arteritis

-"pulseless disease"
-giant cell granulomatous thickening or aortic arch &/or proximal great vessels
-can have BP diff in R vs L extremity
Sx: Fever, Arthritis, Night sweats, MYalgia, SKIN nodules, Ocular disturb's, Weak pulses in UE, UE can have discrepancy
what vasculitis fits description:
necrotizing granulomas of lung & necrotizing glomerulonephritis
Wegener's Granulomatosis

-focal necrotizing vasculitis, necrotizing granulomas in Lung AND Upper Airway, necrotizing glomerulonephritis (the airway thing differentiates from Goodpasture's)
Sx: hemoptysis, hematuria, perforation of nasal septum, chronic sinusitis, otitis media, mastoiditis, cough
******c-ANCA(+)*****
what vasculitis fits description:
young male smokers
Buerger's
-"thromboangiitis obliterans", idiopathic, segmental thrombosing vasculitis
Sx: intermittent claudication, superficial nodular phlebitis, Raynaud's, gangrene & autoamputation
what vasculitis fits description:
young Asian women
Takayasu's Arteritis

-Asian F < 40 y.o, giant cell granulomatous thickening of aortic arch &/or proximal great vessels
Sx: Fever, Arthritis, Night sweats, MYalgia, SKIN nodules, Ocular distrub's, Weak pulses in UE w/ discrepancy btw the UE
"FAN MY SKIN On Wed"
what vasculitis fits description:
young asthmatics
Churg-Strauss Syndrome

-granulomatous vasculitis w/ eosinophilia; m/c presents w/ Asthma, Sinusitis, Skin Lesions, Peripheral Neuropathy

Vasculitis, young asthmatic- Churg-Strauss
what vasculitis fits description:
infants & young children, involves coronary arteries
Kawasaki's Disease

-acute, self-limiting necrotizing vasculitis in infants/kids; a/w Asian race
-Sx: fever, conjunctivitis, lip/oral mucosal changes ("strawberry tongue"), lymphadenitis, desquamative skin rash
*coronary a aneurysm*
Tx: IV Ig, ASA (***this is the rare instance when give a child ASA***)
what vasculitis fits description:
m/c vasculitis
Temporal Arteritis

-focal, granulomatous inflamm, esp in eldery F
Sx: unilateral HA, jaw claudication, impaired vision
*ophthalmic a is occluded, can → irreversible blindness
what vasculitis fits description:
a/w Hep B infection
Polyarteritis Nodosa

-immune-complex med'd transmural vasculitis w/ fibrinoid necrosis
Sx: fever, wt loss, malaise, abd pain, melena, HA, myalgia, HTN, neurologic dysfunction, cutaneous eruptions
what vasculitis fits description:
occlusion of ophthalmic a possibly causing blindness
Temporal Arteritis

-focal, granulomatous inflamm
what vasculitis fits description:
perforation of nasal septum
Wegener's

triad of: focal necrotizing vasculitis, necrotizing granulomas in lung AND upper airway (Goodpasture's is just lung), necrotizing glomerulonephritis
Sx: hemoptysis, hematuria, nasal septum perforation, chronic sinusitis, otitis media, mastoiditis, cough, dyspnea
*****c-ANCA*****
what vasculitis fits description:
unilateral HA, jaw claudication
Temporal Arteritis
skin papule in AIDS caused by Bartonella is a/w which vascular tumor
Bacillary Angiomatosis
cavernous lymphangioma a/w Turner's syndrome is a/w what vascular tumor
Cystic Hygroma
which vascular tumor is a/w benign red lesion about size of mole in elderly
Cherry Hemangioma
which vascular tumor is a/w raised, red area present at birth, incr's size initially, then regresses over mo to years
Strawberry Hemangioma
which vascular tumor is a/w lesion caused by lymphoangiogenic growth factors in an infected HIV pt
Kaposi's sarcoma
vascular tumor a/w polypoid red lesion found in pregnancy or after trauma
Pyogenic granuloma
vascular tumor a/w benign, painful, red-blue tumor under fingernails
Glomus Tumor
vascular tumor a/w cavernous lymphangioma a/w Turner's
Cystic Hygroma