AEs Flashcards

1
Q

Beta-lactams

A

Hypersensitivity reactions

Seizures (high doses)

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2
Q

Natural PCNs

A

Normal beta-lactam AEs

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3
Q

Anti-staphylococcal PCNs

A

Normal beta-lactam AEs
Interstitial nephritis
Phlebitis

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4
Q

Aminopenicillins

A

Normal beta-lactam AEs

Diarrhea w/PO (more common with ampicillin than amoxicillin b/c amox. is better absorbed)

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5
Q

Antipseudomonal PCNs

A

Normal beta-lactam AEs

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6
Q

Beta-lactam/Beta-lactamase inhibitor combinations

A

Normal beta-lactam AEs

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7
Q

1st Generation Cephalosporins

A

Normal beta-lactam AEs

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8
Q

2nd Generation Cephalosporins

A

Normal beta-lactam AEs

Cefotetan can inhibit Vit K production and prolong bleeding; can also cause disulfuram-like rxn when given with ethanol

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9
Q

3rd Generation Cephalosporins

A

Normal beta-lactam AEs

Ceftriaxone can lead to biliary sludging and hyperbilirubinemia in neonates; best to use cefotaxime instead

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10
Q

4th Generation Cephalosporins

A

Normal beta-lactam AEs

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11
Q

Anti-MRSA Cephalosporins

A

Normal beta-lactam AEs

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12
Q

Cephalosporins/Beta-lactamase inhibitors

A

Normal beta-lactam AEs

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13
Q

Carbapenems

A

Normal beta-lactam AEs
Increased risk of seizures; esp w/imipenem; minimize risk by using appropriate adj. and avoid imipenem in patients with CNS infxns (d/t ability to cross BBB more readily)

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14
Q

Monobactams

A

Normal beta-lactam AEs

Low incidence of hypersensitivity

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15
Q

Fluoroquinolones

A

CNS (dizziness, confusion, hallucinations, peripheral neuropathy, insomnia)
CV (QT prolongation)
Musculoskeletal (arthralgies [common], achilles tendon rupture [BBW: very rare, more likely in the elderly, renal dysfunction, and patients on corticosteroids])
Dermatologic (photosensitivity)
Developmental (contraindicated in pregnancy and children [cartilage lesions seen in juvenile beagle dogs])

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16
Q

Macrolides and Ketolides

A

GI: worst with erythromycin (it is used as a prokinetic agent for patients with impaired GI motility)
Hepatic: rare but serious (recent reports with telithromycin-induced hepatic failure leading to transplantation and death)
CV: Increased QT interval (use with caution in patients with pre-existing heart conditions, those on anti-arrhythmics, or taking interacting drugs)

17
Q

Aminoglycosides

A

Nephrotoxicity: dose-related, risk higher with higher trough concentrations
Ototoxicity: dose-related, risk higher with high peak concentrations and long-term use (> 2 weeks)
Neuromuscular blockade: can occur, esp. in higher doses in patients who are also receiving paralytic agents

18
Q

Vanc.

A

Ototoxicity/nephrotoxicity have classically been assigned to vanc.
Nephrotoxicity may occur at high doses. The early formulation was brown ad dubbed “Mississippi mud.” The current formulation is clear and lacks those toxic excipients
“Red-Man Syndrome” (pt feels warm, flushed, and can be hypotensive. Can be prevented by slowing the infusion rate or adding antihistamines prior to infusion. Not a true allergy)

19
Q

Telavancin

A
Renal toxicity
Taste disturbances
Foamy urine
Red Man syndrome
QT prolongation
AVOID pregnancy
20
Q

Dalbavancin

A
Infusion reactions
AST elevations
Nausea
H/A
Diarrhea
21
Q

Oritavancin

A
Increases warfarin exposure
Can falsely prolong aPTT for up to 48 hours and PT/INR for up to 24 hours
Infusion reactions
H/A
N/V/D
Limb and SQ abscessess
22
Q

Cyclic Lipopeptides

A

Muscle pain or weakness
Possibly rhabdomyolysis
Creatine Kinase concentrations should be checked weekly while on therapy

23
Q

Linezolid

A

Can cause bone marrow suppression (esp. thrombocytopenia) with long term therapy (> 2 weeks)
Can cause peripheral neuropathy, lactic acidosis with long term therapy d/t toxicity to mitochondria

24
Q

Tedizolid

A

N/V/D

H/A

25
Q

Streptogramins

A

Phlebitis; should be administered as a central line, if possible
High incidence of myalgias and arthralgias

26
Q

Tetracyclines and glycylcyclines

A
GI
Photosensitivity
Esophageal irritation
Discoloration of developing teeth
Contraindicated in pregnant women and children < 8yr
27
Q

Nitroimidazoles

A

GI: N/V/D, metallic taste is common. Hepatitis and pancreatitis are rare.
Neuro: dose-related, reversible peripheral neuropathy reported occasionally

28
Q

Lincosamides

A

DIARRHEA!!! Can cause self-limiting diarrhea or can result in more severe diarrhea resulting from superinfection with C. difficile.
C. difficile associated diarrhea and colitis can occur during or after clindamycin therapy and can be life-threatening. Pts with diarrhea need evaluation for C. difficile disease, especially if it is severe, associated with fever, or persists after the end of clindamycin therapy

29
Q

Nitrofurans and Fosfomycin

A

GI: N/V

Peripheral neuropathy may also occur

30
Q

Nitrofurantoin and pulmonary toxicity

A

Can cause very rare but serious pulmonary toxicity of forms. First is an acute pneumonitis manifesting as cough, fever, and dyspnea. This form typically revolves soon after drug d/c. A chronic pulmonary fibrosis can occur, most commonly with prolonged therapy duration; recovery of lung function is limited after drug d/c.

31
Q

Folate antagonists

A

Dermatologic (RASH** most common, life-threatening rxns such as toxic epidermal necrolysis and Stevens-Johnson syndrome have been documented)
Hematologic (dose-dependent bone marrow suppression)
Renal (Can cause true and pseudo-renal failure. Crystalluria and acute interstitial nephritis due to the SMX component can lead to acute renal failure; however, the blockade of creatinine secretion by TMP can cause an increase in serum creatinine w/out a true decline in GFR. TMP can also cause hyperkalemia)

32
Q

Fidaxomicin

A

GI: N/V/D, abdominal pain, GI hemorrhage, anemia, neutropenia