About the Author
Jennifer Gershman, PharmD, CPh, PACS, is a drug information pharmacist and Pharmacy Times contributor who resides in South Florida.
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Pharmacists can counsel patients and educate the health care team about the risks of pharmacologically caused illnesses.
Medications can be lifesaving and vital for managing chronic diseases, but it is important to keep in mind that medications can also be associated with drug-induced diseases. These are defined as an unintended drug effect that results in morbidity and mortality.1 Symptoms result in the patient seeking emergency attention and/or requiring hospitalization.1,2 Postmarketing surveillance is critical to identifying drug-induced diseases, and pharmacists play a vital role in identifying and managing drug-induced diseases.3-7
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There are a variety of medications that can result in drug-induced diseases. Fluoroquinolone antibiotics, such as ciprofloxacin and levofloxacin, are one example.2 The FDA added a boxed warning to fluoroquinolones in 2008 about the increased risk of tendinitis and tendon rupture. Additionally, myasthenia gravis symptom exacerbation was added to the boxed warning.2
Jennifer Gershman, PharmD, CPh, PACS, is a drug information pharmacist and Pharmacy Times contributor who resides in South Florida.
In 2018, the FDA issued a drug safety communication about strengthening the labeling warnings section of fluoroquinolones regarding the risks of hypoglycemia and mental health adverse effects, including agitation, nervousness, memory impairment, and delirium.2 Because fluoroquinolones are associated with many drug-induced diseases, they should be reserved for serious bacterial infections, such as pneumonia. Fluoroquinolones can be considered if first-line agents fail to treat bacterial sinusitis, chronic bronchitis, and uncomplicated bacterial infections.
Pharmacists can play an important role in preventing and identifying fluoroquinolone drug–induced diseases. Recommending alternative antibiotics and reporting adverse effects to the FDA’s MedWatch program are a couple of examples. Reporting adverse drug reactions assists with the postmarketing surveillance process for medications.
In some cases, drug interactions can contribute to drug-induced diseases. For instance, the use of proton pump inhibitors (PPIs) with clopidogrel (Plavix; Sanofi) can lower the risk of gastrointestinal adverse effects.3 However, PPIs may reduce the efficacy of clopidogrel, causing an increased risk of cardiovascular adverse events, such as myocardial infarction and stroke.3 Omeprazole (Prilosec; AstraZeneca) has been found to be the most likely PPI to cause this interaction with clopidogrel.
Additionally, long-term use of PPIs can increase the risk of developing osteoporosis.4 Approximately 25% to 70% of PPI prescriptions do not have an appropriate indication.5 Additionally, PPIs can cause a variety of other drug-induced diseases, including Clostridioides difficile, dementia, pneumonia, and nutrient deficiencies.5 Studies have shown that pneumonia may occur within the first month of starting a PPI,5 whereas other research shows that hypomagnesemia can occur within 3 months of starting a PPI; however, in most cases, it tends to happen after 1 year of PPI use.5 This prompted the FDA to issue a drug safety communication in 2011 about the link between PPIs and hypomagnesemia.6
Pharmacists can educate patients about the link between long-term PPI use with drug-induced diseases during medication therapy management consults. Additionally, pharmacists can assist with deprescribing PPIs that are no longer needed or are being used for inappropriate indications.7 This is especially critical in patients who develop or are at risk for adverse events. It is also important to educate patients that OTC PPIs should not be used for more than 14 days at a time every 4 months.6