General information

Clarithromycin is a commonly used macrolide antibiotic and is a regular part of regimens for the eradication of Helicobacter pylori , often in combination with a nitroimidazole antibiotic as well, in addition to a proton pump inhibitor. Variable rates of adverse events (4–30%) have been reported with clarithromycin.

The most common adverse reactions to clarithromycin in clinical trials were diarrhea and abnormal taste, both of which occurred in 6% of patients [ ]. Other events that occurred less often were nausea (3%), dyspepsia (2%), abdominal pain (2%), and headache (2%). Clarithromycin can also cause fixed drug eruptions, hypersensitivity reactions, and leukocytoclastic vasculitis. It can also cause mania, especially when given with glucocorticoids.

Drug studies

Comparative studies

In a double-blind, multicenter trial in 328 patients with H . pylori infection and non-ulcer dyspepsia, omeprazole 20 mg bd, amoxicillin 1 g bd, and clarithromycin 500 mg bd were compared with omeprazole alone. The rate of success and quality of life were similar in both groups. There were no serious adverse events. However, there were 12 withdrawals in the group given omeprazole and antibiotics and two in the group given omeprazole alone. Diarrhea occurred in 63 patients in those given omeprazole and antibiotics and in 10 patients given omeprazole alone [ ]. In another double-blind, placebo-controlled trial eradication of H . pylori (omeprazole 20 mg, amoxicillin 1 g, and clarithromycin 500 mg bd) in long-term users of NSAIDs with past or current peptic ulcer or troublesome dyspepsia led to impaired healing of gastric ulcers and did not affect the rate of peptic ulcers or dyspepsia over 6 months [ ].

Clarithromycin versus beta-lactam antibiotics

In a multicenter, double-blind, randomized comparison of cefprozil, 500 mg bd for 5 days and clarithromycin 500 mg bd for 10 days in 295 subjects with an acute exacerbation of chronic bronchitis, the most common adverse effects of clarithromycin were nausea (8%), diarrhea (12%), taste disturbance (8%), and dry mouth (5%) [ ].

Clarithromycin (250 mg bd for 10 days) was as effective as cefuroxime axetil (250 mg bd for 10 days) in the treatment of acute maxillary sinusitis in a randomized, double-blind, multicenter study in 370 patients; 10% of patients in each group had adverse events [ ].

Clarithromycin versus other macrolides

The incidence of disseminated Mycobacterium avium complex (MAC) infection has increased dramatically with the AIDS epidemic. Treatment regimens for patients with a positive culture for MAC from a sterile site should include two or more drugs, including clarithromycin. Prophylaxis against disseminated MAC should be considered for patients with a CD4 cell count of less than 50 × 106/l [ ]. In a randomized, open trial in 37 patients with HIV-associated disseminated MAC infection, treatment with clarithromycin + ethambutol produced more rapid resolution of bacteremia, and was more effective at sterilization of blood cultures after 16 weeks than azithromycin + ethambutol [ ].

In a direct comparison of clarithromycin with erythromycin stearate, the rate of adverse events was 19% in 96 patients taking clarithromycin and 35% in 112 patients taking erythromycin [ ]. Most of the adverse events associated with clarithromycin affect the gastrointestinal tract (7%).

In a prospective, single-blind, randomized study of a 7-day course of clarithromycin (7.5 mg/kg bd) and a 14-day course of erythromycin (13.3 mg/kg tds) in 153 children with pertussis, the incidence of treatment-emergent drug-related adverse events was significantly higher with erythromycin than with clarithromycin (62% versus 45%) [ ]. Three subjects given erythromycin withdrew prematurely because of adverse events: one because of a rash; one with vomiting and diarrhea; and one with vomiting, abdominal pain, and rash.

Clarithromycin versus fluoroquinolones

In a multicenter, double-blind, randomized comparison of trovafloxacin 200 mg and clarithromycin 500 mg bd in 176 subjects with acute exacerbations of chronic bronchitis, the most common adverse effects of clarithromycin were nausea (3%), diarrhea (4%), and taste disturbances (4%) [ ].

Clarithromycin versus tetracyclines

Clarithromycin (0.75–2 g/day), minocycline (200 mg/day), and clofazimine (100 mg/day) for 15 months were investigated as treatment of MAC lung disease in 30 HIV-negative patients. Eight patients did not complete the study owing to deviations from protocol or adverse effects. Persistently negative cultures were found in 14 of the other patients. There were three cases of hepatic disturbances and three of ototoxicity, which required a reduction in clarithromycin dosage after a short interruption of treatment [ ].

Organs and systems

Cardiovascular

Clarithromycin caused modest but significant prolongation of the QT c interval in 28 children with respiratory tract infections after 24 hours of treatment (mean prolongation 22 ms; 95% CI = 14, 30); in seven cases the QT c interval was over 440 ms, and in one case it was over 460 ms [ ].

  • QT interval prolongation and a ventricular dysrhythmia occurred in an HIV-positive 30-year-old man at the start of intravenous clarithromycin therapy 500 mg 12-hourly [ ].

Intravenous clarithromycin caused thrombophlebitis in four patients when it was given inappropriately as a rapid bolus injection instead of a short infusion; the manufacturers have received other reports of similar reactions, even with infusions, but the incidence seems to be considerably lower than with erythromycin [ ]. In a prospective, non-randomized study, phlebitis occurred in 15 of 19 patients treated with intravenous erythromycin (incidence rate of 0.40 episodes/patient-day) and in 19 of 25 patients treated with intravenous clarithromycin (0.35 episodes/patient-day) [ ].

Respiratory

Bronchospasm with clarithromycin occurred in a 44-year-old woman who had no history of respiratory allergies but had had adverse drug reactions to general and regional anesthetics and to ceftriaxone [ ]. After the administration of a quarter of the therapeutic dose the patient had dyspnea, cough, and bronchospasm throughout the lung.

Pulmonary infiltration with eosinophilia occurred in a 17-year old youth who took clarithromycin 500 mg bd for 7 days; clarithromycin was immediately withdrawn, and he quickly recovered [ ].

Nervous system

Adverse events on the nervous system due to clarithromycin have been observed in 3% of patients.

  • Progressive loss of strength and difficulty in swallowing and eye opening after the first dose of clarithromycin (2 g/day) occurred in a patient with cerebral toxoplasmosis and AIDS [ ]. This myasthenic syndrome resolved within 6 hours of withdrawal of clarithromycin and administration of pyridostigmine.

The authors postulated that this adverse effect may have been the consequence of neuromuscular blockade, through inhibition of the presynaptic release of acetylcholine.

Sensory systems

Eyes

Topical clarithromycin can cause self-resolving corneal deposits [ ].

Hearing

Tinnitus has been attributed to clarithromycin.

  • A 50-year-old man developed tinnitus 9 days after he started to take clarithromycin 500 mg bd for a peptic ulcer [ ]. The clarithromycin was withdrawn, but the patient continued to take his other medications (amoxicillin, and lansoprazole). The tinnitus resolved after 2 days and he did not have any other symptoms.

  • An 81-year-old woman developed irreversible sensorineural hearing loss in the right ear 3 days after starting low-dose clarithromycin for an acute exacerbation of chronic obstructive pulmonary disease [ ].

  • Ototoxicity was attributed to clarithromycin in a 76-year-old man 4 days after he started to take clarithromycin for atypical pulmonary tuberculosis [ ]. When the clarithromycin was withdrawn his hearing improved subjectively, but it worsened again on re-exposure.

Taste

Abnormal taste developed in 17 of 175 patients treated with clarithromycin 250 mg bd for 10 days for community-acquired pneumonia, compared with 3 of 167 patients treated with sparfloxacin [ ]. Mild to moderate gastrointestinal disturbances were the most common adverse events and were reported in 13 and 11% respectively.

Psychiatric

Two patients, a man aged 74 and a woman aged 56 years, developed delirium after taking clarithromycin [ ].

  • A 63-year-old woman took clarithromycin for a community-acquired pneumonia and had an episode of agitation and delirium; she recovered when the clarithromycin was stopped [ ].

  • Two patients (aged 21 and 33 years) with late-stage AIDS had acute psychoses shortly after taking clarithromycin (2 g/day) for MAC bacteremia [ ]. In both cases the psychosis resolved on withdrawal but recurred on rechallenge. In one case treatment with azithromycin was well tolerated.

Of cases of mania attributed to antibiotics and reported to the WHO, 28% were due to clarithromycin [ ].

  • A 77-year-old man who was HIV-negative developed mania after 6 days treatment with clarithromycin 1 g/day for a soft tissue infection; his mental state resolved on withdrawal [ ].

  • A 53-year-old Canadian lawyer taking long-term fluoxetine and nitrazepam developed a frank psychosis 1–3 days after starting to take clarithromycin 500 mg/day for a chest infection [ ]. His symptoms resolved on withdrawal of all three drugs, and did not recur with erythromycin or when fluoxetine and nitrazepam were restarted in the absence of antibiotics.

The symptoms may have been due to a direct effect of clarithromycin or else inhibition of hepatic cytochrome P450 metabolism, leading to fluoxetine toxicity.

Clarithromycin occasionally causes hallucinations.

  • Visual hallucinations with marked anxiety and nervousness occurred after the second dose of oral clarithromycin 500 mg in a 32-year-old woman [ ]. Clarithromycin was withdrawn and the symptoms disappeared a few hours later.

  • Visual hallucinations developed in a 56-year-old man with chronic renal insufficiency and underlying aluminium intoxication maintained on peritoneal dialysis 24 hours after he started to take clarithromycin 500 mg bd for a chest infection, and resolved completely 3 days after withdrawal [ ].

Hematologic

  • Thrombotic thrombocytopenic purpura was reported in a 42-year-old man with no past medical history after he had just completed a 30-day course of clarithromycin 250 mg bd [ ].

Gastrointestinal

Erythromycin acts as a motilin receptor agonist [ ]. This mechanism may be at least partly responsible for the gastrointestinal adverse effects of macrolides. Clarithromycin may act on gastrointestinal motility in a similar way. In dogs, clarithromycin caused contractions and discomfort, as did erythromycin [ ]. In healthy volunteers, oral clarithromycin 250 mg bd caused a statistically significant increase in the number of postprandial antral contractions and antral motility [ ]. Clarithromycin can cause abdominal pain, but less often than erythromycin [ ].

In a randomized comparison of oral telithromycin 800 mg/day for 5 or 7 days and oral clarithromycin 500 mg bd for 10 days in 575 patients, 257 (45%) had at least one treatment-related adverse event [ ]. The most frequent adverse effects were gastrointestinal (diarrhea, nausea, and dysgeusia). None of the patients taking clarithromycin withdrew because of gastrointestinal events.

Based on observations made in dogs and rabbits, clarithromycin is significantly less potent than azithromycin and erythromycin as an agonist for stimulation of smooth muscle contraction [ ]. Therefore, a lower rate of gastrointestinal adverse events would be expected with clarithromycin.

Pseudomembranous colitis is relatively rarely seen with macrolides, but has been reported with clarithromycin [ , ].

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