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PharmaceuticalReviewed July 2026 · v1.0

Antibiotics

Life-saving for bacterial infection, useless against viruses — and the hard part is telling which is which

That antibiotics cure bacterial infections is as well established as anything in medicine, and for serious infection they are life-saving. It is equally well established that they do not help viral infections, and that most of the conditions people request them for — the common cold, most acute bronchitis, most acute sinusitis, most sore throats — are viral or self-limiting, so antibiotics offer little or no benefit and measurable harm. Their harms are real and often underestimated: a roughly two-fold increase in the reader's own risk of carrying resistant bacteria for months afterward, Clostridioides difficile infection, allergic reactions, and specific class dangers such as tendon rupture and aortic injury with fluoroquinolones. Delayed ('back-up') prescribing safely cuts antibiotic use without worsening outcomes, and the old blanket instruction to 'always finish the course to prevent resistance' is not well supported — though 'take them exactly as prescribed' still is.

How confident is BioSignal?

Our overall position, and how sure we are of it across each dimension — including where we are not sure at all.

High confidence

That antibiotics cure bacterial infections is as well established as anything in medicine, and for serious infection they are life-saving. It is equally well established that they do not help viral infections, and that most of the conditions people request them for — the common cold, most acute bronchitis, most acute sinusitis, most sore throats — are viral or self-limiting, so antibiotics offer little or no benefit and measurable harm. Their harms are real and often underestimated: a roughly two-fold increase in the reader's own risk of carrying resistant bacteria for months afterward, Clostridioides difficile infection, allergic reactions, and specific class dangers such as tendon rupture and aortic injury with fluoroquinolones. Delayed ('back-up') prescribing safely cuts antibiotic use without worsening outcomes, and the old blanket instruction to 'always finish the course to prevent resistance' is not well supported — though 'take them exactly as prescribed' still is.

Well-supported by consistent, high-quality evidence.

Human Evidence

High confidence

Enormous. Decades of randomised trials and Cochrane reviews across every common infection, plus population-scale data on resistance and harm. Few interventions are this thoroughly studied.

Clinical Benefit

High confidence

For bacterial infection, decisive and often life-saving. For the viral and self-limiting illnesses people most often take them for, the benefit is small to none — the confidence here is high precisely because the trials are clear that antibiotics do little for a cold or acute bronchitis.

Safety Profile

Caution

Consequential and frequently underestimated: individual resistance for months after a course, C. difficile, allergy (from rash to anaphylaxis), gut-microbiome disruption, and drug-specific harms — fluoroquinolone tendon and aortic injury, macrolide QT effects. A caution rating because the harms are clear, not because they are uncertain.

Biological Role

High confidence

Well understood. Antibiotics kill or inhibit bacteria through defined mechanisms (cell-wall synthesis, protein synthesis, DNA replication). They have no mechanism of action against viruses — which is why they cannot help a cold, however severe it feels.

Research Activity

High

Intense: antimicrobial resistance, stewardship, shorter-course trials, penicillin-allergy de-labelling, and rapid point-of-care tests to tell bacterial from viral. The field is mature and moving.

Consensus

High confidence

Guidelines worldwide agree: reserve antibiotics for likely bacterial infection, prefer no-antibiotic or delayed strategies for self-limiting respiratory illness, use the narrowest effective agent, and treat antimicrobial resistance as a first-order public-health threat.

Where the evidence stands today

How mature the science is, what kinds of evidence exist, and — the part nobody else prints — what is still missing.

9/9

steps proven in humans

Evidence-rich

Proven at every applicable step — rare, and worth noticing.

  1. Guideline / regulatory support

    Proven

    Recommended, with strong stewardship conditions: right indication, narrowest agent, shortest effective course.

  2. Clinical outcomes

    Proven

    Cure of bacterial infection and prevention of its complications; on the harm side, resistance, C. difficile and drug-specific injury.

  3. Large human RCTs

    Proven

    Including the trials underpinning delayed-prescribing and short-course strategies.

  4. Small human outcome trials

    Proven

    Numerous across every common infection.

  5. Human safety data

    Proven

    Extensive — allergy, C. difficile, individual resistance, and class-specific harms are all quantified.

  6. Human biomarker / pharmacology

    Proven

    Pharmacokinetics, susceptibility testing and resistance mechanisms are well described and clinically used.

  7. Animal

    Proven

    Substantial.

  8. Cell / in vitro

    Proven

    Extensively characterised, including the biochemistry of resistance.

  9. Mechanistic plausibility

    Proven

    Defined mechanisms against bacteria (cell wall, protein and DNA synthesis). No mechanism against viruses.

The bottom line

What we know, what we think, what we don't know — and what would change our mind.

What we know

Antibiotics cure bacterial infections and save lives — untreated bacterial pneumonia, sepsis, pyelonephritis and meningitis kill people. And they do nothing to a virus: a cold, the flu, and most coughs and sore throats will not respond, because there is no bacterium for the drug to act on.

What we think

Most respiratory infections people seek antibiotics for are viral or self-limiting, so a no-antibiotic or 'back-up' prescription is usually the right call — it cuts antibiotic use dramatically without increasing complications. The best available evidence also suggests the reflex 'always finish the whole course' rationale is weaker than we were taught, though following the specific instructions you were given still matters.

What we don't know

Whether a particular illness in a particular person is bacterial — that is exactly what an evidence library cannot tell you, and what an examination and sometimes a test can. Reliable, cheap, fast point-of-care tests to separate bacterial from viral at the bedside do not yet exist for most infections, which is why so much prescribing is a judgement call.

Active research

Antimicrobial stewardship, shorter treatment courses, penicillin-allergy de-labelling, rapid diagnostics, and new agents against resistant organisms. Resistance is outpacing the drug pipeline, which is the central problem the field is organised around.

What would change our mind

A cheap, fast, accurate test that tells bacterial from viral infection in the room would reshape prescribing overnight — turning most of these judgement calls into measurements. That, more than any new antibiotic, is what the honest version of this page is waiting for.

The biggest myth

Antibiotics will help my cold, cough or flu get better faster.

Not establishedHigh confidence

They will not, because these illnesses are viral and antibiotics have no action against viruses. A Cochrane review found no benefit of antibiotics for the common cold — symptoms were no more likely to clear (risk ratio 0.83, confidence interval crossing no effect) — while adults taking them had more than double the rate of adverse effects (RR 2.62). For acute bronchitis, another Cochrane review found no difference in overall clinical improvement (RR 1.07) and only a fraction of a day less coughing, bought at the price of a measurable excess of side effects (about one extra harmed for every 24 treated). The colour of your phlegm or mucus, incidentally, does not indicate a bacterial infection — green is not a prescription. If a cough or cold is not improving as expected, that is a reason to be assessed, not automatically a reason for antibiotics.

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Ask about Antibiotics

Why people take antibiotics

Popularity is not evidence — but it is not stupid either. This explains the interest on its own terms.

Because almost everyone takes them, almost everyone has been told conflicting things about them, and the stakes feel high when you or your child is unwell. People arrive with a very specific set of questions — do I need them for this, will they make me better faster, do I have to finish the pack, am I really allergic, and are they doing me harm — and the information landscape around those questions is unusually poor, caught between 'antibiotics are miracle drugs, demand them' and 'antibiotics are ruining the world, avoid them'. Both framings miss the real one, which is narrower and more useful: antibiotics are extraordinary drugs for the specific job of killing bacteria, and most of the time people want them, that is not the job at hand.

If you're here because…

Jump straight to the part of the evidence that answers your question.

Approval, safety and regulatory

What it is approved for, who should be careful, what remains unknown — and the limits of what this evidence can tell you.

Regulatory status

FDA-approved drug class; prescription-only in most countries

Availability

Prescription-only in most countries (over the counter in some)

Sport (WADA)

Not prohibited

Known safety profile

Well characterised and frequently underestimated. Resistance: an individual course roughly doubles the odds of carrying resistant bacteria for the following months. Clostridioides difficile: antibiotics are the leading modifiable cause, highest with clindamycin, cephalosporins (especially third-generation) and fluoroquinolones. Allergy: reactions range from rash to anaphylaxis; antibiotics are among the commonest causes of serious drug hypersensitivity. Class-specific harms: fluoroquinolones carry boxed warnings for tendinitis and tendon rupture, aortic aneurysm and dissection, peripheral neuropathy and serious neuropsychiatric effects; macrolides (e.g. azithromycin) are associated with a small increase in cardiovascular death via QT prolongation. Microbiome: broad courses disrupt the gut flora, which mostly but not always fully recovers.

Common issues

  • Diarrhoea, nausea and other gastrointestinal upset
  • Thrush and other Candida overgrowth
  • Allergic reactions, from rash to (rarely) anaphylaxis
  • Clostridioides difficile infection, particularly with broad-spectrum agents
  • Carriage of resistant bacteria for months after a course

Use caution if

  • People with a genuine, severe antibiotic allergy (anaphylaxis, blistering skin reactions)
  • Older adults and those with tendon, aortic or aneurysm risk (fluoroquinolones)
  • People with prolonged QT or on other QT-prolonging drugs (macrolides)
  • People at high risk of C. difficile (older, hospitalised, prior episode)
  • Anyone for whom the illness is likely viral — where the risk-benefit is simply unfavourable

Long-term unknowns

The cumulative long-term consequences of repeated microbiome disruption from ordinary courses across a lifetime are not well characterised. In one study nine common gut species remained undetectable six months after a single short broad-spectrum course.

Limits of this evidence

Most efficacy trials enrol people already suspected of bacterial infection, so they speak to 'does the antibiotic help this infection', not 'is this person's illness bacterial' — the harder question in practice. Resistance data are largely observational at the individual level. And the absence of a cheap, accurate bedside bacterial-versus-viral test means much real-world prescribing is a probabilistic judgement rather than a measured one.

Full regulatory and sport detail
Regulatory approval
FDA-approved and in worldwide clinical use. Prescription-only in most countries, though some antibiotics are sold without prescription in parts of the world — a practice that itself contributes to resistance.
Approved indication
Treatment (and in defined cases prevention) of bacterial infection.
Research chemical
N/A — approved medicines.
Sport (WADA)
Not prohibited in or out of competition.
Publication note
Stewardship guidance, resistance patterns and specific safety warnings (for example the fluoroquinolone boxed warnings) evolve. Re-confirm current FDA, EMA, NICE, CDC and WHO positions at each review.

Demand, separated from evidence

Every claim people make about this, counted against what the evidence actually showed.

BioSignal evaluated 7 popular claims about antibiotics.

Here is where each one landed — including the claims of harm, where “not established” is reassuring rather than damning.

Mixed evidence
3
Not established
4

Popularity is not evidence. This is simply a count of every claim BioSignal evaluated on this page, sorted by what the evidence actually showed — the full reasoning behind each verdict is in the Evidence Review below.

Mixed evidence

  • I was told I'm allergic to penicillin, so I can never have it.
  • Antibiotics work for sinus infections.
  • A sore throat needs antibiotics.

Not established

  • Antibiotics will help my cold, cough or flu get better faster.
  • You must always finish the entire course, or you'll cause antibiotic resistance.
  • Antibiotics are basically harmless — it can't hurt to take them just in case.
  • Antibiotic resistance is a hospital problem — my own prescriptions don't really affect it.

The evidence review

Every claim with the reasoning behind its verdict, the doses actually studied, where scientists agree and disagree, and the questions still open.

What people claim

Every popular claim, with BioSignal’s verdict and how confident we are in it. The verdicts are always visible; open any claim to read the evidence behind it.

You must always finish the entire course, or you'll cause antibiotic resistance.Not establishedModerate confidence

This specific rationale is not well supported, and it may be backwards. A prominent BMJ analysis argued that the 'complete the course' message rests on little evidence, and that for many infections longer exposure drives more resistance, not less — shorter courses are increasingly shown to work just as well. Two cautions keep this honest. First, this is an argument about the RESISTANCE justification, not a licence to stop the moment you feel better and self-manage: the current, correct advice is to take antibiotics exactly as prescribed, because the right duration is the one your clinician chose for your infection, and for some infections (tuberculosis is the clearest) completion genuinely does matter. Second, changing course length is a decision for the prescriber, not the patient. So: follow the instructions you were given — but the folk belief that a fixed 'full course' is a law of nature protecting the world from resistance is not one.

Antibiotics are basically harmless — it can't hurt to take them just in case.Not establishedHigh confidence

It can, in several concrete ways. An antibiotic course roughly doubles your own chance of carrying resistant bacteria for the following months (in urinary bacteria, odds about 2.5-fold within two months, still raised at a year). Antibiotics are the leading modifiable cause of Clostridioides difficile, a serious gut infection — the risk is highest with clindamycin, cephalosporins and fluoroquinolones. They disrupt the gut microbiome, which mostly but not fully recovers: in one study, nine common gut species were still undetectable six months after a short course. Allergic reactions range from rash to anaphylaxis, and specific classes carry specific dangers — fluoroquinolones alone carry FDA boxed warnings for tendon rupture, aortic aneurysm and dissection, nerve damage and serious mental-health effects. 'Just in case' is not a free action.

I was told I'm allergic to penicillin, so I can never have it.MixedHigh confidence

Very possibly you can. About one in ten people carries a penicillin-allergy label, but when those people are formally assessed, the large majority — well over 90% — are not truly allergic; genuine penicillin hypersensitivity affects under 5%. Many labels come from a childhood rash that was the infection, not the drug, and true allergy also fades: around 80% of genuinely allergic people tolerate penicillin again after a decade. This matters because the label is not harmless — it pushes people onto broader, less effective, and sometimes more dangerous alternatives, and is associated with more MRSA and C. difficile. An incorrect penicillin-allergy label is worth having formally re-evaluated rather than carried for life. (A label that followed a severe reaction — swelling, breathing difficulty, blistering — is different and must be taken seriously; this is a conversation for a clinician, not a decision to make alone.)

Antibiotics work for sinus infections.MixedHigh confidence

Rarely enough to be worth it. Most acute sinusitis is viral or self-limiting: in trials, about 46% of people are better within a week and 64% within two weeks with no antibiotic at all. Antibiotics add only a small absolute benefit — roughly one extra person cured for every 17 treated — while causing side effects in about one in eight, so across a typical group the harm outweighs the benefit. Guidelines reserve antibiotics for the minority with features suggesting bacterial infection (severe, prolonged, or 'double-sickening' illness that improves then clearly worsens). For most people with a blocked, painful few days, the honest answer is that antibiotics are not the treatment, and symptom relief plus time is.

Antibiotic resistance is a hospital problem — my own prescriptions don't really affect it.Not establishedHigh confidence

Your own prescriptions affect your own body, directly and measurably. A systematic review found that an individual who takes an antibiotic in primary care is left with a substantially higher chance of carrying resistant bacteria — the effect is strongest in the first month and still detectable up to a year later. Scaled across a population, that is the engine of resistance: an estimated 1.27 million deaths worldwide in 2019 were directly attributable to bacterial antimicrobial resistance, and nearly five million were associated with it. Roughly 30% of outpatient antibiotic prescriptions are estimated to be unnecessary. Resistance is not only a hospital's problem or a future one — it is a cumulative consequence of ordinary prescribing, which is exactly why using antibiotics only when they will help is framed as a shared responsibility rather than an individual inconvenience.

A sore throat needs antibiotics.MixedHigh confidence

Usually not. Most sore throats are viral, and even when antibiotics are given they shorten symptoms by only about 16 hours on average. Their real value is narrower: reducing the uncommon complications of streptococcal (strep) throat — acute rheumatic fever and abscess — which is why clinicians use scoring tools to estimate the chance of a bacterial cause before prescribing, rather than treating every sore throat. In settings where rheumatic fever is rare, most sore throats are managed with pain relief and time. The question is not whether the throat hurts; it is whether the cause is the bacterium antibiotics act on.

Doses used in human studies

What was actually given to participants in the research. These are descriptions of studies, not recommendations.

Adults and children with the common cold or acute purulent rhinitis

Intervention
Antibiotics vs placebo (Cochrane review)
Dose
Various regimens
Duration
Typical course lengths
Outcome
No benefit for symptom persistence (RR 0.83); adults had more adverse effects (RR 2.62)
Notes
The evidence base for the single most common reason people request antibiotics — and it shows harm without benefit.

Adults and children with acute bronchitis

Intervention
Antibiotics vs placebo (Cochrane review)
Dose
Various regimens
Duration
Typical course lengths
Outcome
No difference in global improvement (RR 1.07); cough NNTB 6; adverse-effect NNTH 24
Notes
A fraction of a day less coughing, offset by a clear excess of side effects. Not a bacterial illness in most cases.

Adults with clinically or radiologically diagnosed acute sinusitis

Intervention
Antibiotics vs placebo (Cochrane review)
Dose
Various regimens
Duration
Typical course lengths
Outcome
46% cured at 1 week / 64% at 2 weeks without antibiotics; NNT 17; NNH 8
Notes
Harms roughly twice as common as benefit across a typical treated group.

Patients with respiratory infections in primary care

Intervention
Immediate vs delayed ('back-up') vs no antibiotics (Cochrane review)
Dose
Prescription strategy, not a dose
Duration
Single illness episode
Outcome
Antibiotic use: immediate ~93% · delayed ~29% · none ~13%; no difference in complications
Notes
The evidence behind back-up prescribing: it cuts antibiotic use to a third with no measured cost in complications or meaningful loss of satisfaction.

Where scientists agree — and don’t

Agreed

  • Antibiotics are life-saving for bacterial infection and have no effect on viral illness
  • The common cold, most acute bronchitis, most acute sinusitis and most sore throats do not need antibiotics
  • No-antibiotic or delayed ('back-up') prescribing is appropriate for self-limiting respiratory infection
  • Antimicrobial resistance is a first-order global public-health threat
  • Use the narrowest effective agent for the shortest appropriate duration
  • Incorrect penicillin-allergy labels should be re-evaluated rather than carried for life

Debated

  • The optimal duration of treatment for many infections — the direction is toward shorter
  • How aggressively to pursue penicillin-allergy de-labelling, and in which settings
  • Which rapid diagnostics are accurate and cheap enough to change bedside prescribing

Unknown

  • Whether a given infection is bacterial without examination and, often, testing
  • The long-term consequences of repeated microbiome disruption from ordinary courses

What remains unknown

  • Can a cheap, fast, accurate point-of-care test reliably separate bacterial from viral infection at the bedside?
  • What is the shortest effective course for each common infection?
  • How much of the resistance burden could be averted by eliminating clearly unnecessary prescriptions?
  • Does routine penicillin-allergy de-labelling improve outcomes at population scale?

Questions people actually ask

Will antibiotics help my cold or cough?

Almost certainly not. Colds and most coughs are caused by viruses, and antibiotics have no effect on viruses — a Cochrane review found no benefit for the common cold and, in adults, more than double the rate of side effects. The urge to 'do something' is understandable, but for a viral illness the antibiotic is not doing the something you want; it is only adding risk. If a cough lasts beyond about three weeks, comes with breathlessness, chest pain, or coughing up blood, or you feel very unwell, that is a reason to be seen — not automatically a reason for antibiotics, but a reason for assessment.

Do I have to finish the whole course of antibiotics?

Take them exactly as your prescriber told you — but the familiar reason given for it is shakier than you have been told. The idea that stopping early breeds resistance is not well supported, and for many infections shorter courses work just as well; a widely discussed BMJ analysis argued the 'always complete the course' message should be retired. That is not permission to stop the moment you feel better and manage it yourself: the right length is the one chosen for your specific infection, and for some (like tuberculosis) completion genuinely matters. The honest summary is: follow the instructions you were given, don't improvise, and don't treat a fixed 'full course' as a magic number.

I think I'm allergic to penicillin — is that a problem?

It might be less of one than you think. About 10% of people carry a penicillin-allergy label, but when tested, more than 90% turn out not to be truly allergic — many labels trace back to a childhood rash that was actually the infection. This is worth sorting out, because the label is not free: it pushes you onto broader, sometimes less effective and riskier antibiotics, and is linked to more resistant infections. If your 'allergy' was a mild or vague reaction long ago, ask about having it formally assessed. If it was a severe reaction — facial swelling, difficulty breathing, or blistering skin — take it seriously and make sure it stays on your record; that is not the label to challenge on your own.

Are antibiotics dangerous?

They are not harmless, which is the point people miss. Beyond allergic reactions, a course roughly doubles your own chance of carrying resistant bacteria for months, is the leading cause of Clostridioides difficile (a serious gut infection), and disturbs the gut microbiome in ways that do not always fully reverse. Some classes carry specific dangers: fluoroquinolones (such as ciprofloxacin) have official warnings for tendon rupture, aortic injury, nerve damage and mental-health effects, and are reserved for when nothing safer will do. None of this means antibiotics are bad — for a bacterial infection the benefit vastly outweighs these risks. It means taking them 'just in case' for an illness that will not respond is a poor trade.

How do I know if my infection is bacterial or viral?

Often you cannot tell from home, and neither can a search engine — which is exactly why this is a question for a clinician rather than a page. Some clues make a virus more likely (a gradual cold-like illness with runny nose and cough), and some features raise concern for a bacterial cause or a complication (high or prolonged fever, feeling very unwell, symptoms that improve then sharply worsen, or breathlessness). But these overlap, and reliable bedside tests to separate the two do not yet exist for most infections. If you are unsure or getting worse, be assessed. BioSignal can tell you what the evidence says about antibiotics; it cannot tell you what you have.

Practical takeaways

  • Antibiotics are life-saving for bacterial infection and do nothing for a virus — the hard part is telling which you have, and that needs a clinician.
  • Most colds, coughs, sore throats and sinus infections are viral or self-limiting; antibiotics add little and carry real harm.
  • A course roughly doubles your own risk of carrying resistant bacteria for months — resistance is personal, not only a hospital problem.
  • Take antibiotics exactly as prescribed — but the blanket 'always finish the course to stop resistance' rule is not well evidenced.
  • Most 'penicillin allergy' labels are not real; an incorrect one is worth re-checking, because it pushes you toward worse drugs.

How it works

The mechanism comes last on purpose. A compelling explanation of how something might work is the easiest part of the story to tell, and the part most likely to outlive the evidence for it.

Well understood. Antibiotics kill or inhibit bacteria through defined mechanisms (cell-wall synthesis, protein synthesis, DNA replication). They have no mechanism of action against viruses — which is why they cannot help a cold, however severe it feels.

How we found out

  1. 1928–1945 — penicillin

    Fleming's observation and the wartime scale-up turn bacterial infection from a common killer into a treatable illness — arguably the single greatest advance in the history of medicine.

  2. 2010 — resistance is personal

    A BMJ systematic review shows that an individual's own primary-care antibiotic course measurably raises their risk of carrying resistant bacteria for months — resistance is not only a hospital phenomenon.

  3. 2016 — the scale of overuse

    A JAMA study estimates that about 30% of US outpatient antibiotic prescriptions are unnecessary — a large, addressable driver of resistance.

  4. 2017 — 'the course has had its day'

    A BMJ analysis challenges the entrenched 'always finish the course to prevent resistance' message, arguing shorter courses often suffice and longer exposure can drive resistance.

  5. 2022 — the global toll

    The GRAM study estimates 1.27 million deaths in 2019 directly attributable to bacterial antimicrobial resistance, and 4.95 million associated with it — placing AMR among the leading global causes of death.

References

Verified sources. BioSignal does not print a citation it has not checked.

  1. 01

    Antibiotics for the common cold and acute purulent rhinitis

    Cochrane Database Syst Rev 6:CD000247 · 2013

  2. 02

    Antibiotics for acute bronchitis

    Cochrane Database Syst Rev 6:CD000245 · 2017

  3. 03

    Antibiotics for acute rhinosinusitis in adults

    Cochrane Database Syst Rev 9:CD006089 · 2018

  4. 04

    Antibiotics for sore throat

    Cochrane Database Syst Rev 11:CD000023 · 2013

  5. 05

    Immediate versus delayed versus no antibiotics for respiratory infections

    Cochrane Database Syst Rev 10:CD004417 · 2023

  6. 06

    Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis

    BMJ 340:c2096 · 2010

  7. 07

    Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis (GRAM)

    Lancet 399(10325):629-655 · 2022

  8. 08

    Prevalence of inappropriate antibiotic prescriptions among US ambulatory care visits, 2010-2011

    JAMA 315(17):1864-1873 · 2016

  9. 09

    Antibiotics and hospital-acquired Clostridium difficile infection: update of systematic review and meta-analysis

    J Antimicrob Chemother 69(4):881-891 · 2014

  10. 10

    Evaluation and management of penicillin allergy: a review

    JAMA 321(2):188-199 · 2019

  11. 11

    Antibiotic allergy

    Lancet 393(10167):183-198 · 2019

  12. 12

    The antibiotic course has had its day

    BMJ 358:j3418 · 2017

  13. 13

    Azithromycin and the risk of cardiovascular death

    N Engl J Med 366(20):1881-1890 · 2012

  14. 14

    Recovery of gut microbiota of healthy adults following antibiotic exposure

    Nat Microbiol 3(11):1255-1265 · 2018

  15. 15

    FDA-approved prescribing information, ciprofloxacin — boxed warning (tendinitis and tendon rupture, peripheral neuropathy, CNS effects, aortic aneurysm and dissection)

    FDA · 2024

  16. 16

    Antimicrobial resistance (fact sheet)

    WHO · 2023

  17. 17

    Respiratory tract infections (self-limiting): prescribing antibiotics (CG69)

    NICE guideline CG69 · 2008

Version history

  • 1.0

    Initial publication. Fixes the live 'antibiotics → Respiratory Infections' misroute. All references verified to source. Review cadence: Annually — resistance data and stewardship guidance move.