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fluconazole

Sold as Diflucan. Class: Imidazole and triazole derivatives; Triazole and tetrazole derivatives. First FDA approval 01/29/1990: 36 years on the US market.

This grade answers one narrow question: how strong is the public evidence and safety record behind this drug, and how clean is its money trail and court record? It is not a verdict on whether the drug is right for you.

B

Score breakdown (79/100)

Safety ×35%
B
Evidence ×25%
D
Regulatory ×15%
B
Money & lawsuits ×15%
A
Options ×10%
A

Safety: 76

Evidence: 59

Regulatory history: 86

Money & lawsuits: 100

Options: 100

Independent reviews and post-approval warnings

FDA Drug Safety Communications

Warnings the FDA chose to announce publicly after approval, as opposed to quiet label edits. Class-wide items name the drug's class, not this drug specifically.

WHO Essential Medicine

Listed on the WHO Model List of Essential Medicines: a global expert panel judged it among the medicines a health system should always have, on evidence of value, not marketing.

What the FDA label says

Approved uses

INDICATIONS AND USAGE DIFLUCAN (fluconazole) is indicated for the treatment of: 1. Vaginal candidiasis (vaginal yeast infections due to Candida ). 2. Oropharyngeal and esophageal candidiasis. In open noncomparative studies of relatively small numbers of patients, DIFLUCAN was also effective for the treatment of Candida urinary tract infections, peritonitis, and systemic Candida infections including candidemia, disseminated candidiasis, and pneumonia. 3. Cryptococcal meningitis. Before prescribing DIFLUCAN (fluconazole) for AIDS patients with cryptococcal meningitis, please see CLINICAL STUDIES section. Studies comparing DIFLUCAN to amphotericin B in non-HIV infected patients have not been conducted. Prophylaxis: DIFLUCAN is also indicated to decrease the incidence of candidiasis in patients undergoing bone marrow transplantation who receive cytotoxic chemotherapy and/or radiation therapy. Specimens for fungal culture and other relevant laboratory studies (serology, histopathology) should be obtained prior to therapy to isolate and identify causative organisms. Therapy may be instituted before the results of the cultures and other laboratory studies are known; however, once these re...

Contraindications

CONTRAINDICATIONS DIFLUCAN (fluconazole) is contraindicated in patients who have shown hypersensitivity to fluconazole or to any of its excipients. There is no information regarding cross-hypersensitivity between fluconazole and other azole antifungal agents. Caution should be used in prescribing DIFLUCAN to patients with hypersensitivity to other azoles. Coadministration of other drugs known to prolong the QT interval and which are metabolized via the enzyme CYP3A4 such as erythromycin, pimozide, and quinidine are contraindicated in patients receiving fluconazole. (See CLINICAL PHARMACOLOGY: Drug Interaction Studies and PRECAUTIONS .)

Warnings and precautions

WARNINGS (1) Hepatic injury: DIFLUCAN should be administered with caution to patients with liver dysfunction. DIFLUCAN has been associated with rare cases of serious hepatic toxicity, including fatalities primarily in patients with serious underlying medical conditions. In cases of DIFLUCAN-associated hepatotoxicity, no obvious relationship to total daily dose, duration of therapy, sex, or age of the patient has been observed. DIFLUCAN hepatotoxicity has usually, but not always, been reversible on discontinuation of therapy. Patients who develop abnormal liver function tests during DIFLUCAN therapy should be monitored for the development of more severe hepatic injury. DIFLUCAN should be discontinued if clinical signs and symptoms consistent with liver disease develop that may be attributable to DIFLUCAN. (2) Anaphylaxis: In rare cases, anaphylaxis has been reported. (3) Dermatologic: Exfoliative skin disorders during treatment with DIFLUCAN have been reported. Fatal outcomes have been reported in patients with serious underlying diseases. Patients with deep seated fungal infections who develop rashes during treatment with DIFLUCAN should be monitored closely and the drug discontinu...

Adverse reactions (label)

ADVERSE REACTIONS DIFLUCAN is generally well tolerated. In some patients, particularly those with serious underlying diseases such as AIDS and cancer, changes in renal and hematological function test results and hepatic abnormalities have been observed during treatment with fluconazole and comparative agents, but the clinical significance and relationship to treatment is uncertain. In Patients Receiving a Single Dose for Vaginal Candidiasis: During comparative clinical studies conducted in the United States, 448 patients with vaginal candidiasis were treated with DIFLUCAN, 150 mg single dose. The overall incidence of side effects possibly related to DIFLUCAN was 26%. In 422 patients receiving active comparative agents, the incidence was 16%. The most common treatment-related adverse events reported in the patients who received 150 mg single dose fluconazole for vaginitis were headache (13%), nausea (7%), and abdominal pain (6%). Other side effects reported with an incidence equal to or greater than 1% included diarrhea (3%), dyspepsia (1%), dizziness (1%), and taste perversion (1%). Most of the reported side effects were mild to moderate in severity. Rarely, angioedema and anaphyla...

Source: FDA SPL label for Diflucan (Roerig), effective 20260402. Full label on DailyMed.

Side-effect reports sent to the FDA

These are counts of reports people filed, not rates of harm. Anyone can file one, and nobody checks whether the drug was the cause. Millions of doses are taken for every report sent, so the useful part is how this drug compares with the average across all drugs.

55,947reports that mention this drug
55,346of those blame this drug, not another one the person was taking
83%of reports describe a serious outcome, such as a hospital stay (average for all drugs: 57%)
16.1%of reports include a death, from any cause (average for all drugs: 9.1%)

Problems reported most often

Drug Ineffective · 4,724Off Label Use · 4,543Pyrexia · 3,076Nausea · 2,887Fatigue · 2,730Diarrhoea · 2,708Drug Interaction · 2,466Headache · 2,465Pain · 2,367Acute Kidney Injury · 2,299Pneumonia · 2,155Rash · 2,046Febrile Neutropenia · 2,013Dyspnoea · 1,783Death · 1,758

Reports per year

20192020202120222023202420252026
6,0375,6095,1954,5204,1534,4554,3021,807

2,727 reports blaming this drug for every million Medicare prescriptions filled, which is 1.0× the typical drug on this site. (10,262 reports in 2024–2026, against 3,763,535 Medicare fills in one year. This is the one number here that accounts for how many people take the drug.)

Source: the FDA's Adverse Event Reporting System (FAERS). Reports are voluntary and unverified. Drugs that are prescribed a lot, in the news, or in lawsuits attract more reports, so the percentages are compared with the whole database to correct for that partly, not fully.

Recalls and regulatory record

10recall actions on file
3 / 38brand / generic applications
15label changes since 2021
NoREMS program
DateClassFirmReason
05/2017Class IIBaxter Healthcare CorporationLack of assurance of sterility: customer complaints received for the presence of leaks.
01/2017Class IIThe Harvard Drug GroupFailed Dissolution Specifications
01/2017Class IIThe Harvard Drug GroupFailed Dissolution Specifications
12/2016Class IIDr. Reddy's Laboratories, Inc.Failed Dissolution Specifications; 18 month stability time point
12/2016Class IIDr. Reddy's Laboratories, Inc.Failed Dissolution Specifications; 18 month stability time point
12/2016Class IIDr. Reddy's Laboratories, Inc.Failed Dissolution Specifications; 18 month stability time point
12/2016Class IIDr. Reddy's Laboratories, Inc.Failed Dissolution Specifications; 18 month stability time point
12/2016Class IIBaxter Healthcare CorporationLack of Assurance of Sterility: confirmed customer complaints of leaking bags.
12/2014Class IIBaxter Healthcare Corp.Lack of Assurance of Sterility: Complaints of leaks due to an incomplete seal at the bag seam.
01/2014Class IIPfizer Inc.Defective Container: Tamper evident ring failures discovered on some bottles.

Class I = reasonable probability of serious harm. Class II = temporary or reversible harm. Class III = unlikely to harm. Most generic recalls are manufacturing or labeling defects for one lot, not a verdict on the molecule.

Evidence base

374randomized trials (PubMed)
41systematic reviews
308registered trials
25%of completed trials posted results
8%terminated or withdrawn
50%industry-funded

Independent Cochrane reviews

Counts measure how much evidence exists and how transparent it is, not how big the benefit is. For that, ask your prescriber: if 100 people like me took this, how many would get better because of it, and how many would be harmed? (Doctors call these the "number needed to treat" and "number needed to harm.") It differs by condition and is the number drug ads leave out. Sources: PubMed, ClinicalTrials.gov.

Money and lawsuits

In 2024, drug companies reported $0 in payments to US physicians and hospitals tied to this drug across 0 transactions.

No pending federal MDL names this drug or its brands.

Not named in any federal pharmaceutical settlement of $100M or more on record.

Sources: CMS Open Payments (Sunshine Act); Judicial Panel on Multidistrict Litigation pending docket list; DOJ settlements as tabulated on Wikipedia with links to the primary record. State-court and individual suits are not included.

Who takes it and what it costs

2,157,994Medicare Part D patients (2024)
3,763,535prescriptions filled
$10average cost per fill
$38Mtotal Medicare spend
ProductFills$/fill
Fluconazole3,763,187$10
Diflucan348$963

Same-class alternatives

bifonazoleeconazoleefinaconazolefenticonazoleflutrimazoleisavuconazoleisoconazoleitraconazoleluliconazolemiconazoleomoconazoleoteseconazoleoxiconazoleposaconazolesertaconazolesulconazolethiabendazoletioconazolevoriconazole

Same ATC pharmacological class, graded ones first, best grade at the top. Being in the same class does not make them interchangeable for your condition; it makes them worth asking about.

Questions to ask your prescriber

  1. In 2016 the FDA issued a safety communication about this drug (FDA to review study examining use of oral fluconazole (Diflucan) in pregnancy). Does that risk apply to me?
  2. The most-reported problems in FDA's adverse event data are pyrexia, nausea. How would we recognize and handle those?
  3. Off-label use is among the most-reported items for this drug. Is my use on-label, and if not, what evidence supports it?
  4. Why this one over bifonazole, clotrimazole, econazole? What would make you pick one of those instead?
  5. What result are we expecting, by when, and what is the plan if it does not happen?
  6. If 100 people like me took this drug, how many would actually get better because of it, and how many would be harmed by it? (Doctors call these the number needed to treat and the number needed to harm.)