Generic name
Maraviroc: adverse event reports filed with FDA
1,360 reports list it as a suspect or interacting product, 2007–2026. Also reported as Tab Maraviroc, Maraviroc Tablet.
- 1,360
- reports as suspect product
- 0% of all reports · about 73 a year
- 30
- reports, 12 months to June 2026
- 31 in the 12 months before
- 96.9%
- marked serious by the reporter
- 57.4% across all reports
- 14.9%
- record death among outcomes, as reported
- 202 reports · not verified by FDA
Between October 2007 and June 2026, 1,360 adverse event reports received by FDA list maraviroc, a generic name as a suspect or interacting product. Reports that mention it only as a concomitant medication (402) are left out of every figure here.
In the 12 months to June 2026, 30 reports listed it, close to the 31 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 73 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The MedDRA terms listed most often are virologic failure (7.2%), viral mutation identified (6.4%) and pathogen resistance (6.1%). A report can list several reactions, so shares add to more than 100%; 361 different terms appear across these reports. Virologic failure is recorded in 7.2% of these reports, against 0% of all reports in the database.
96.9% of the reports are marked serious by the reporter; 14.9% record death among the outcomes and 44.3% record hospitalisation, as reported. 46.7% of the reports came from physicians, and the largest patient age group is 45 to 64 (28.8%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
2026 covers reports received through June 2026 only.
Reactions recorded in the reports
share of Maraviroc reports recording the termall reports in the database
- Virologic failure7.2%98
- Viral mutation identified6.4%87
- Pathogen resistance6.1%83
- Drug resistance4.8%65
- Drug ineffectivethe medicine did not work as expected4%55
- Treatment noncompliancethe treatment was not taken as directed3.8%52
- Exposure during pregnancythe medicine was taken during pregnancy3.2%43
- Myocardial infarctionheart attack2.8%38
- Condition aggravatedthe condition being treated got worse2.6%35
- Pyrexiafever2.6%35
- Off label useused for a purpose or in a way not on the label2.5%34
- Deaththe patient died; cause not stated by this term2.4%33
- Drug interactionan interaction between medicines2.3%31
- Nauseafeeling sick2.3%31
- Maternal exposure during pregnancythe mother took the medicine during pregnancy2.1%28
- Abortion spontaneousmiscarriage1.8%25
- Treatment failurethe treatment did not work1.8%25
- Pneumonialung infection1.7%23
- Acute kidney injurysudden loss of kidney function1.5%21
- Foetal exposure during pregnancythe unborn baby was exposed to the medicine1.5%20
- Pancytopenialow counts of all blood cells1.5%20
- Urinary tract infectionbladder or urinary infection1.5%20
- Weight decreasedweight loss1.5%20
- Blood HIV RNA increased1.4%19
- Dizzinesslight-headedness or unsteadiness1.4%19
- Falla fall1.4%19
- Malaisegeneral feeling of being unwell1.4%19
- Depressionlow mood1.3%18
- Kaposi's sarcoma1.3%18
- Toxicity to various agentspoisoning or toxic effect of one or more substances1.3%18
Top 30 of 361 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 27.9% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Hiv infection | 934 | 68.7% |
| Hiv test positive | 35 | 2.6% |
| Prophylaxis against HIV infection | 17 | 1.3% |
| Prophylaxis against graft versus host disease | 12 | 0.9% |
| Antiretroviral therapy | 11 | 0.8% |
| Perinatal HIV infection | 9 | 0.7% |
The indication field is filled in by the reporter and is often blank; shares are of all 1,360 reports.
In context
| Measure | Maraviroc | All reports |
|---|---|---|
| Reports as suspect product | 1,360 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 30 | 1,332,454 |
| Marked serious | 96.9% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 149 | 91 |
| Hospitalisation recorded, per 1,000 reports | 443 | 213 |
| Consumer-filed share | 10.1% | 45.8% |
| Top term, share of reports | Virologic failure 7.2% | 0% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Maraviroc reports
How many adverse event reports has FDA received for Maraviroc?
1,360 reports list Maraviroc as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 30 of them arrived in the latest 12 months. Another 402 list it only as a concomitant medication.
What reactions are recorded in Maraviroc reports?
virologic failure (7.2%), viral mutation identified (6.4%), pathogen resistance (6.1%), drug resistance (4.8%) and drug ineffective (4%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Maraviroc was responsible.
How serious are the reports?
96.9% are marked serious by the reporter. Among the outcomes recorded, 14.9% of reports include death and 44.3% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
physician (46.7%), other health professional (35.8%) and consumer or non-health professional (10.1%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Maraviroc rising?
30 reports in the 12 months to June 2026, close to the 31 of the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Maraviroc was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Maraviroc?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Maraviroc as a suspect or interacting product; reports listing it only as a concomitant medication (402) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.