CD52-directed cytolytic antibody adverse event reports that FDA received for the drugs of this class
- Kind of class
- Pharmacologic class (FDA Established Pharmacologic Class)
- Drug pages
- 3
What a report is
A report is not proof that the drug was the cause of the event.
FDA says:
Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product.
Source: openFDA, Drug Adverse Event Overview, section "Responsible use of the data". The site read the page on . The data have the reports that FDA received through .
FDA also says:
There is no certainty that the reported event (adverse event or medication error) was actually due to the product. FDA does not require that a causal relationship between a product and event be proven, and reports do not always contain enough detail to properly evaluate an event. The information in these reports has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of these events.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.
Source: openFDA, Response of the drug event API (meta.disclaimer). The site read the page on .
Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.
Reports on file
CD52-directed cytolytic antibody is a pharmacologic class: an FDA Established Pharmacologic Class. The class has 3 drug pages on this site.
From January 2004 to June 2026, FDA received 17,330 adverse event reports that name a drug of the class. In these reports the drug is a suspect or interacting product. A report that names two drugs of the class counts one time for each.
FDA received 513 reports in the 12 months to June 2026 and 550 in the 12 months before. FDA releases FAERS data every quarter, so the newest months are not complete. They grow in later releases.
The number of people who use the product is not in the data. A count is not a rate.
Pharmacologic class
The Established Pharmacologic Class (EPC) of FDA is the class on the label of a drug. The site puts a drug in the class that its reports have most often.
Data version
openFDA FAERS release of 1 Oct 2026. Reports received through 30 Jun 2026.
Drugs of the class
The rows are in order of name. A brand name and its generic name are separate rows, because reporters name them separately.
FDA says:
Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
Importantly, the AEMS data by themselves are not an indicator of the safety profile of the drug or biologic.
Source: FDA, FDA Adverse Event Monitoring System (AEMS) Public Dashboard. Content current as of . The site read the page on .
| Drug | Name type | Reports | Reports, 12 months to June 2026 |
|---|---|---|---|
| Alemtuzumab | Generic name | 8,610 | 426 |
| CampathAlemtuzumab | Brand name | 2,751 | 38 |
| LemtradaAlemtuzumab | Brand name | 5,969 | 49 |
Reaction lookup
These are the reaction terms that the reports of the class record. Type a term or a plain word to find its count.
What this list leaves out
The table lists the 1,484 reaction terms that 5 or more reports record. A term with fewer than 5 reports is not in the table.
The site keeps reaction terms for 17,298 of the 17,330 reports (99.8%).
The reports of the other years are not in the counts.
So a count in the table can be lower than the count of FDA.
The table shows the first 50 of 1,484 terms.
| Reaction term (MedDRA) and plain meaning | Reports | Share of the 17,330 reports |
|---|---|---|
| Headachehead pain | 1,877 | 10.8% |
| Fatiguetiredness | 1,817 | 10.5% |
| Pyrexiafever | 1,705 | 9.8% |
| Off label useused for a purpose or in a way not on the label | 1,415 | 8.2% |
| Rashskin rash | 1,160 | 6.7% |
| Nauseafeeling sick | 1,142 | 6.6% |
| Dyspnoeashortness of breath | 963 | 5.6% |
| Astheniaweakness or lack of energy | 905 | 5.2% |
| Lymphocyte count decreased | 863 | 5% |
| Multiple sclerosis relapsea flare of multiple sclerosis | 857 | 4.9% |
| Drug ineffectivethe medicine did not work as expected | 796 | 4.6% |
| Urinary tract infectionbladder or urinary infection | 789 | 4.6% |
| Cytomegalovirus infection | 752 | 4.3% |
| Painpain, site not specified | 713 | 4.1% |
| Platelet count decreasedlow platelet count | 683 | 3.9% |
| Cough | 649 | 3.7% |
| Condition aggravatedthe condition being treated got worse | 648 | 3.7% |
| Malaisegeneral feeling of being unwell | 643 | 3.7% |
| White blood cell count decreasedlow white cell count | 640 | 3.7% |
| Dizzinesslight-headedness or unsteadiness | 639 | 3.7% |
| Vomitingbeing sick | 613 | 3.5% |
| Muscular weaknessmuscle weakness | 611 | 3.5% |
| Pneumonialung infection | 605 | 3.5% |
| Diarrhoealoose or frequent stools | 599 | 3.5% |
| Gait disturbancedifficulty walking | 599 | 3.5% |
| Pruritusitching | 586 | 3.4% |
| Neutropenialow neutrophils, a type of white blood cell | 577 | 3.3% |
| Insomniadifficulty sleeping | 572 | 3.3% |
| Thrombocytopenialow platelets | 561 | 3.2% |
| Chest discomfort | 557 | 3.2% |
| Hypoaesthesianumbness | 540 | 3.1% |
| Urticariahives | 523 | 3% |
| Feeling abnormalfeeling odd or not right | 502 | 2.9% |
| Pain in extremitypain in an arm or leg | 489 | 2.8% |
| Lymphopenia | 483 | 2.8% |
| Chillschills or shivering | 480 | 2.8% |
| Flushingsudden reddening or warmth of the skin | 467 | 2.7% |
| Back pain | 454 | 2.6% |
| Herpes zostershingles | 454 | 2.6% |
| Falla fall | 445 | 2.6% |
| Sepsisa severe body-wide response to infection | 444 | 2.6% |
| Tachycardiafast heart rate | 441 | 2.5% |
| Product use in unapproved indicationused for a purpose not on the label | 432 | 2.5% |
| Erythemaskin redness | 431 | 2.5% |
| Arthralgiajoint pain | 425 | 2.5% |
| Hypertensionhigh blood pressure | 417 | 2.4% |
| Contusiona bruise | 416 | 2.4% |
| Urine abnormality | 410 | 2.4% |
| Haemoglobin decreasedlow haemoglobin | 405 | 2.3% |
| Bradycardiaslow heart rate | 404 | 2.3% |
The counts add to more than 17,330 reports, because one report can record more than one term. FDA says:
No individual drug is connected to any individual reaction. When a report lists multiple drugs and multiple reactions, there is no way to conclude from the data therein that a given drug is responsible for a given reaction.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
Reports by month
FDA releases FAERS data every quarter, so the newest months are not complete. They grow in later releases.
Outcomes, patients and reporters
| Outcome | Reports | Share | Share as a bar |
|---|---|---|---|
| Death | 2,482 | 14.3% | |
| Life-threatening | 1,010 | 5.8% | |
| Hospitalization (initial or prolonged) | 5,645 | 32.6% | |
| Disability or Permanent Damage | 612 | 3.5% | |
| Congenital Anomaly/Birth Defect | 35 | 0.2% | |
| Other Serious (Important Medical Events) | 11,137 | 64.3% | |
| Not serious | 2,428 | 14% |
An outcome in a report is not proof that a drug was the cause. The reporter gives the outcome, and FDA does not verify it. A report can have more than one outcome. FDA says:
The information in these reports has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of these events.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
| Age | Reports | Share | Share as a bar |
|---|---|---|---|
| Under 2 | 413 | 2.4% | |
| 2 to 11 | 822 | 4.7% | |
| 12 to 17 | 392 | 2.3% | |
| 18 to 44 | 5,248 | 30.3% | |
| 45 to 64 | 3,874 | 22.4% | |
| 65 to 74 | 780 | 4.5% | |
| 75 and over | 294 | 1.7% | |
| Age not given | 5,507 | 31.8% |
| Reporter | Reports | Share | Share as a bar |
|---|---|---|---|
| Physician | 5,721 | 33% | |
| Pharmacist | 443 | 2.6% | |
| Other health professional | 6,907 | 39.9% | |
| Lawyer | 6 | under 0.1% | |
| Consumer or non-health professional | 3,830 | 22.1% | |
| Not given | 423 | 2.4% |
Official pages
- MedWatch Online Voluntary Reporting FormThe online form of FDA for a voluntary report.
- MedWatch: The FDA Safety Information and Adverse Event Reporting ProgramThe page of the FDA program that receives reports about drugs and devices.
- FDA Adverse Event Monitoring System (AEMS) Public DashboardThe public dashboard of FDA for adverse event reports on drugs and biologics.
The site checked these addresses on . The links open in a new tab.
Cite this page
Reported Reactions. CD52-directed cytolytic antibody: adverse event reports that FDA received. https://reportedreactions.com/class/cd52-directed-cytolytic-antibody/ Source: U.S. Food and Drug Administration, openFDA Drug Adverse Event (FAERS) files, release of . Reports received through .
Where the data come from
The counts come from the openFDA Drug Adverse Event (FAERS) bulk files, release of 1 Oct 2026. The files have the reports that FDA received through 30 Jun 2026. A drug name is the name on the report. The site matches it to a brand name or a generic name of the National Drug Code Directory of 2 Oct 2026. A class is the pharmacologic class (EPC) of the FDA label.
The class of a drug is the Established Pharmacologic Class that openFDA attaches to its reports most often. When the reports have none, it is the class in the NDC Directory. The site does not publish a report narrative, a lot number, a detail of a patient or the identity of a reporter. The record of FDA is the authority. See how the site counts reports, the data sources and the corrections page.
Questions
Which drugs are in the CD52-directed cytolytic antibody class on this site?
Alemtuzumab, Campath and Lemtrada, in order of name. The class of a drug comes from the pharmacologic class (EPC) on its FDA label.
Can the table of drugs rank the drugs?
No. FDA says:
Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
Common products may have a higher number of adverse events due to the higher total number of people using the product.
Source: openFDA, Drug Adverse Event Overview. The site read the page on .
Drugs also differ in the conditions that they treat and in their time on the market.
How does a person report an adverse event?
FDA runs MedWatch, a program that takes voluntary reports from health professionals, patients and consumers. The guide on how to report has the links.