Reports received by FDA, by month

April 2010: adverse event reports received by FDA

30,845 drug reports (FAERS) and 20,867 device reports (MAUDE).

Read first · FDA's statement on these data

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. openFDA, FDA

FDA adds: "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 "cannot be used to estimate the incidence of these events."

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.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

30,845
drug reports received: 25,716 a year earlier; 29,757
monthly average, preceding 12 months: 3.7% against the average; 20,867
device reports received: 17,946 a year earlier

FDA received 30,845 drug adverse event reports in April 2010, against 25,716 in the same month a year earlier and a monthly average of 29,757 over the preceding 12 months. The MAUDE device database received 20,867 reports that month (17,946 a year earlier).

The drugs listed most often as suspect products were Tysabri (2,245), Avonex (864) and Avandia (526), and the reactions recorded most often were nausea (1,228), death (1,184) and fatigue (1,150).

Relative to their own average over the preceding 12 months, the drugs whose report count rose most were Toprol-Xl (12.1× its average), Latisse (8.1× its average) and Solostar (6.7× its average). A jump in one month usually reflects a batch of reports from a manufacturer, a publicised event or a new product, not a change in what happens to patients.

Drug reports by month, three years to April 2010

Drugs listed most often as suspect products

Drug	Reports	Share of the month
Tysabri	2,245	7.3%
Avonex	864	2.8%
Avandia	526	1.7%
Latisse	470	1.5%
Remicade	463	1.5%
Tiotropium bromide	440	1.4%
Humira	420	1.4%
Nexium	385	1.2%
Forteo	375	1.2%
Revlimid	361	1.2%
Dianeal	327	1.1%
Soliris	324	1.1%
Toprol-Xl	312	1%
Seroquel	307	1%
Enbrel	304	1%

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."

Largest rises against their own average

Drug	Reports this month	Times its 12-month average
Toprol-Xl	312	12.1×
Latisse	470	8.1×
Solostar	174	6.7×
Tysabri	2,245	6.3×
Metoprolol succinate	108	6.1×
Tocilizumab	55	5.4×
Tenormin	58	5.4×
Sensipar	71	5.3×

Drugs with at least 50 reports in the month and an average of at least 10 a month over the preceding year. A rise usually reflects a batch of manufacturer reports, a publicised event or a new product.

Reactions recorded most often

MedDRA term	Reports	Share of the month
Nauseafeeling sick	1,228	4%
Deaththe patient died; cause not stated by this term	1,184	3.8%
Fatiguetiredness	1,150	3.7%
Drug ineffectivethe medicine did not work as expected	1,133	3.7%
Dyspnoeashortness of breath	1,113	3.6%
Headachehead pain	1,019	3.3%
Diarrhoealoose or frequent stools	937	3%
Vomitingbeing sick	929	3%
Dizzinesslight-headedness or unsteadiness	853	2.8%
Astheniaweakness or lack of energy	830	2.7%
Pyrexiafever	811	2.6%
Painpain, site not specified	740	2.4%
Falla fall	714	2.3%
Malaisegeneral feeling of being unwell	694	2.2%
Pneumonialung infection	648	2.1%

Devices named most often

Brand	Reports	Share of device reports
One Touch Ultralink Meter	371	1.8%
One Touch Ping Meter	366	1.8%
Constellation With Laser	192	0.9%
Precision?	178	0.9%
M Series	170	0.8%
Accu-Chek Spirit	158	0.8%
Totalcare	155	0.7%
Centra 850 Bed Centra Bed 3 Motor	148	0.7%
Accu-Chek Aviva Test Strips	140	0.7%
Perclose Proglide 6f Suture Mediated Closure Smc System	136	0.7%

Questions about April 2010

How many adverse event reports did FDA receive in April 2010?

30,845 drug reports are in the openFDA FAERS release of 28 Sep 2026, and 20,867 device reports in the MAUDE release of 28 Sep 2026. The same month a year earlier has 25,716 drug reports.

Which drugs were listed most often?

Tysabri (2,245), Avonex (864), Avandia (526), Latisse (470) and Remicade (463).

Which reactions were recorded most often?

nausea (1,228), death (1,184), fatigue (1,150), drug ineffective (1,133) and dyspnoea (1,113).

Can the count for a month still change?

Yes. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Older months change little.

Does a busy month mean something happened that month?

Not by itself. The date is when FDA received the report, not when the event occurred, and volume follows manufacturer batches, product launches and publicity. 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."

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. 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.