Reports received by FDA, by month

December 2013: adverse event reports received by FDA

72,403 drug reports (FAERS) and 61,123 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.

72,403
drug reports received: 52,886 a year earlier; 62,872
monthly average, preceding 12 months: 15.2% against the average; 61,123
device reports received: 39,938 a year earlier

FDA received 72,403 drug adverse event reports in December 2013, against 52,886 in the same month a year earlier and a monthly average of 62,872 over the preceding 12 months. The MAUDE device database received 61,123 reports that month (39,938 a year earlier).

The drugs listed most often as suspect products were Tecfidera (7,361), Letairis (2,734) and Paragard 380a (2,147), and the reactions recorded most often were drug ineffective (3,699), death (3,547) and nausea (3,513).

Relative to their own average over the preceding 12 months, the drugs whose report count rose most were Picato (77.7× its average), Atripla (22.5× its average) and Thalomid (19.6× 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 December 2013

Drugs listed most often as suspect products

Drug	Reports	Share of the month
Tecfidera	7,361	10.2%
Letairis	2,734	3.8%
Paragard 380a	2,147	3%
Dianeal Low Calcium	1,790	2.5%
Enbrel	1,649	2.3%
Tysabri	1,420	2%
Picato	1,295	1.8%
Revlimid	1,008	1.4%
Avonex	992	1.4%
Humira	964	1.3%
Votrient	798	1.1%
Mirena	789	1.1%
Lyrica	749	1%
Nicoderm Cq Clear 21mg	684	0.9%
Remicade	618	0.9%

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
Picato	1,295	77.7×
Atripla	264	22.5×
Thalomid	597	19.6×
Ranexa	233	17.9×
Claritin-D-24	211	15.6×
Metoclopramide hydrochloride	174	14.8×
Perjeta	179	13.7×
Tecfidera	7,361	12.7×

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
Drug ineffectivethe medicine did not work as expected	3,699	5.1%
Deaththe patient died; cause not stated by this term	3,547	4.9%
Nauseafeeling sick	3,513	4.9%
Diarrhoealoose or frequent stools	2,821	3.9%
Fatiguetiredness	2,584	3.6%
Headachehead pain	2,231	3.1%
Flushingsudden reddening or warmth of the skin	2,221	3.1%
Dyspnoeashortness of breath	2,213	3.1%
Vomitingbeing sick	2,153	3%
Dizzinesslight-headedness or unsteadiness	1,863	2.6%
Painpain, site not specified	1,757	2.4%
Malaisegeneral feeling of being unwell	1,677	2.3%
Pruritusitching	1,602	2.2%
Off label useused for a purpose or in a way not on the label	1,471	2%
Rashskin rash	1,452	2%

Devices named most often

Brand	Reports	Share of device reports
Spectrum Infusion Pump	5,182	8.5%
Onetouchping Glucosemgmtsystem	2,165	3.5%
Ot Verio Iq Meter	1,293	2.1%
Capsurefix Novus	741	1.2%
HomeChoice Automated PD Set with Cassette	651	1.1%
Paradigm Real-Time Revel Insulin Infusion Pump	607	1%
Animas Insulin Infusion Pump	545	0.9%
Gynecare Tvt Obturator System	516	0.8%
Gynecare Tvt Retropubic System	512	0.8%
Paradigm Real-Time Insulin Infusion Pump	484	0.8%

Questions about December 2013

How many adverse event reports did FDA receive in December 2013?

72,403 drug reports are in the openFDA FAERS release of 28 Sep 2026, and 61,123 device reports in the MAUDE release of 28 Sep 2026. The same month a year earlier has 52,886 drug reports.

Which drugs were listed most often?

Tecfidera (7,361), Letairis (2,734), Paragard 380a (2,147), Dianeal Low Calcium (1,790) and Enbrel (1,649).

Which reactions were recorded most often?

drug ineffective (3,699), death (3,547), nausea (3,513), diarrhoea (2,821) and fatigue (2,584).

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.