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Published: December 2011

Dabigatran etexilate (Pradaxa): Summary of reports to CARM

Prescriber Update 32(4): 29-30
December 2011

The funding of Pradaxa by Pharmac on 1 July 2011 has created a great deal of interest among healthcare professionals and the public. In turn this has stimulated the reporting of suspected adverse reactions associated with Pradaxa to the Centre for Adverse Reactions Monitoring (CARM).

Early data indicates that about 10,000 patients started dabigatran treatment up until the end of September 2011.

As of 7 November 2011 there were 295 reports in the CARM database detailing suspected adverse reactions to dabigatran. These reports were distributed across the different body systems as outlined in table 1. A suspected adverse reaction does not necessarily mean that the medicine caused the reaction, merely that the reporter suspected it may have.

Table 1: Distribution of reported suspected reactions to dabigatran

Category# Total number of reactions*
Alimentary 256
Application site 1
Cardiovascular 41
Endocrine/Metabolic 8
Haematological 27
Musculoskeletal 14
Nervous System 37
Other 28
Procedure Related 20
Product Related 2
Psychiatric Changes 35
Reproductive disorders 1
Resistance Mechanism Disorders 2
Respiratory 31
Skin & appendages 28
Special Senses 3
Urinary 28

# CARM classification

* The number of reactions is greater than the number of reports as one report may include one or more suspected reactions.

Gastrointestinal reactions were the most common adverse events reported. These reports (excluding cases of bleeds) accounted for 42% of all reports (124/295). The majority of reactions reported were considered non-serious by CARM and may be expected based on clinical data provided in the report, in addition to being described in the data sheet.

The eleven most commonly reported suspected adverse reactions are outlined in Table 2 on page 30.

There were a total of 20 medication errors reported to CARM. These reports generally described cases where the patient was either incorrectly switched from warfarin, given the incorrect dose for their age, or should not have been treated with dabigatran at all, such as those with severe renal impairment. The majority of these reports were received within the first few weeks of funding. Since the beginning of October only two reports of medication error were received.

Of the 295 reports, 78 (26%) were considered serious by CARM, as detailed in Figure 1.

Figure 1: Dabigatran serious reports
Figure 1 Pie Chart Key Figure 1 Patient hospitalised 55
Key Figure 1 Patient died 10
Key Figure 1 Intervention required 3
Key Figure 1 Life threatening 9
Key Figure 1 Persisting disability 1

Table 2: Most commonly reported suspected adverse reactions to dabigatran

Adverse event Number Category
Dyspepsia 60 Alimentary
Rectal bleeding 47 Alimentary
Diarrhoea 26 Alimentary
Melaena 24 Alimentary
Medication error 20 Procedure Related
Abdominal pain 19 Alimentary
Haematuria 17 Urinary
Headache 14 Nervous System
Gastroesophageal reflux 13 Alimentary
GI haemorrhage 13 Alimentary
Dyspnoea 13 Alimentary

CARM considered that in all of the fatal cases received up to 7 November 2011, the death was unrelated to treatment with dabigatran. In these cases the death was attributed to another medicine or unrelated event such as pneumonia.

Adverse reaction data indicates that bleeding is the most important risk associated with dabigatran, specifically:

Medsafe has reviewed the incidence of adverse reactions in elderly patients. To date the data indicates there is a slightly higher incidence of reports of suspected adverse reactions in patients aged 80 years and above. Medsafe continues to closely monitor the safety of dabigatran in older patients.

When assessing the risks associated with dabigatran, an obvious medicine to compare it with is warfarin. A comparison using spontaneous adverse reaction reports is not strictly advisable due to the length of time warfarin has been available and the stimulated reporting of suspected adverse reactions to dabigatran. However, a crude comparison does provide some context for readers.

In the period between 1 Jan 2006 and 31 Dec 2010, CARM received 127 adverse reaction reports for warfarin. Sixty-five percent of these reports were considered to be serious, including 15 fatal reports. Of these fatal reports, CARM considered that warfarin had contributed to the patient’s death in 11 cases.

The global number of adverse reaction describing serious bleeds, including New Zealand data, is noted to be lower than that seen in the clinical studies published to date. Healthcare professionals are reminded that all anticoagulants have risks including the risk of bleeding, and patients taking these medicines should be closely monitored for signs of bleeding.

Please continue to report all suspected adverse reactions to any anticoagulant to CARM.


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