Sumatriptan - Side Effects sumatriptan succinate

Side Effects for SUMATRIPTAN (sumatriptan succinate injection) are also known as adverse reactions. Below is a summary of known side effects for Sumatriptan. If you experience side effects when taking Sumatriptan, be sure to tell your doctor.

Adverse Reactions

The following serious adverse reactions are described below and elsewhere in the labeling:

  • Myocardial ischemia, myocardial infarction, and Prinzmetal's angina [see Warnings and Precautions (5.1)]
  • Arrhythmias [see Warnings and Precautions (5.2)]
  • Chest, throat, neck, and/or jaw pain/tightness/pressure [see Warnings and Precautions (5.3)]
  • Cerebrovascular events [see Warnings and Precautions (5.4)]
  • Other vasospasm reactions [see Warnings and Precautions (5.5)]
  • Medication overuse headache [see Warnings and Precautions (5.6)]
  • Serotonin syndrome [see Warnings and Precautions (5.7)]
  • Increase in blood pressure [see Warnings and Precautions (5.8)]
  • Hypersensitivity reactions [see Contraindications (4), Warnings and Precautions (5.9)]
  • Seizures [see Warnings and Precautions (5.10)]

Most common adverse reactions (≥5% and > placebo) were injection site reactions, tingling, dizziness/vertigo, warm/hot sensation, burning sensation, feeling of heaviness, pressure sensation, flushing, feeling of tightness, and numbness (6.1)

To report SUSPECTED ADVERSE REACTIONS, contact Antares Pharma, Inc. at 1-855-287-7476 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

clinical trials experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in practice.

Migraine Headache

Table 1 lists adverse reactions that occurred in 2 US placebo-controlled clinical trials in migraine patients (Studies 2 and 3) following either a single 6 mg dose of sumatriptan injection or placebo. Only reactions that occurred at a frequency of 2% or more in groups treated with sumatriptan injection 6 mg and that occurred at a frequency greater than the placebo group are included in Table 1.

Table 1. Adverse Reactions in Pooled Placebo-Controlled Trials in Patients with Migraine (Studies 2 and 3)

a Includes injection site pain, stinging/burning, swelling, erythema, bruising, bleeding.


Sumatriptan Injection
6 mg Subcutaneous
(n = 547)
%
Placebo
(n = 370)
%
Atypical sensations
    Tingling
    Warm/hot sensation
    Burning sensation
    Feeling of heaviness
    Pressure sensation
    Feeling of tightness
    Numbness
    Feeling strange
    Tight feeling in head
42
14
11
7
7
7
5
5
2
2
9
3
4
<1
1
2
<1
2
<1
<1
Cardiovascular
    Flushing
    Chest discomfort
    Tightness in chest
    Pressure in chest

7
5
3
2

2
1
<1
<1
Ear, nose, and throat
    Throat discomfort
    Discomfort: nasal cavity/sinuses

3
2

<1
<1
Injection site reactiona 59 24
Miscellaneous
    Jaw discomfort

2

0
Musculoskeletal
    Weakness
    Neck pain/stiffness
    Myalgia

5
5
2

<1
<1
<1
Neurological
    Dizziness/vertigo
    Drowsiness/sedation
    Headache

12
3
2

4
2
<1
Skin
    Sweating

2

1

The incidence of adverse reactions in controlled clinical trials was not affected by gender or age of the patients. There were insufficient data to assess the impact of race on the incidence of adverse reactions.

Cluster Headache

In the controlled clinical trials assessing the efficacy of sumatriptan injection as a treatment for cluster headache (Studies 4 and 5), no new significant adverse reactions were detected that had not already been identified in trials of sumatriptan injection in patients with migraine.

Overall, the frequency of adverse reactions reported in the trials of cluster headache was generally lower than in the migraine trials. Exceptions include reports of paresthesia (5% sumatriptan injection, 0% placebo), nausea and vomiting (4% sumatriptan injection, 0% placebo), and bronchospasm (1% sumatriptan injection, 0% placebo).

postmarketing experience

The following adverse reactions have been identified during postapproval use of sumatriptan tablets, sumatriptan nasal spray, and sumatriptan injection. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Cardiovascular

Hypotension, palpitations.

Neurological

Dystonia, tremor.

This drug label information is as submitted to the Food and Drug Administration (FDA) and is intended for informational purposes only. If you think you may have a medical emergency, immediately call your doctor or dial 911. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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