FDA label 42031ffa-8a7c-48f9-a16a-19d86985d89c
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- 109edaaf-f13c-4d4c-aa40-0f9058379158
- SPL ID
- 42031ffa-8a7c-48f9-a16a-19d86985d89c
- Version
- 9
- Effective date
- 2016-07-27
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:29:33
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | 42031ffa-8a7c-48f9-a16a-19d86985d89c | id | |
| spl set id | 109edaaf-f13c-4d4c-aa40-0f9058379158 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS Myocardial ischemia/infarction and Prinzmetal's angina: Perform cardiac evaluation in patients with multiple cardiovascular risk factors. ( 5.1 ) Arrhythmias: Discontinue ALSUMA if occurs. ( 5.2 ) Chest/throat/neck/jaw pain, tightness, pressure, or heaviness: Generally not associated with myocardial ischemia; evaluate for coronary artery disease in patients at high risk. ( 5.3 ) Cerebral hemorrhage, subarachnoid hemorrhage, and stroke: Discontinue ALSUMA if occurs. ( 5.4 ) Gastrointestinal ischemia and infarction events, peripheral vasospastic reactions. Discontinue ALSUMA if occurs. ( 5.5 ) Medication overuse headache: Detoxification may be necessary. ( 5.6 ) Serotonin syndrome: Discontinue ALSUMA if occurs. ( 5.7 ) Seizures: Use with caution if patients with epilepsy or a lowered seizure threshold. ( 5.10 ) 5.1 Myocardial Ischemia, Myocardial Infarction, and Prinzmetal's Angina ALSUMA is contraindicated in patients with ischemic or vasospastic CAD. There have been rare reports of serious cardiac adverse reactions, including acute myocardial infarction, occurring within a few hours following administration of sumatriptan. Some of these reactions occurred in patients without known CAD. ALSUMA may cause coronary artery vasospasm (Prinzmetal's angina), even in patients without a history of CAD. Perform a cardiovascular evaluation in triptan-naive patients who have multiple cardiovascular risk factors (e.g., increased age, diabetes, hypertension, smoking, obesity, strong family history of CAD) prior to receiving ALSUMA. If there is evidence of CAD or coronary artery vasospasm, ALSUMA is contraindicated. For patients with multiple cardiovascular risk factors who have a negative cardiovascular evaluation, consider administering the first dose of ALSUMA in a medically supervised setting and performing an electrocardiogram (ECG) immediately following ALSUMA. For such patients, consider periodic cardiovascular evaluation in intermittent long-term users of ALSUMA. 5.2 Arrhythmias Life-threatening disturbances of cardiac rhythm, including ventricular tachycardia and ventricular fibrillation leading to death, have been reported within a few hours following the administration of 5-HT 1 agonists. Discontinue ALSUMA if these disturbances occur. ALSUMA is contraindicated in patients with Wolff-Parkinson-White syndrome or arrhythmias associated with other cardiac accessory conduction pathway disorders. 5.3 Chest, Throat, Neck and/or Jaw Pain/Tightness/Pressure Sensations of tightness, pain, pressure, and heaviness in the precordium, throat, neck, and jaw commonly occur after treatment with ALSUMA and are usually non-cardiac in origin. However, perform a cardiac evaluation if these patients are at high cardiac risk. The use of ALSUMA is contraindicated in patients shown to have CAD and those with Prinzmetal's variant angina. 5.4 Cerebrovascular Events Cerebral hemorrhage, subarachnoid hemorrhage, and stroke have occurred in patients treated with 5-HT 1 agonists, and some have resulted in fatalities. In a number of cases, it appears possible that the cerebrovascular events were primary, the 5-HT 1 agonists having been administered in the incorrect belief that the symptoms experienced were a consequence of migraine when they were not. Also, patients with migraine may be at increased risk of certain cerebrovascular events (e.g., stroke, hemorrhage, TIA). Discontinue ALSUMA if a cerebrovascular event occurs. Before treating headaches in patients not previously diagnosed as migraineurs, and in migraineurs who present with atypical symptoms, exclude other potentially serious neurological conditions. ALSUMA is contraindicated in patients with a history of stroke or TIA. 5.5 Other Vasospasm Reactions ALSUMA may cause non-coronary vasospastic reactions, such as peripheral vascular ischemia, gastrointestinal vascular ischemia and infarction (presenting with abdominal pain and bloody diarrhea), splenic infarction, and Raynaud's syndrome. In patients who experience symptoms or signs suggestive of non-coronary vasospasm reaction following the use of any 5-HT 1 agonist, rule out a vasospastic reaction before receiving additional ALSUMA doses. Reports of transient and permanent blindness and significant partial vision loss have been reported with the use of 5-HT 1 agonists. Since visual disorders may be part of a migraine attack, a causal relationship between these events and the use of 5-HT 1 agonists have not been clearly established. 5.6 Medication Overuse Headache Overuse of acute migraine drugs (e.g., ergotamine, triptans, opioids, or combination of these drugs for 10 or more days per month) may lead to exacerbation of headache (medication overuse headache). Medication overuse headache may present as migraine-like daily headaches or as a marked increase in frequency of migraine attacks. Detoxification of patients, including withdrawal of the overused drugs and treatment of withdrawal symptoms (which often includes a transient worsening of headache) may be necessary. 5.7 Serotonin Syndrome Serotonin syndrome may occur with ALSUMA, particularly during co-administration with selective serotonin reuptake inhibitors (SSRIs), serotonin norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), and MAO inhibitors [see Drug Interactions (7.4) ] . Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular aberrations (e.g., hyperreflexia, incoordination), and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). The onset of symptoms usually occurs within minutes to hours of receiving a new or a greater dose of a serotonergic medication. Discontinue ALSUMA if serotonin syndrome is suspected. 5.8 Increase in Blood Pressure Significant elevation in blood pressure, including hypertensive crisis with acute impairment of organ systems, has been reported on rare occasions in patients treated with 5-HT 1 agonists, including patients without a history of hypertension. Monitor blood pressure in patients treated with ALSUMA. ALSUMA is contraindicated in patients with uncontrolled hypertension. 5.9 Anaphylactic/Anaphylactoid Reactions There have been reports of anaphylactic, anaphylactoid, and hypersensitivity reactions including angioedema in patients receiving ALSUMA. Such reactions can be life threatening or fatal. In general, anaphylactic reactions to drugs are more likely to occur in individuals with a history of sensitivity to multiple allergens. ALSUMA is contraindicated in patients with a history of hypersensitivity reaction to ALSUMA. 5.10 Seizures Seizures have been reported following administration of ALSUMA. Some have occurred in patients with either a history of seizures or concurrent conditions predisposing to seizures. There are also reports in patients where no such predisposing factors are apparent. ALSUMA should be used with caution in patients with a history of epilepsy or conditions associated with a lowered seizure threshold.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS The following adverse reactions are discussed in more detail in other sections of the prescribing information: 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 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 Pfizer Inc. at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 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 subjects [ Studies 2 and 3, see Clinical Studies (14.1) ] 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 Reported by at Least 2% of Subjects and at a Greater Frequency Than Placebo in 2 Placebo-Controlled Migraine Clinical Trials (Studies 2 and 3) The sum of the percentages cited is greater than 100% because subjects may have experienced more than 1 type of adverse reaction. Only reactions that occurred at a frequency of 2% or more in groups treated with sumatriptan injection and occurred at a frequency greater than the placebo groups are included. Percent of Subjects Reporting Adverse Reaction Sumatriptan 6 mg Subcutaneous (n = 547) Placebo (n = 370) Atypical sensations 42 9 Tingling 14 3 Warm/hot sensation 11 4 Burning sensation 7 <1 Feeling of heaviness 7 1 Pressure sensation 7 2 Feeling of tightness 5 <1 Numbness 5 2 Feeling strange 2 <1 Tight feeling in head 2 <1 Cardiovascular Flushing 7 2 Chest Discomfort 5 1 Tightness in chest 3 <1 Pressure in chest 2 <1 Ear, nose and throat Throat discomfort 3 <1 Discomfort: nasal cavity/sinuses 2 <1 Injection site reaction Includes injection site pain, stinging/burning, swelling, erythema, bruising, bleeding. 59 24 Miscellaneous Jaw discomfort 2 0 Musculoskeletal Weakness 5 <1 Neck pain/stiffness 5 <1 Myalgia 2 <1 Neurological Dizziness/vertigo 12 4 Drowsiness/sedation 3 2 Headache 2 <1 Skin Sweating 2 1 The incidence of adverse reactions in controlled clinical trials was not affected by gender or age of the subjects. 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, see Clinical Studies (14.2) ] , no new significant adverse reactions were detected that had not already been identified in trials of sumatriptan in subjects 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, 0% placebo), nausea and vomiting (4% sumatriptan, 0% placebo), and bronchospasm (1% sumatriptan, 0% placebo). Adverse Reactions Observed In Association With The Administration of ALSUMA: The safety of ALSUMA was evaluated in an open-label clinical trial evaluating the usability of ALSUMA during a migraine attack. Adverse reactions that occurred at a frequency of 5% or higher were injection site bruising (16%), injection site pain (6%), and injection site hemorrhage (6%).
adverse reactions table
<table width="75%" ID="table1"> <caption>Table 1. Adverse Reactions Reported by at Least 2% of Subjects and at a Greater Frequency Than Placebo in 2 Placebo-Controlled Migraine Clinical Trials (Studies 2 and 3)<footnote>The sum of the percentages cited is greater than 100% because subjects may have experienced more than 1 type of adverse reaction. Only reactions that occurred at a frequency of 2% or more in groups treated with sumatriptan injection and occurred at a frequency greater than the placebo groups are included.</footnote> </caption> <col width="25%" align="left" valign="top"/> <col width="37%" align="center" valign="top"/> <col width="38%" align="center" valign="top"/> <thead> <tr> <th styleCode="Lrule Rrule"/> <th styleCode="Botrule Rrule" colspan="2">Percent of Subjects Reporting</th> </tr> <tr> <th styleCode="Lrule Rrule" align="center" valign="bottom">Adverse Reaction</th> <th styleCode="Rrule">Sumatriptan 6 mg Subcutaneous (n = 547)</th> <th styleCode="Rrule">Placebo (n = 370)</th> </tr> </thead> <tbody> <tr> <td styleCode="Lrule Rrule">Atypical sensations</td> <td styleCode="Rrule">42</td> <td styleCode="Rrule">9</td> </tr> <tr> <td styleCode="Lrule Rrule"> Tingling</td> <td styleCode="Rrule">14</td> <td styleCode="Rrule">3</td> </tr> <tr> <td styleCode="Lrule Rrule"> Warm/hot sensation</td> <td styleCode="Rrule">11</td> <td styleCode="Rrule">4</td> </tr> <tr> <td styleCode="Lrule Rrule"> Burning sensation</td> <td styleCode="Rrule">7</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule"> Feeling of heaviness</td> <td styleCode="Rrule">7</td> <td styleCode="Rrule">1</td> </tr> <tr> <td styleCode="Lrule Rrule"> Pressure sensation</td> <td styleCode="Rrule">7</td> <td styleCode="Rrule">2</td> </tr> <tr> <td styleCode="Lrule Rrule"> Feeling of tightness</td> <td styleCode="Rrule">5</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule"> Numbness</td> <td styleCode="Rrule">5</td> <td styleCode="Rrule">2</td> </tr> <tr> <td styleCode="Lrule Rrule"> Feeling strange</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Tight feeling in head</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule">Cardiovascular</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Flushing</td> <td styleCode="Rrule">7</td> <td styleCode="Rrule">2</td> </tr> <tr> <td styleCode="Lrule Rrule">Chest Discomfort</td> <td styleCode="Rrule">5</td> <td styleCode="Rrule">1</td> </tr> <tr> <td styleCode="Lrule Rrule"> Tightness in chest</td> <td styleCode="Rrule">3</td> <td styleCode="Rrule"><1</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Pressure in chest</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule">Ear, nose and throat</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr> <td styleCode="Lrule Rrule"> Throat discomfort</td> <td styleCode="Rrule">3</td> <td styleCode="Rrule"><1</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Discomfort: nasal cavity/sinuses</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule">Injection site reaction<footnote>Includes injection site pain, stinging/burning, swelling, erythema, bruising, bleeding.</footnote> </td> <td styleCode="Rrule">59</td> <td styleCode="Rrule">24</td> </tr> <tr> <td styleCode="Lrule Rrule">Miscellaneous</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Jaw discomfort</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule">0</td> </tr> <tr> <td styleCode="Lrule Rrule">Musculoskeletal</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr> <td styleCode="Lrule Rrule"> Weakness</td> <td styleCode="Rrule">5</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule"> Neck pain/stiffness</td> <td styleCode="Rrule">5</td> <td styleCode="Rrule"><1</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Myalgia</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule">Neurological</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr> <td styleCode="Lrule Rrule"> Dizziness/vertigo</td> <td styleCode="Rrule">12</td> <td styleCode="Rrule">4</td> </tr> <tr> <td styleCode="Lrule Rrule"> Drowsiness/sedation</td> <td styleCode="Rrule">3</td> <td styleCode="Rrule">2</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Headache</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule"><1</td> </tr> <tr> <td styleCode="Lrule Rrule">Skin</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr> <td styleCode="Lrule Rrule"> Sweating</td> <td styleCode="Rrule">2</td> <td styleCode="Rrule">1</td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.