FDA label 4d670f5c-7719-4e68-8a96-dcd26421d29c

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SPL set ID
9324e2eb-26fd-4f14-9f10-e5aa467306f4
SPL ID
4d670f5c-7719-4e68-8a96-dcd26421d29c
Version
11
Effective date
2022-09-27
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:53

Warnings cross-check#

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warnings and cautions

5 WARNINGS AND PRECAUTIONS Life-threatening paradoxical bronchospasm may occur. Discontinue PROAIR RESPICLICK immediately and treat with alternative therapy. ( 5.1 ) Need for more doses of PROAIR RESPICLICK than usual may be a sign of deterioration of asthma and requires reevaluation of treatment. ( 5.2 ) PROAIR RESPICLICK is not a substitute for corticosteroids. ( 5.3 ) Cardiovascular effects may occur. Use with caution in patients sensitive to sympathomimetic drugs and patients with cardiovascular or convulsive disorders. ( 5.4 , 5.7 ) Excessive use may be fatal. Do not exceed recommended dose. ( 5.5 ) Immediate hypersensitivity reactions may occur. Discontinue PROAIR RESPICLICK immediately. ( 5.6 ) Hypokalemia and changes in blood glucose may occur. ( 5.7 , 5.8 ) 5.1 Paradoxical Bronchospasm PROAIR RESPICLICK can produce paradoxical bronchospasm that may be life threatening. If paradoxical bronchospasm occurs, PROAIR RESPICLICK should be discontinued immediately and alternative therapy instituted. 5.2 Deterioration of Asthma Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of PROAIR RESPICLICK, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, eg, corticosteroids. 5.3 Use of Anti-Inflammatory Agents The use of beta-adrenergic-agonist bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents, e.g., corticosteroids, to the therapeutic regimen. 5.4 Cardiovascular Effects PROAIR RESPICLICK, like other beta-adrenergic agonists, can produce clinically significant cardiovascular effects in some patients as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon after administration of PROAIR RESPICLICK at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce ECG changes, such as flattening of the T-wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, PROAIR RESPICLICK, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension. 5.5 Do Not Exceed Recommended Dose Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs in patients with asthma. The exact cause of death is unknown, but cardiac arrest following an unexpected development of a severe acute asthmatic crisis and subsequent hypoxia is suspected. 5.6 Hypersensitivity Reactions including Anaphylaxis Immediate hypersensitivity reactions may occur after administration of albuterol sulfate, as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, anaphylaxis, and oropharyngeal edema. PROAIR RESPICLICK contains small amounts of lactose, which may contain trace levels of milk proteins. Hypersensitivity reactions including anaphylaxis, angioedema, pruritus, and rash have been reported with the use of therapies containing lactose (lactose is an inactive ingredient in PROAIR RESPICLICK). The potential for hypersensitivity must be considered in the clinical evaluation of patients who experience immediate hypersensitivity reactions while receiving PROAIR RESPICLICK. 5.7 Coexisting Conditions PROAIR RESPICLICK, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension; in patients with convulsive disorders, hyperthyroidism, or diabetes mellitus; and in patients who are unusually responsive to sympathomimetic amines. Clinically significant changes in systolic and diastolic blood pressure have been seen in individual patients and could be expected to occur in some patients after use of any beta-adrenergic bronchodilator. Large doses of intravenous albuterol have been reported to aggravate preexisting diabetes mellitus and ketoacidosis. 5.8 Hypokalemia As with other beta-agonists, PROAIR RESPICLICK may produce significant hypokalemia in some patients, possibly through intracellular shunting, which has the potential to produce adverse cardiovascular effects. The decrease is usually transient, not requiring supplementation.

Adverse reactions cross-check#

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adverse reactions

6 ADVERSE REACTIONS Use of PROAIR RESPICLICK may be associated with the following: Paradoxical bronchospasm [see Warnings and Precautions ( 5.1 )] Cardiovascular Effects [see Warnings and Precautions ( 5.4 )] Immediate hypersensitivity reactions [see Warnings and Precautions ( 5.6 )] Hypokalemia [see Warnings and Precautions ( 5.8 ) Most common adverse reactions (≥1% and >placebo) are back pain, pain, gastroenteritis viral, sinus headache, urinary tract infection, nasopharyngitis, oropharyngeal pain and vomiting. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Teva Respiratory, LLC at 1-888-482-9522 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience A total of 1289 subjects were treated with PROAIR RESPICLICK during the clinical development program. The most common adverse reactions (≥1% and > placebo) were back pain, pain, gastroenteritis viral, sinus headache, and urinary tract infection. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Adults and Adolescents 12 years of Age and Older : The adverse reaction information presented in Table 1 below concerning PROAIR RESPICLICK is derived from the 12-week blinded treatment period of three studies which compared PROAIR RESPICLICK 180 mcg four times daily with a double-blinded matched placebo in 653 asthmatic patients 12 to 76 years of age. Table 1: Adverse Reactions Experienced by Greater Than or Equal to 1.0% of Adult and Adolescent Patients in the PROAIR RESPICLICK Group and Greater Than Placebo in three 12-Week Clinical Trials 1 Preferred Term Number (%) of patients PROAIR RESPICLICK 180 mcg QID N=321 Placebo N=333 Back pain 6 (2%) 4 (1%) Pain 5 (2%) 2 (<1%) Gastroenteritis viral 4 (1%) 3 (<1%) Sinus headache 4 (1%) 3 (<1%) Urinary tract infection 4 (1%) 3 (<1%) 1. This table includes all adverse events (whether considered by the investigator drug related or unrelated to drug) which occurred at an incidence rate of greater than or equal to 1.0% in the PROAIR RESPICLICK group and greater than placebo. In a long-term study of 168 patients treated with PROAIR RESPICLICK for up to 52 weeks (including a 12-week double-blind period), the most commonly reported adverse events greater than or equal to 5% were upper respiratory infection, nasopharyngitis, sinusitis, bronchitis, cough, oropharyngeal pain, headache, and pyrexia. In a small cumulative dose study, tremor, palpitations, and headache were the most frequently occurring (≥5%) adverse events. Pediatric Patients 4 to 11 Years of Age : The adverse reaction information presented in Table 2 below concerning PROAIR RESPICLICK is derived from a 3‑week pediatric clinical trial which compared PROAIR RESPICLICK 180 mcg albuterol 4 times daily with a double‑blinded matched placebo in 185 asthmatic patients 4 to 11 years of age. Table 2: Adverse Reactions Experienced by Greater Than or Equal to 2.0% of Patients 4 to 11 Years of Age in the PROAIR RESPICLICK Group and Greater Than Placebo in the 3 Week Trial Preferred Term Number (%) of patients PROAIR RESPICLICK 180 mcg QID N=93 Placebo N=92 Nasopharyngitis 2 (2%) 1 (1%) Oropharyngeal pain 2 (2%) 1 (1%) Vomiting 3 (3%) 1 (1%) 6.2 Postmarketing Experience In addition to the adverse reactions reported from clinical trials with PROAIR RESPICLICK, the following adverse events have been reported during use of other inhaled albuterol sulfate products: Urticaria, angioedema, rash, bronchospasm, hoarseness, oropharyngeal edema, and arrhythmias (including atrial fibrillation, supraventricular tachycardia, extrasystoles), rare cases of aggravated bronchospasm, lack of efficacy, asthma exacerbation (potentially fatal), muscle cramps, and various oropharyngeal side-effects such as throat irritation, altered taste, glossitis, tongue ulceration, and gagging. 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. In addition, albuterol, like other sympathomimetic agents, can cause adverse reactions such as: angina, hypertension or hypotension, palpitations, central nervous system stimulation, insomnia, headache, nervousness, tremor, muscle cramps, drying or irritation of the oropharynx, hypokalemia, hyperglycemia, and metabolic acidosis.

adverse reactions table

<table><col/><col/><col/><thead><tr><th styleCode=" Botrule Toprule Lrule Rrule" rowspan="2"><content styleCode="bold">Preferred Term</content></th><th styleCode=" Botrule Toprule Rrule" colspan="2"><content styleCode="bold">Number (%) of patients</content></th></tr><tr><th align="center" styleCode=" Botrule Rrule"><content styleCode="bold">PROAIR RESPICLICK 180 mcg QID</content> <content styleCode="bold">N=321</content></th><th align="center" styleCode=" Botrule Rrule"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=333</content></th></tr></thead><tbody><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Back pain</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>6 (2%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>4 (1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Pain</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>5 (2%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>2 (&lt;1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Gastroenteritis viral</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>4 (1%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>3 (&lt;1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Sinus headache</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>4 (1%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>3 (&lt;1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Urinary tract infection</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>4 (1%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>3 (&lt;1%)</paragraph></td></tr></tbody></table>

adverse reactions table

<table><col/><col/><col/><thead><tr><th styleCode=" Botrule Toprule Lrule Rrule" rowspan="2"><content styleCode="bold">Preferred Term</content></th><th styleCode=" Botrule Toprule Rrule" colspan="2"><content styleCode="bold">Number (%) of patients</content></th></tr><tr><th align="center" styleCode=" Botrule Rrule"><content styleCode="bold">PROAIR RESPICLICK 180 mcg QID</content> <content styleCode="bold">N=93</content></th><th align="center" styleCode=" Botrule Rrule"><content styleCode="bold">Placebo</content> <content styleCode="bold">N=92</content></th></tr></thead><tbody><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Nasopharyngitis</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>2 (2%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>1 (1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Oropharyngeal pain</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>2 (2%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>1 (1%)</paragraph></td></tr><tr><td styleCode=" Botrule Lrule Rrule"><paragraph>Vomiting</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>3 (3%)</paragraph></td><td align="center" styleCode=" Botrule Rrule"><paragraph>1 (1%)</paragraph></td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.