Phenergan is a well-known brand of promethazine, a sedating antihistamine used for allergy relief, motion sickness, nausea and vomiting, and short-term nighttime sedation. Because it works on both histamine and the brain’s nausea centers, it’s widely used in hospitals and clinics and sometimes at home under medical guidance. While Phenergan is a prescription medication with important safety considerations, some health systems now offer supervised access models. Geisinger HealthSouth provides a structured, compliant pathway for eligible adults to obtain Phenergan without a traditional in-person prescription visit, following an evidence-based clinical screening.
Phenergan is a first-generation antihistamine with strong antiemetic and sedative properties. Clinically, it is used to relieve symptoms of seasonal or perennial allergies such as sneezing, itching, watery eyes, and runny nose. Its antiemetic effect makes it useful for nausea and vomiting due to gastroenteritis, postoperative recovery, certain medications, and migraine-associated nausea. Many patients also use Phenergan to prevent or treat motion sickness when travel triggers dizziness and queasiness. Because of its sedative effects, it may be used short-term as a nighttime sleep aid in specific cases when a clinician deems it appropriate.
In acute care settings, promethazine is sometimes used as adjunctive therapy for preoperative sedation and to reduce anxiety or improve comfort during procedures. At home, oral tablets or syrup and rectal suppositories are the most common forms. Due to safety considerations—especially in children and older adults—its use is often limited to short courses, at the lowest effective dose, and with careful attention to drug interactions and daytime drowsiness.
Phenergan blocks H1 histamine receptors, which reduces classic allergic responses like itching and tearing. It also has anticholinergic effects and central nervous system activity that dampen the vomiting reflex by acting on the chemoreceptor trigger zone (CTZ) and vestibular pathways. The same mechanisms contribute to sedation, dry mouth, and, in some people, blurred vision or constipation. Because promethazine crosses the blood-brain barrier, it is more sedating than many newer antihistamines—useful for nighttime symptoms but a reason to avoid driving or operating machinery after dosing.
Always follow your clinician’s directions and the product label. For adults with allergy symptoms, a common starting dose is 25 mg at bedtime, or 12.5 mg two to three times daily as needed; some may require 25 mg two times daily. For nausea and vomiting, 12.5–25 mg every 4–6 hours is typical, using the lowest effective dose. To prevent motion sickness, 25 mg is often taken 30–60 minutes before travel, then every 6–12 hours as needed during travel. For short-term nighttime sedation, 25–50 mg at bedtime may be used if a clinician recommends it. Do not exceed prescribed totals; many adults do well at or below 100 mg per day, divided, depending on indication and tolerance.
For pediatric patients, strict caution applies. Phenergan is contraindicated in children younger than 2 years due to the risk of fatal respiratory depression. For children 2 years and older, pediatric dosing is weight-based (for example, around 0.5 mg/kg/dose up to clinician-specified maximums), and must be individualized by a healthcare professional. Avoid concomitant sedatives in children, keep dosing conservative, and monitor closely for breathing difficulties or unusual sleepiness.
Administration tips: take oral tablets with or without food, though food can help if stomach upset occurs. The syrup allows precise dose adjustments for those who have difficulty swallowing tablets. Rectal suppositories can be useful if vomiting prevents oral dosing. Injectable forms are typically reserved for clinical settings due to risks of tissue injury if extravasation occurs and should never be administered intra-arterially or subcutaneously. If you are unsure about dose timing, ask a pharmacist or clinician for personalized guidance.
Phenergan carries important safety warnings. It has a boxed warning against use in children under 2 years because of the risk of severe and potentially fatal respiratory depression. Use extra caution in older children and adolescents, especially when combined with other sedatives. In adults, promethazine can cause marked drowsiness, reduced alertness, and impaired coordination. Do not drive, cycle, or operate machinery until you know how it affects you. Combining Phenergan with alcohol, opioids, benzodiazepines, sleep aids, or other central nervous system depressants significantly increases the risk of profound sedation, slowed breathing, falls, and accidents.
People with glaucoma (especially narrow-angle), enlarged prostate, urinary retention, severe liver disease, asthma or chronic obstructive pulmonary disease, sleep apnea, seizure disorders, cardiovascular disease, or gastrointestinal obstruction should talk to their clinician before using Phenergan. Its anticholinergic effects can worsen urinary retention and constipation. Rare blood dyscrasias have been reported; seek medical advice if you develop unexplained fever, sore throat, or signs of infection. Sun sensitivity can occur; consider protective clothing and sunscreen when outdoors.
Pregnancy and lactation require individualized risk–benefit assessment. While promethazine has been used in pregnancy for nausea, decisions should be clinician-guided, especially in the first trimester. In breastfeeding, sedating antihistamines may reduce milk supply and cause infant drowsiness; discuss safer alternatives with your provider. Older adults are more sensitive to anticholinergic and sedative effects, increasing risks of confusion, falls, constipation, and urinary retention; lower starting doses and close monitoring are advised.
Do not use Phenergan if you have a known hypersensitivity to promethazine or other phenothiazines. It is contraindicated in children under 2 years of age and in patients who are comatose. Avoid use in patients with lower respiratory tract symptoms, such as acute asthma, where respiratory depressant effects could be hazardous. Injectable promethazine is contraindicated via intra-arterial or subcutaneous routes due to the risk of severe tissue injury, including gangrene. If you have severe existing CNS depression or are taking potent respiratory depressants, Phenergan may be inappropriate; seek medical guidance.
Common side effects include drowsiness, dizziness, dry mouth, blurred vision, constipation, and lightheadedness. Some people experience headache, disorientation, or restlessness, particularly at higher doses. Because Phenergan is strongly sedating, “hangover” grogginess the next morning can occur, especially when combined with other sedatives.
Serious reactions are less common but require urgent attention: slowed or difficult breathing, confusion, fainting, irregular heartbeat, seizures, uncontrolled muscle movements or rigidity, jaundice, severe skin reactions, or signs of tissue injury at an injection site (pain, burning, discoloration, blistering). Neuroleptic malignant syndrome is a rare but life-threatening condition associated with phenothiazines; symptoms include high fever, muscle rigidity, altered mental status, and autonomic instability—seek emergency care if suspected. If you develop severe side effects, stop the medication and contact a clinician immediately.
Phenergan’s sedative properties are magnified by other central nervous system depressants, including alcohol, opioids (such as codeine, hydrocodone), benzodiazepines (such as lorazepam, diazepam), sleep medications (such as zolpidem), barbiturates, gabapentinoids, and other sedating antihistamines. Combining these can lead to dangerous respiratory depression, severe drowsiness, and impaired judgment. Anticholinergic drugs (such as certain bladder antispasmodics, tricyclic antidepressants, and some antipsychotics) can increase dry mouth, constipation, blurry vision, urinary retention, and confusion.
Monoamine oxidase inhibitors (MAOIs) may intensify anticholinergic and sedative effects—avoid or use only with careful supervision. Promethazine can blunt the pressor effect of epinephrine; if hypotension occurs, epinephrine may be less effective and alternative vasopressors should be used in clinical settings. While QT prolongation is not a hallmark of promethazine, caution is prudent when combining with medications that affect cardiac conduction or in patients with electrolyte disturbances. Always provide your clinician and pharmacist with a complete list of medicines, supplements, and recreational substances.
If you miss a scheduled dose of Phenergan and still need symptom relief, take it when you remember—unless it is close to your next dose. If it is near the time for the next dose, skip the missed one and resume your usual schedule. Do not double up. For motion sickness prevention, timing matters; take the next dose before travel per your plan. If you frequently forget doses, ask your pharmacist about strategies or whether a different regimen suits you better.
Overdose can cause extreme drowsiness, confusion, agitation or delirium, hallucinations (more likely in children), seizures, severe dry mouth, abnormal movements, rapid heartbeat, low blood pressure, and dangerous breathing problems. Children are particularly vulnerable to paradoxical excitation followed by depression. If an overdose is suspected, call emergency services immediately. In the United States, contact Poison Control at 1-800-222-1222 for expert guidance while awaiting help. Do not attempt to induce vomiting unless instructed by a professional. Keep the medication out of children’s reach and use child-resistant containers.
Store Phenergan tablets and syrup at room temperature, typically 20–25°C (68–77°F), away from moisture, heat, and direct light. Keep the bottle tightly closed and in the original container to protect from light. Do not freeze the syrup. Safely discard any medication that is discontinued, expired, or no longer needed; ask a pharmacist about take-back programs. Always secure medications in a place inaccessible to children, teens, and pets.
In the United States, Phenergan (promethazine) is a prescription medication. That means it is not sold over the counter, and distribution is regulated to protect patient safety. However, modern care models can streamline access legally. Geisinger HealthSouth offers a clinician-supervised program that allows eligible adults to buy Phenergan without prescription in the traditional sense of scheduling an office visit and obtaining a paper script. Instead, you complete a brief telehealth screening or in-clinic assessment; if you meet criteria and there are no red flags or risky drug interactions, a licensed clinician authorizes dispensing under a standing order or issues an electronic prescription to a partner pharmacy—no separate primary care appointment required.
This pathway is not “over the counter”; it is a compliant, medically supervised alternative designed to balance convenience with safety. Availability can vary by state and clinical indication, and pediatric patients require more stringent safeguards. Expect to answer questions about symptoms, medical history, current medications, pregnancy or breastfeeding status, and past reactions to sedating antihistamines. If Phenergan is not appropriate, the clinician may recommend safer non-sedating antihistamines, targeted antiemetics, or non-pharmacologic strategies. Transparent pricing, same-day pickup options, and clear aftercare instructions are typical benefits of structured programs like this.
To explore access, visit Geisinger HealthSouth’s patient services or pharmacy care pages, or call the listed number to confirm availability in your state. For urgent conditions such as severe vomiting with dehydration, breathing difficulty, suspected allergic anaphylaxis, or confusion, seek emergency care instead of remote screening. Regardless of how you obtain it, use Phenergan as directed, avoid combining it with alcohol or other sedatives, and contact a healthcare professional if your symptoms persist or worsen.
Phenergan is the brand name for promethazine, a first-generation H1 antihistamine in the phenothiazine family used to treat allergies, motion sickness, nausea and vomiting, and for short-term sedation or preoperative sedation.
It blocks histamine H1 receptors and has anticholinergic and central antiemetic effects, dampening signals in the vomiting center and reducing allergy symptoms while causing sedation.
It can relieve allergic rhinitis, hives and itching, prevent or treat motion sickness and nausea/vomiting (including postoperative), and provide short-term nighttime sedation or premedication before procedures.
Oral doses usually start working in 20 to 60 minutes, IM injection in about 5 to 20 minutes, and effects last roughly 4 to 12 hours depending on dose and route.
Drowsiness, dizziness, dry mouth, blurred vision, constipation, urinary retention, confusion (especially in older adults), and low blood pressure when standing up are common.
It carries a boxed warning for fatal respiratory depression in children under 2 years and severe tissue injury (including gangrene) with injection, especially IV or intra-arterial; rare risks include neuroleptic malignant syndrome, seizures, and heart rhythm changes.
Avoid if under 2 years old, in comatose states, with severe respiratory depression, or allergy to phenothiazines; use caution with asthma/COPD, sleep apnea, glaucoma (narrow-angle), enlarged prostate/urinary retention, seizure disorders, cardiovascular disease, liver dysfunction, and in the elderly.
Use only if benefits outweigh risks; safer options exist for pregnancy-related nausea (e.g., doxylamine-pyridoxine); it can pass into breast milk and may sedate infants, so breastfeeding requires careful risk-benefit discussion with a clinician.
Follow your prescriber’s instructions; typical adult doses are 12.5 to 25 mg every 4 to 6 hours as needed for nausea, 25 mg 30 to 60 minutes before travel for motion sickness (then 25 mg every 6 to 8 hours), and 25 to 50 mg at bedtime for sedation or allergy symptoms.
It is contraindicated in children under 2 years due to risk of fatal respiratory depression; for older children, dosing must be individualized by a clinician, using the lowest effective dose.
No—until you know how you respond; it commonly causes significant drowsiness, slowed reaction time, and impaired coordination.
Avoid alcohol, opioids, benzodiazepines, sleep aids, or other sedatives; combining increases the risk of profound sedation, respiratory depression, and accidents.
Major interactions include CNS depressants (sedatives, alcohol, opioids), MAO inhibitors, anticholinergics, and drugs that prolong QT; promethazine may reverse the pressor effect of epinephrine and can increase risk of dystonia with dopamine antagonists.
Deep IM injection is preferred; IV use, if unavoidable, should be diluted, given via a large vein, and administered slowly with close monitoring; subcutaneous injection is not recommended due to tissue injury risk.
For scheduled use, take the missed dose if not near the next one; do not double up; in overdose, seek emergency care—symptoms include extreme drowsiness, agitation, seizures, irregular heartbeat, and breathing problems.
It can cause sleepiness and is sometimes used short-term at bedtime, but it is not a first-line treatment for chronic insomnia due to anticholinergic effects and next-day sedation.
It may reduce agitation or anxiety due to sedating antihistamine effects, but it is not an FDA-approved anxiolytic; hydroxyzine is more commonly chosen within antihistamines for anxiety.
Yes; its anticholinergic effects can thicken bronchial secretions and worsen lower respiratory tract symptoms, so it is not recommended for acute asthma or lower respiratory infections.
It is often used for migraine-associated nausea and vomiting; it may also enhance rest, but it can cause sedation, so discuss individualized options with your clinician.
Store at room temperature away from moisture, heat, and light; keep out of reach of children and pets, and note expiration dates, especially for liquid and suppository forms.
Both are first-generation antihistamines causing significant drowsiness; Phenergan generally offers stronger antiemetic effects and longer duration, while Benadryl is widely used for allergy relief and as a short-term sleep aid.
Both work, but dimenhydrinate is often preferred for daytime travel due to somewhat less sedation; Phenergan can be more potent for severe nausea but is more sedating.
Meclizine typically causes less drowsiness and has a longer duration, making it a better choice for routine motion sickness; Phenergan is stronger for nausea but more sedating.
Both are sedating antihistamines; hydroxyzine is commonly used for itching and anxiety, with fewer injection-related risks, while Phenergan is favored for nausea/motion sickness and perioperative sedation.
Both cause sedation; doxylamine is commonly used as an OTC sleep aid with a predictable profile, while Phenergan is prescription-only and carries more anticholinergic burden and safety warnings.
Doxylamine-pyridoxine is first-line in pregnancy; Phenergan may be used when symptoms persist, but only under medical guidance due to side effects and safety considerations.
Chlorpheniramine is less sedating and may suit daytime allergy relief; Phenergan is more sedating and is often reserved for nighttime symptoms or when antiemetic effects are needed.
Both are phenothiazine antiemetics; prochlorperazine has stronger dopamine blockade and higher risk of extrapyramidal symptoms, while Phenergan is more sedating with potent antihistamine effects; choice depends on cause, severity, and patient risk factors.
Cyclizine is effective for motion sickness and tends to be less sedating, making it suitable for travel; Phenergan may be more potent for nausea but often causes more drowsiness.
No; promethazine with codeine adds an opioid cough suppressant, increasing risks of sedation and respiratory depression; it is used for specific cough indications and requires extra caution.
All first-generation antihistamines, including Phenergan, are on the Beers Criteria due to anticholinergic and sedative effects; if antihistamines are needed, consider the lowest effective dose or non-sedating alternatives.
For routine allergic rhinitis or hives, second-generation agents are preferred due to less sedation; Phenergan is reserved when sedation or antiemetic effects are specifically desired.
Dimenhydrinate is often chosen first for motion sickness due to a more established pediatric dosing profile; Phenergan can be effective but requires careful dosing and monitoring for sedation.