Skip to content

Phenylephrine

  • Prescription medicine
  • Prescription only
  • Identity checked
  • Sources last checked 2026-09-04

This page shows what was measured, who it was measured in, and what that does not settle.

What Phenylephrine does in the body

Increasing blood pressure

From the FDA-approved label: Phenylephrine is an alpha-1 adrenergic receptor agonist used for dilation of the pupil due to its vasoconstrictor and mydriatic action. Phenylephrine possesses predominantly α-adrenergic effects. In the eye, phenylephrine acts locally as a potent vasoconstrictor and mydriatic, by constricting ophthalmic blood vessels and the radial muscle of the iris.

What happened in people

RNAWiki has not yet published a reviewed conclusion for this use.

A fixed RNAWiki sentence

Where this came from

Wording RNAWiki always uses, not a finding about this substance.

No reviewed claim names a result for any goal on this record.

No source is stored against this line.

The limit that matters most

Not recorded.

Where it acts
Not recorded.
Kind of result
No result is published, so no kind of result applies yet
Supervision
RNAWiki has not recorded a supervision or regulatory status for this substance.

What the registries record it as

  • The substance registry classes this as chemical.

    FDA substance registry · 1WS297W6MV · read 2026-08-29

Where each sentence above came from

No recorded sentence describes the change this makes in a way that stands on its own. The page opens with what it is taken for instead, and the recorded explanation follows below.

Shown as the opening line on this page.

No statement of the main limit is recorded.

The four opening statements run to 69 words.

Words this page uses

Four words worth knowing first

Chosen from what this page shows, with each one explained before the word it depends on.

Stand-in result

A stand-in result is a number measured because the real result takes too long.

A picture of it, and where the picture fails

It is like judging a journey by the speedometer rather than by arriving.

Where that stops being true. Speed does predict arrival. Many stand-in results do not predict the real one.

What people get wrong. A stand-in result is often reported as the result itself.

A surrogate endpoint substituted for a clinical endpoint, valid only where the substitution has been shown to hold.

Enzyme

An enzyme is a protein that speeds up one chemical change.

A picture of it, and where the picture fails

An enzyme is like a machine on a production line doing one cut.

Where that stops being true. A machine is switched on and off by a person. Enzymes are controlled by the cell.

What people get wrong. Enzymes are thought to be used up. They are not; they work again and again.

A catalytic protein that lowers the activation energy of a specific reaction.

Receptor

A receptor is a part of a cell that a signal fits into.

A picture of it, and where the picture fails

A receptor is like a lock waiting for one key.

Where that stops being true. A lock either opens or does not. A receptor can be half-triggered, or worn out.

What people get wrong. Fitting a receptor is read as causing a benefit. It causes a step, and nothing more.

A protein that binds a specific ligand and converts that binding into a cellular response.

Pathway

A pathway is a chain of steps inside a cell, each one setting off the next.

A picture of it, and where the picture fails

A pathway is like a row of dominoes.

Where that stops being true. Dominoes fall one way. Pathways loop back and can switch themselves off.

What people get wrong. Changing one step is read as changing the outcome. Other steps often absorb it.

An ordered series of molecular interactions producing a defined cellular change.

What happened in peopleRead from sources, not yet reviewed

What was measured, goal by goal

One row for each goal a registered study measured something for. One column for each kind of thing that could be measured.

Registered studies list 40 outcome measures that RNAWiki could read. A registered study says what someone planned to measure. It does not say what they found. 0 of the matched studies tested this substance, and 0 posted a result.

There is no single score. A strong test result and a weak life result are different facts.

Goals down the side, kinds of measurement across the top. Each cell says what kind of thing was registered, not what was found.
GoalLife outcomeWhat a body can doHow a person feelsA test resultA step in the bodyHarmsHow longWho was studied
Healthy ageingWaiting for a reviewer1 registered study measure of this kind. No reviewed result yet.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Nothing in the sources checkedNo registered study lists a test result for this goal.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
FocusNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Nothing in the sources checkedNo registered study lists a test result for this goal.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Which registered measures put each goal on this table
Healthy ageing
hospital mortality
Focus
post operative cognitive dysfunction at 3 months

Sorted by fixed word lists, version v1. A name the rules do not recognise stays unsorted rather than moving to the nearest column.

What each mark on this table means
Waiting for a reviewer
1 registered study measure of this kind. No reviewed result yet.
Nothing in the sources checked
No registered study lists a performance measure for this goal.
Not recorded
Harms were not a registered measure for this goal.

What happened in peopleRead from sources, not yet reviewed

What happened in people

Each card is one study: the exact question it asked, who was in it, and whether it showed what it set out to show.

Postoperative Acute Kidney Injury

The study did not show it

Who was studied
NCT02726620
How many people
22435
Study design
Not applicable
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Acute Kidney Injury (AKI)

The study did not show it

Who was studied
NCT06802224
How many people
18000
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Number of Participants with a Composite of Major Perfusion-Related Complications

The study did not show it

Who was studied
NCT04884802
How many people
6254
Study design
Not applicable
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Number of Participants with a Composite of Major Perfusion-Related Complications

The study did not show it

Who was studied
NCT04934748
How many people
6254
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Number of Participants With Assigned Vasopressor Given

The study did not show it

Who was studied
NCT04789330
How many people
3626
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Proportion of participants with one or more intubation or anaesthesia related adverse events

The study did not show it

Who was studied
NCT06564857
How many people
2648
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Oral

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
What we know
RNAWiki holds 6 written-up human studies for this substance, each with the question it asked.
How we know it
Each card names the study, the number of people and what the study set out to measure.
What this does not prove
These summaries were written by a person and have not been signed off as reviewed claims.
Why it matters
A study that failed is as informative as one that worked, and both are here.
What we still do not know
No reviewed claim exists, so no exact population, effect size or interval is published yet.

What happened in peopleRead from sources, not yet reviewed

How close this is to real life

The top step is something a person would feel or care about. The bottom is a guess from software. Filled steps are where evidence exists for this substance.

  1. Living longer, or avoiding a major event Evidence recorded. Death, a heart attack, a stroke, a hospital stay.2 registered measures of this kind. No reviewed result.
  2. What a body can do day to day No evidence recorded. Walking, dressing, breathing, recovering.No registered study measures this.
  3. Measured performance No evidence recorded. How much was lifted, how far was run, how fast.No registered study measures this.
  4. Symptoms and quality of life No evidence recorded. Pain, tiredness, mood, sleep, as the person rated it.No registered study measures this.
  5. A number that stands in for health Evidence recorded. Cholesterol, blood sugar, bone density. A stand-in, not the thing itself.12 registered measures of this kind.
  6. A step measured inside a person Evidence recorded. Something measured in human tissue or human cells.1 registered measure inside human tissue.
  7. Animals Evidence recorded. Mice, rats, dogs. Useful for ideas, not proof about people.Stored records in Mouse, Rat. A result in animals says what to test next. It does not say what happens in people.
  8. Cells in a dish Evidence recorded. Cells or chemistry on a bench, far from a whole body.Stored mechanism abstracts describe steps measured in cells or tissue.
  9. A guess from software No evidence recorded. Nobody measured it. RNAWiki never publishes one as a finding.RNAWiki stores no prediction for this record. Software can suggest a link. RNAWiki does not publish one as a finding.

Higher on these steps means closer to something a person would feel. It does not mean better done.

What it would be like to takeRead from sources, not yet reviewed

Felt, measured, or meaningful

Three different things that get called the same word. Registered studies measured all three, and mixing them is how a blood test becomes a health claim.

Felt

Things a person could notice without a test.

No registered study measured anything of this kind.

Measured

Things only a test, a scale or a device shows.

  • blood pressure
  • time to reach plasma paracetamol concentration of 0 25
  • arterial blood pressure
  • maximum heart rate
  • systolic blood pressure
  • cerebral blood flow
  • heart rate after isoproterenol boluses
  • orthostatic change in heart rate
  • maternal blood pressure
  • bradycardia heart rate less than 50

and 3 more.

Meaningful

Things that change how a life goes, not only a number.

  • hospital mortality
  • stroke volume

A registered study says what someone planned to measure. It does not say what they found. A number moving is not the same as a life going better. The two are shown apart here.

Felt, but not shown to help. A person notices a change. No study showed it leads anywhere good.

Measured, but not felt. A number moves. The person notices nothing. Both can be true.

Measured, but not shown to matter. A number moves in the good direction. Nobody showed that lives went better.

Matters, but takes years. The result that counts may take longer than anyone would keep watching.

Names that fit none of the three (25)
  • systemic vascular resistance
  • choroidal blood flow
  • fundus pulsation amplitude
  • systemic and regional hemodynamics
  • pharmacokinetic parameters
  • optic nerve head pressure flow relationship
  • functional recruitment of capillaries in the skin
  • occurrence of postreperfusion syndrome
  • choroidal thickness
  • primary outcome
  • map while on vasopressors
  • hypotension
  • rescue boluses to maintain sbp
  • total rescue bolus dose of ephedrine to maintain sbp
  • best spectacle corrected visual acuity
  • post operative cognitive dysfunction at 3 months
  • muscle sympathetic nerve activity
  • incidence of hypotension
  • alpha 1 ab titer positive
  • icu stays greater than 1 5 days

These are harms, study-process measures, or names the rules did not recognise. They are shown rather than dropped.

What it would be like to takeRead from sources, not yet reviewed

How long anything takes

Nine different lengths of time that get confused with each other. None of them is worked out from another.

  1. Before anything is noticed. RNAWiki does not store this separately, and never works it out from another figure on this page.

  2. Before a test result moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  3. Before performance moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  4. How long the result was watched. No finished study window is recorded for a study that tested this substance.

  5. How long people took it. How long people actually took it is not stored. The study window is not the same thing.

  6. How long people were followed. Follow-up length is not stored separately. It is never read off the study window, which would be a different thing.

  7. How fast the body clears it. 2.5 hours hours

    Read from the label, which states: “The observed phenylephrine plasma terminal elimination half-life was 2.5 hours.”

  8. How long effects linger. RNAWiki does not store this separately, and never works it out from another figure on this page.

  9. Beyond the studies. Nothing is recorded about the long term.

    The longest finished study sets the edge of what anyone measured.

A study window is not how long people took it, and neither is how long they were followed. Where RNAWiki holds only one of the three, it shows one.

What is missing or unclearRead from sources, not yet reviewed

Were people like you studied?

RNAWiki cannot tell whether a study fits you. It can show who was in it, and where the result stops carrying.

Who was studied

People similar to this profile were included.

  • IMMPHENTIV injection 100 mcg/mL is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia. Phenylephrine Hydrochloride Injection 10 mg/mL is indicated for increasing blood pressure in adults with clinically important hypotension resulting primarily from vasodilation in the settings of anesthesia and septic shock.

Who is missing from the studies

  • Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What the label states about particular groups

  • On pediatric, the label states: “Safety and effectiveness in pediatric patients have not been established.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • On older people, the label states: “Clinical studies of phenylephrine did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Data from randomized controlled trials and meta-analyses with phenylephrine hydrochloride injection use in pregnant women during Cesarean section have not established a drug-associated risk of major birth defects and miscarriage.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • On people who are breastfeeding, the label states: “Risk Summary There are no data on the presence of phenylephrine hydrochloride injection or its metabolite in human or animal milk, the effects on the breastfed infant, or the effects on milk production.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • On people with reduced liver function, the label states: “In patients with liver cirrhosis [Child Pugh Class B and Class C], dose-response data indicate decreased responsiveness to phenylephrine.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • On people with reduced kidney function, the label states: “In patients with end stage renal disease (ESRD), dose-response data indicate increased responsiveness to phenylephrine.”

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

Where the result stopped carrying

  • This is a scope explorer, not a diagnosis engine.
  • It shows who was studied so you can see whether people similar to you were included.

RNAWiki cannot tell whether a study fits you. It can show who was in it.

What it would be like to takeRead from sources, not yet reviewed

Why it might seem to do nothing

A real effect and a noticed effect are different things. These are the recorded reasons the two come apart.

It was studied for a different goal

The studies measured something else entirely.

On this record: Some registered studies measured things that match no goal on this page.

It was studied in different people

The people in the studies were not much like the reader.

On this record: Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

The evidence may simply be wrong

Small early studies often do not hold up.

On this record: RNAWiki has not yet published a reviewed conclusion for this use.

Other reasons RNAWiki checked and found nothing for (10)
A different form was studied
The studied form is not the form on the shelf. Nothing in this record points to this reason.
There was nothing to correct
Where a level is already normal, topping it up may change nothing. Nothing in this record points to this reason.
Something else had to happen too
In the studies it was paired with training, a diet or another treatment. Nothing in this record points to this reason.
The change is too small to feel
A real change can still sit below what a person notices. Nothing in this record points to this reason.
Day-to-day swing hides it
Sleep, food, stress and time of day move most numbers more than this would. Nothing in this record points to this reason.
Not enough time yet
The studies ran longer than the person has waited. Nothing in this record points to this reason.
It was not taken as studied
Missed days change the result, and studies count them. Nothing in this record points to this reason.
Something else changed at the same time
Two changes at once cannot be told apart afterwards. Nothing in this record points to this reason.
The product may not be what it says
Contents of a sold product are not always what the label states. Nothing in this record points to this reason.
No recorded reason
RNAWiki has nothing stored that would explain it. Nothing in this record points to this reason.

None of these is a reason to take more. Taking more is not a step this page ever suggests.

What it would be like to takeRead from sources, not yet reviewed

What taking it involves

The recorded facts about getting hold of it and using it. Nothing here is a suggestion about what you should do.

How it is supplied

Prescription only

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

Read from the recorded approval status.

No source is stored against this line.

Form and route

Oral

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form and route recorded on this substance.

No source is stored against this line.

Who oversees it

RNAWiki has not recorded a supervision or regulatory status for this substance.

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

No register row and no identity class settled the question.

No source is stored against this line.

What is in the pack

Sold as syrup, tablet, solution, solution/drops, given by the oral, intravenous, ophthalmic route.

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

Recorded notes on how this is sold and what that means for what is in the pack.

No source is stored against this line.

Where it is registered

Regulatory records are listed in the technical disclosure at the foot of this page.

Counted from records

Where this came from

A count of rows RNAWiki holds. It describes our records, not your body.

Register entries are stored per jurisdiction and shown with their dates.

No source is stored against this line.

Why people stop

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

No record of why people stopped taking it is stored for this substance.

No source is stored against this line.

What it would be like to takeNothing found in the sources checked

What can go wrong

Sorted by where each line came from. A regulator's label and a report somebody sent in are not the same kind of fact.

Nothing found in the sources checked

No harm is recorded against this substance in the sources RNAWiki checked. Finding nothing is not the same as showing there is nothing.

The sources listed were searched and held nothing. That is not the same as nothing existing.

Reports sent to a regulator

  • These are reports people sent to a regulator. They do not show the medicine caused the reaction.
  • Nobody counted how many people took the medicine and reported nothing.
  • The same event can be reported more than once, and many reports are incomplete.
  • News coverage, lawsuits and new warnings change how often people report.
  • A count is not a rate and not a risk.

Phenylephrine appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 3249 reaction mentions were counted. One report can name several reactions.

The recorded terms (10)
  • drug hypersensitivity — 734 reaction mentions
  • pain — 454 reaction mentions
  • hypotension — 390 reaction mentions
  • toxicity to various agents — 333 reaction mentions
  • anaphylactic reaction — 255 reaction mentions
  • hypersensitivity — 254 reaction mentions
  • rheumatoid arthritis — 236 reaction mentions
  • bradycardia — 210 reaction mentions
  • hyperhidrosis — 196 reaction mentions
  • asthma — 187 reaction mentions
  • open-targets-adr · recorded 2026-06-24 · a recorded source, not a stored snapshot

Over a long time. No completed tested study window is recorded, so long-term effects are not established by the registry record.

Groups the studies covered thinly. Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What is missing or unclearRead from sources, not yet reviewed

Does the exact form matter?

Evidence belongs to the exact thing that was tested. A different salt, a different mixture or a different preparation is a different question.

The form that was studied

Oral

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form used in the studies cited on this page.

No source is stored against this line.

What is sold

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

Nothing further is recorded about which forms are sold.

No source is stored against this line.

What is recorded as being sold

  • 1726 products list this as an active ingredient in the United States drug directory. 227 of them contain it and nothing else.

    FDA National Drug Code directory · 71872-7273 · read 2026-08-29

  • They are sold as capsule, capsule, coated, capsule, gelatin coated, capsule, liquid filled, cloth and cream, taken intraocular, intravenous, nasal and ophthalmic.

    FDA National Drug Code directory · 71872-7273 · read 2026-08-29

  • The regulator's established pharmacologic class for it is adrenergic alpha1-agonists [moa] and alpha-1 adrenergic agonist [epc].

    FDA National Drug Code directory · 71872-7273 · read 2026-08-29

  • 1523 published labels name it as an active ingredient. 143 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · 88b68447-b016-4d5b-a5e3-c4ebccb14f8c · read 2026-08-29

  • Those labels are classed as human otc drug and human prescription drug.

    US prescribing information · 88b68447-b016-4d5b-a5e3-c4ebccb14f8c · read 2026-08-29

  • 400 marketed supplement labels list this ingredient, classed as other combinations.

    NIH Dietary Supplement Label Database · 267874 · read 2026-08-29

  • Those labels carry all other, nutrient and structure/function claims. A claim of that kind is written by the manufacturer and is not assessed by any regulator, so its presence says nothing about whether it is true.

    NIH Dietary Supplement Label Database · 267874 · read 2026-08-29

  • Phenylephrine Hydrochloride is intravenous at 3 DOSAGE FORMS AND STRENGTHS Phenylephrine hydrochloride Injection, 10 mg/mL, for intravenous use, is available in three vial sizes: Injection: 10 mg/mL as a clear, colorless solution in a single dose 1 mL vial (10 mg o…, recorded as fda label in effect 2021-11-16 in the United States.

    US prescribing information · abd39d9c-fcda-4d01-8a58-1d54ba7ac651 · read 2026-08-30

  • Recorded price in US: 5.13149–9.2005 USD per one millilitre, across 15 priced products whose strengths and pack forms differ, as of 2026-08-26, paid by retail pharmacies buying the product, as surveyed by the Centers for Medicare & Medicaid Services. It is not a list price, an insurance price, or what anyone pays at a counter..

    Recorded source · 2026-08-26 · read 2026-08-28

Evidence carries across two names for one substance. It does not carry across a salt, a mirror form or a mixture.

What it would be like to takeRead from sources, not yet reviewed

What you could measure

This one is decided with a clinician, so this section holds questions to ask rather than a plan to run.

RNAWiki could not confidently classify this substance, so no self-experiment plan is offered.

Questions worth asking

  • Which of the trials of Phenylephrine studied people like me?
  • What was measured, and for how long?
  • Was the result a laboratory value or a health outcome?
  • What would we watch for, and when would we stop?

Tracking can show whether something changed for you. It cannot show what caused it.

RNAWiki records evidence. It does not say whether this substance is right for you.

What is missing or unclearRead from sources, not yet reviewed

What nobody knows yet

Open questions, each with why it is open and what would close it.

Missing populations

Which groups were under-represented in the studies has not been recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing long-term data

No completed tested study window is recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

No reviewed conclusion

RNAWiki has not yet published a reviewed conclusion for this use.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing interaction studies

No interaction was found in the registers checked. Not finding one is not the same as showing there is none.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Formulation uncertainty

Several salts, forms or products of Phenylephrine are recorded. Results from one form may not transfer to another.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Mechanism not reviewed

No reviewed mechanism story exists for this substance.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

What happened in peopleRead from sources, not yet reviewed

Check any of this yourself

Every line above traced back to the study it came from. This is the technical layer, and the vocabulary changes here.

How many documents were read

  • 134 documents were read for this substance.

    RNAWiki source record

  • 30 of them state the same halfLife, and they agree.

    RNAWiki source record

  • 46 of them state the same volumeOfDistribution, and they agree.

    RNAWiki source record

Where else this substance is registered

FDA substance identifier (UNII)
1WS297W6MV
RxNorm concept
1049182

Checks this page had to pass

  • Passed

    Identity resolved

    no open identity hold

  • Passed

    No unresolved merge across substance families

    no quarantine open

  • Passed

    Every public sentence names a source

    The opening statement carries the origin: Written into the record, not signed off.

  • Not passed

    Trial roles classified for highlighted evidence

    No registered study is classified as testing this substance.

  • Passed

    No internal keys in reader text

    enforced by the copy-contract test over the rendered page

  • Not passed

    Safety mode resolved

    No register row and no identity class settled the question.

  • Passed

    Canonical metadata present

    slug and display name present

What is missing or unclearRead from sources, not yet reviewed

How this medicine reached us

Kept near the foot of the page. A historical event moves up only when it changes something about this substance today.

What the approval register records

  • 57 approved applications cover products containing this substance. The earliest was NDA008306, approved 19520121 to ANI PHARMS.

    Drugs@FDA application register · NDA008306 · read 2026-08-29

  • Marketing status on the register: discontinued, over-the-counter and prescription.

    Drugs@FDA application register · NDA008306 · read 2026-08-29

  • The earliest marketing start date recorded for a listed product is 19580630.

    FDA National Drug Code directory · 71872-7273 · read 2026-08-29

What is missing or unclearRead from sources, not yet reviewed

What to learn next

Ordered by what would most change how you read this page, starting with what is easiest to misunderstand.

This order is fixed in code and does not count clicks or time on the page.

What is not here

5 questions this page could not answer

These sections were prepared and left out because there was nothing to put in them. They are listed rather than hidden, so the gaps in this record are visible.

  • The path through the body — found nothing in the sources checked.
  • What it may clash with — found nothing in the sources checked.
  • Other ways to the same goal — found nothing in the sources checked.
  • Claims that go past the evidence — found nothing in the sources checked.
  • What changed on this page — found nothing in the sources checked.

The record as stored

The full record, for auditing

Everything above is built from what is below. This layer keeps the technical vocabulary, record identifiers and every stored row, so a reader who wants to check the page can.

Recorded evidence blocks (14)

What did Phenylephrine's largest trial (22435 people) and its longest (15 years) measure?


22435 people in Phenylephrine's largest registered study, 15 years in its longest registered window, measuring Hospital mortality. ClinicalTrials.gov · 2026-09-01

66 na, 46 phase4, 24 phase2, 23 phase3, 14 phase1, 9 early phase1, 6 na or unstated; NCT02673996; 2030-12-31. Last human test completed 2026, NCT07663149.

Interpretation These counts include studies where Phenylephrine was a comparison treatment, a background treatment or an exposure in an observational study, and the longest window may be a planned end date. Trial roles have not yet been classified for this record.

Show the evidence
  • na
    66
  • phase4
    46
  • phase2
    24
  • phase3
    23
  • phase1
    14
  • early phase1
    9
2 more recorded rows
  • na or unstated
    6
  • Last recorded human test NCT07663149
    2026-06-07

recorded 2026-09-01 · last checked 2026-09-04

From mouse to human: where has Phenylephrine shown lifespan?


mouse: mechanism-only, rat: mechanism-only and human: lifespan (178): the rungs where Phenylephrine has a recorded finding. Europe PMC and ClinicalTrials.gov · organism ladder · 2026-09-01

Interpretation Hospital mortality — the recorded outcome words.

Yeast C. elegans Drosophila Mouse mechanism-onlyRat mechanism-onlyDog Non-human primate Human lifespan
Show the evidence
  • mouse
    mechanism-only
  • rat
    mechanism-only
  • human NCT02118467
    lifespan; Hospital mortality; 178

recorded 2026-09-01 · last checked 2026-09-04

19 of Phenylephrine's trials stopped: safety, accrual/recruitment, funding/business, sponsor decision unspecified, other?


safety (2), accrual/recruitment (9), funding/business (1), sponsor decision unspecified (1) and other (6): Phenylephrine's stop wording, clustered. ClinicalTrials.gov · 2026-09-01

"Study is no longer required by Brazil health authority."; 19 of 178 registered studies

Show the evidence

Trial

  • NCT01026961
    withdrawn; "Study is no longer required by Brazil health authority."
  • NCT01048125
    terminated; "Due to difficulty in recruitment and resource restraints"
  • NCT01092975
    terminated; "formulation/dose changes; planned changes to safety monitoring/reporting"
  • NCT01243970
    terminated; "Change in clinical practice since the start of the trial in 2011 (phenylephrine superior)"
  • NCT02025426
    terminated; "Significant challenges recruiting a difficult patient population with most surgeries occurring out of hours"
  • NCT02101047
    withdrawn; "lack of eligible participant"
13 further recorded trials
  • NCT02203630
    terminated; "Slow enrollment; Lack of support and equipoise"
  • NCT02245230
    terminated; "We were not able to enroll adequate number of participants that met the inclusion/exclusion criteria, and we run out of funding."
  • NCT02428062
    suspended; "Pending Pilot study results evaluation"
  • NCT03098680
    terminated; "Unable to recruit in time before end of PhD studentship"
  • NCT03972683
    withdrawn; "no participants enrolled"
  • NCT04218773
    suspended; "seeking additional funding"
  • NCT04610801
    withdrawn; "Study Period Ended/ Not Completed"
  • NCT04777383
    terminated; "The study was terminated prematurely due to insufficient operational resources to continue trial conduct and completion. The decision was unrelated to safety concerns or study outcomes."
  • NCT04839224
    terminated; "Slow Patient Enrollment"
  • NCT05070650
    withdrawn; "Sandoz has decided to withdraw the clinical study due to internal business reasons. No patients were enrolled in any of the participating countries."
  • NCT05109611
    terminated; "Recruitment challenges, i.e., not able to meet sample size targeted; secondary to the changing landscape of COVID-19 infection pathology."
  • NCT05290987
    terminated; "Number of participants needed not reached (13/80)"
  • NCT05883449
    terminated; "Due to sponsor decision"

recorded 2026-09-01 · last checked 2026-09-04

Human studies of Phenylephrine used Phenylephrine 100 mcg — over how long?


Human studies of Phenylephrine used "Phenylephrine 100 mcg". ClinicalTrials.gov · 2026-09-01

10 recorded entries; human; intravenous; also "Phenylephrine Unimedic 10mg/ml", "Phenylephrine, 10 mg/ml, Unimedic", "Phenylephrine Hydrochloride 4 mg"

Show the evidence

human

  • NCT03702400
    Phenylephrine 100 mcg
  • NCT03858465
    Phenylephrine Unimedic 10mg/ml
  • NCT04777383
    Phenylephrine, 10 mg/ml, Unimedic
  • NCT05348980
    Phenylephrine Hydrochloride 4 mg
  • NCT05348980
    Phenylephrine Hydrochloride 8 mg
  • NCT05639959
    Mometasone Nasal 50 Mcg/Inh Nasal Spray
4 more recorded rows
  • human NCT05706727
    intravenous; intravenous bolus dose of phenylephrine 50 mcg
  • human NCT06648850
    DA-010 - Oral Phenylephrine 20 mg + DA-005 Oral (HIF-1α supplement)
  • human NCT06648850
    Phenylephrine Topical 0.25% + Intact Pro Topical
  • human NCT07153601
    Phenylephrine 50 mcg

recorded 2026-09-01 · last checked 2026-09-04

Phenylephrine's half-life is 2.5 hours — which schedules were studied?


2.5 hours, the half-life Phenylephrine's label states. openfda-label · e1a7ab4b-0afe-4463-a039-5be0323cf2f7 · 2026-08-30

Show the evidence
  • half life
    2.5 hours hours; The observed phenylephrine plasma terminal elimination half-life was 2.5 hours.
  • metabolism
    A mass balance study showed that phenylephrine is extensively metabolized by the liver with only 12% of the dose excreted unchanged in the urine.

recorded 2026-08-30 · last checked 2026-09-04

Could one person measure Phenylephrine's effect on blood pressure?


Blood pressure: measured in Phenylephrine's trials.

Interpretation blood pressure is the recorded endpoint.

Show the evidence

biomarkers

  • blood pressure; 2026-09-01
  • systemic vascular resistance; 2026-09-01
  • choroidal blood flow; 2026-09-01
  • fundus pulsation amplitude; 2026-09-01
  • systemic and regional hemodynamics; 2026-09-01
  • pharmacokinetic parameters; 2026-09-01
14 more recorded rows
  • biomarkers
    optic nerve head pressure flow relationship; 2026-09-01
  • biomarkers
    functional recruitment of capillaries in the skin; 2026-09-01
  • biomarkers
    occurrence of postreperfusion syndrome; 2026-09-01
  • biomarkers
    time to reach plasma paracetamol concentration of 0 25; 2026-09-01
  • biomarkers
    choroidal thickness; 2026-09-01
  • biomarkers
    primary outcome; 2026-09-01
  • biomarkers
    arterial blood pressure; 2026-09-01
  • biomarkers
    map while on vasopressors; 2026-09-01
  • biomarkers
    hospital mortality; 2026-09-01
  • biomarkers
    maximum heart rate; 2026-09-01
  • biomarkers
    systolic blood pressure; 2026-09-01
  • biomarkers
    cerebral blood flow; 2026-09-01
  • biomarkers
    hypotension; 2026-09-01
  • biomarkers
    rescue boluses to maintain sbp; 2026-09-01
  • half life
    2026-09-04; halfLife; hours; 2.5 hours; 2026-08-30
  • human trials at or under30
    42
  • smallest human trial
    0; NCT01026961; PHASE1/PHASE2; the smallest recorded human enrolment at or below 30; the registry states no direction of its result; WITHDRAWN

Which of alpha 1 ab titer positive, arterial blood pressure and autoantibody levels did Phenylephrine's trials measure?


alpha 1 ab titer positive, arterial blood pressure and autoantibody levels lead 40 outcome terms across Phenylephrine's trials. ClinicalTrials.gov · 2026-09-01

Interpretation fundus pulsation amplitude, systemic and regional hemodynamics, pharmacokinetic parameters, optic nerve head pressure flow relationship, functional recruitment of capillaries in the skin and occurrence of postreperfusion syndrome follow.

Show the evidence
  • blood pressure
    1
  • systemic vascular resistance
    1
  • choroidal blood flow
    1
  • fundus pulsation amplitude
    1
  • systemic and regional hemodynamics
    1
  • pharmacokinetic parameters
    1
14 more recorded rows
  • optic nerve head pressure flow relationship
    1
  • functional recruitment of capillaries in the skin
    1
  • occurrence of postreperfusion syndrome
    1
  • time to reach plasma paracetamol concentration of 0 25
    1
  • choroidal thickness
    1
  • primary outcome
    1
  • arterial blood pressure
    1
  • map while on vasopressors
    1
  • hospital mortality
    1
  • maximum heart rate
    1
  • systolic blood pressure
    1
  • cerebral blood flow
    1
  • hypotension
    1
  • rescue boluses to maintain sbp
    1

recorded 2026-09-01 · last checked 2026-09-04

Which of Phenylephrine's 21 ongoing trials reports first?


21 registered trials of Phenylephrine are open; earliest completion 2025-11-28. ClinicalTrials.gov · 2026-09-01

Mean arterial blood pressure (MAP); Hospital mortality; latest 2030-12-31

Show the evidence

Trial

  • NCT01731444
    "Phenylephrine Tumescence for Hemostasis in Surgery for Burn Injury"; n 24; "Mean arterial blood pressure (MAP)"; 2028-12-31
  • NCT02118467
    "Vasoactive Drugs in Intensive Care Unit"; n 836; "Hospital mortality"; 2026-12-01
  • NCT02560805
    "Role of Sympathetic Overactivity and Angiotensin II in PTSD and CV"; n 134; "Change in Muscle Sympathetic Nerve Activity (MSNA)"; 2027-03-30
  • NCT02673996
    "POTS Adrenergic Ab (CIHR Aims #1&2)"; n 125; "The proportion of alpha-1 Ab titer positive subjects"; 2030-12-31
  • NCT02725060
    "Autoimmune Basis for Postural Tachycardia Syndrome"; n 58; "Autoantibody levels"; 2026-12
  • NCT03620942
    "Development of Advanced Double Intravenous Vasopressor Automated (ADIVA) System"; n 173; "Number of events of Hypotension occurrence"; 2027-12-31
14 further recorded trials
  • NCT04053478
    "Effects of Ephedrine, Phenylephrine, Norepinephrine and Vasopressin on Contractility of Human Myometrium and Umbilical Vessels: An In-vitro Study"; n 144; "Motility index"; 2026-12
  • NCT04500899
    "Use of Phenylephrine for Assessment of Mitral Regurgitation Severity"; n 35; "The percentage of patients with greater than 25% increase in MR regurgitant volume (Rvol) after the use of phenylephrine during transesophageal echocardiography."; 2026-06
  • NCT04934748
    "The GUARDIAN Trial - Vasopressor Sub-Study"; n 6254; "Number of Participants with a Composite of Major Perfusion-Related Complications"; 2027-04-25
  • NCT05997732
    "Sympathetic Neurovascular Transduction: Role of Adrenergic Receptors and Sex Differences"; n 30; "Forearm blood flow"; 2027-12-01
  • NCT06083948
    "Vasopressor Impact on Brain Circulation, Organ Blood Flow and Tissue Oxygenation During Anesthesia"; n 32; "Cerebral blood flow"; 2027-12-31
  • NCT06265220
    "AB-101 in Combination With B-Cell Depleting mAb in Patients Who Failed Treatment for Class III or IV Lupus Nephritis or Other Forms of Refractory Systemic Lupus Erythematosus"; n 51; "Incidence of Treatment-Emergent Adverse Events and Serious Adverse Events"; 2027-08
  • NCT06285396
    "Effect of Ephedrine, Phenylepinephrine, and Norepinephrine on Myometrial Contractility in Pregnant People With Type II and Gestational Diabetes During Cesarean Section: An In-vitro Study"; n 96; "Motility index"; 2026-12
  • NCT06581562
    "Open-label Single-Center Study to Evaluate the Safety and Efficacy of Combining Rituximab and AB-101 in B-cell Associated Autoimmune Diseases."; n 30; "Incidence of adverse events and relationship to study drug"; 2028-12
  • NCT06648850
    "Clinical Study of DA-001 as a Treatment for Hair Shedding Reduction and Hair Re-Growth"; n 1120; "Mean Change in Hair Shedding"; 2027-04-26
  • NCT06770426
    "CompARing Between CO2 Phenylephrine and Phenylephrine Only Treatment in Patients With proGrEssing Cerebral infarctioN"; n 40; "percent improvement of NIHSS score in each group"; 2027-12
  • NCT06802224
    "The Choice of Vasopressor to Prevent Postoperative Acute Kidney Injury After Major Non-Cardiac Surgery"; n 18000; "Acute Kidney Injury (AKI)"; 2028-07
  • NCT06855745
    "Phase 2 Randomized Double-blind Study to Assess Topical Zabalafin Hydrogel Vs Vehicle in Mild to Moderate AD."; n 72; "To evaluate the efficacy of zabalafin hydrogel compared with vehicle in treating mild to moderate AD as assessed by vIGA."; 2025-11-28
  • NCT07033845
    "Pharmacokinetic Study of Topical Phenylephrine"; n 24; "Pharmacokinetic profile of phenylephrine"; 2025-12-28
  • NCT07386873
    "The Efficacy of Olfactory Cleft Steroid Drops in Patients With CRS With Olfactory Cleft Obstruction"; n 54; "The Sniffin' Sticks test"; 2028-12-31

recorded 2026-09-01 · last checked 2026-09-04

Which running trial of Phenylephrine could settle lifespan?


NCT02118467 measures Hospital mortality, reading out 2026-12-01.

1 open trial; n 836; "Vasoactive Drugs in Intensive Care Unit"

Show the evidence
  • Trial NCT02118467
    "Vasoactive Drugs in Intensive Care Unit"; n 836; "Hospital mortality"; 2026-12-01

Which 72 trials of Phenylephrine posted no result?


Posted no result
72 of 72 completed trials
Registrations
NCT00373802, NCT00379691, NCT00481442, NCT00199784, NCT00639015 and NCT00585091, and 66 more
Completion dates
oldest 2005-06; newest 2024-08-20
Show the evidence

Trial

  • NCT00373802
    2005-06
  • NCT00379691
    2006-12
  • NCT00481442
    2007-03
  • NCT00199784
    2007-04
  • NCT00639015
    2008-06
  • NCT00585091
    2008-08
14 further recorded trials
  • NCT00762567
    2008-11
  • NCT02885168
    2009-04
  • NCT01024543
    2009-11
  • NCT01006863
    2010-03
  • NCT00996190
    2010-08
  • NCT04534452
    2012-06-06
  • NCT04025918
    2012-07
  • NCT01509521
    2012-08
  • NCT00806741
    2012-09
  • NCT01278238
    2012-10
  • NCT01609491
    2012-12
  • NCT02802683
    2016-06
  • NCT02585570
    2016-09
  • NCT02739399
    2016-09

At the median, Phenylephrine's trials enrolled 71 people — anything larger?


Median enrolment
71
Largest enrolment
22435
Registered trials counted
178

What do 3249 spontaneous reports say about Phenylephrine — and not say?


These are reports people sent to a regulator. They do not show the medicine caused the reaction. Nobody counted how many people took the medicine and reported nothing. The same event can be reported more than once, and many reports are incomplete. News coverage, lawsuits and new warnings change how often people report. A count is not a rate and not a risk.

Phenylephrine appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 3249 reaction mentions were counted: drug hypersensitivity 734; pain 454; hypotension 390; toxicity to various agents 333. open-targets-adr · CHEMBL1200339 · 2026-06-24

Show the evidence
  • drug hypersensitivity
    734
  • pain
    454
  • hypotension
    390
  • toxicity to various agents
    333
  • anaphylactic reaction
    255
  • hypersensitivity
    254
4 more recorded rows
  • rheumatoid arthritis
    236
  • bradycardia
    210
  • hyperhidrosis
    196
  • asthma
    187

recorded 2026-06-24 · last checked 2026-09-04

Was Phenylephrine studied with fasting and exercise?


fasting and exercise are named in Phenylephrine's label sentences: "This single-center, randomized, open-label bioequivalence program compared two fixed-dose combination (FDC) tablets containing ibuprofen (200 mg) and phenylephrine hydrochloride (10 mg) from different manufacturers in healthy Chinese adults under fasting and fed conditions." openfda-label+europepmc · 2025-11-14

2 recorded statements; fasting, exercise

Show the evidence
  • fasting
    This single-center, randomized, open-label bioequivalence program compared two fixed-dose combination (FDC) tablets containing ibuprofen (200 mg) and phenylephrine hydrochloride (10 mg) from different manufacturers in healthy Chinese adults under fasting and fed conditions.
  • exercise
    Isometric exercise increased choroidal blood flow during administration of placebo and phenylephrine, but not during administration of L-NMMA (P < 0.001 vs. placebo).

recorded 2025-11-14 · last checked 2026-09-04

What is recorded about Phenylephrine and AMPK?


"This reliance on TFEB for growth trigger-induced AMPK signaling was also observed in vitro in cells exposed to phenylephrine, as were the antihypertrophic effects of TFEB activation, supporting a direct role of TFEB in this process." — where Phenylephrine and AMPK appear together. Europe PMC · pathway abstract search · 2026-06-16

AMPK, sirtuin, NAD+, autophagy; PMID 42299666, 42223184, 40865637, 36914083

Show the evidence
  • AMPK PMID 42299666
    "This reliance on TFEB for growth trigger-induced AMPK signaling was also observed in vitro in cells exposed to phenylephrine, as were the antihypertrophic effects of TFEB activation, supporting a direct role of TFEB in this process."
  • sirtuin PMID 42223184
    "However, SIRT2 inhibition did attenuate the phenylephrine-mediated hypertrophic response in H9c2 cells."

AMPK

  • PMID 40865637
    "Moreover, the acetylation-mimetic mutant mitigated phenylephrine-induced mitochondrial dysfunction and cardiomyocyte hypertrophy via AMPK activation."
  • PMID 36914083
    "In addition, incubation with AMPK activators reduced the phenylephrine-induced contraction of endothelium-denuded HPA from Non-PH and PH patients."
  • sirtuin PMID 21414296
    "SIRT1 upregulation by phenylephrine was not associated to changes in NAD(+) levels, but was blocked by inhibitors of AMP-activated Protein Kinase (AMPK) or by AMPK knockdown by siRNA."
  • NAD+ PMID 21414296
    "SIRT1 upregulation by phenylephrine was not associated to changes in NAD(+) levels, but was blocked by inhibitors of AMP-activated Protein Kinase (AMPK) or by AMPK knockdown by siRNA."
  • sirtuin PMID 21414296
    "When SIRT1 was inhibited with sirtinol or downregulated by siRNA, H9c2 cell viability was significantly decreased following phenylephrine treatment, showing that SIRT1 improves cell survival under hypertrophic stress."

autophagy

  • PMID 37272106
    "Myocardial cells were classified from TAC mice into five groups: Control, Trehalose, Phenylephrine (PE), PE+Trehalose, and PE+Trehalose+autophagy inhibitor chloroquine groups."
  • PMID 33321735
    "These results indicate that phenylephrine inhibits hepatic steatosis through stimulation of β-oxidation and autophagy in the liver."

recorded 2026-06-16 · last checked 2026-09-04

Where it is registered
Identifiers, relations and other names

The exact record

ChEMBL id
CHEMBL1200339
PubChem CID
16745125
CAS number
939-38-8
RxCUI
8163
InChIKey
SONNWYBIRXJNDC-VIFPVBQESA-N
Also called
PHENYLEPHRINE HYDROCHLORIDE, Cyclomydril, Duo-medihaler, Fenilefrina, Meta-synephrine, Metasynephrine, M-oxedrine, M-sympathol, M-sympatol, M-synephrine, Phenylephrine minims, R(-)-mezaton
Salt form
Afrin 4 hour nasal spray, Phenylephrine hydrochloride component of advil congestion relief, Phenylephrine hydrochloride component of cyclomydril, Phenylephrine hydrochloride component of mydcombi, Phenylephrine hydrochloride component of omidria, Phenylephrine hydrochloride component of phenergan vc, Phenylephrine hydrochloride component of pherazine vc, Phenylephrine hydrochloride component of prefrin-a, Phenylephrine hydrochloride component of promethazine vc, phenylephrine hcl, Phenylephrine acid tartrate, Phenylephrine bitartrate component of duo-medihaler
Trade name
Biorphen, Fenilfar, Fenox, Immphentiv, Mydfrin, Nazex, Neosynephrine, Neo-synephrine, Nostril, Nurofen sinus pain relief, Prefrin, Vazculep
Development code
NSC-757273, AB-101 (PHENYLEPHRINE), J8.601K, AB101
Sources (11)

Sources

  • ClinicalTrials.gov clinicaltrials.gov ·
  • ClinicalTrials.gov ClinicalTrials.gov API v2 snapshot 2026-09-01T09:00:05 ·
  • this record's own fields 2,3,5 ·
  • Europe PMC dose-response search ·
  • Europe PMC pathway abstract search ·
  • Europe PMC search ·
5 more sources

ClinicalTrials.gov — US Government work · Europe PMC — metadata only, under the recorded legal gate · Open Targets 26.06 — CC0 · derived from this page's own recorded fields; no external licence · mixed register set; per-register licences in docs/specs/corpus-20k-sources.md · openFDA / DailyMed — US Government work

How these records are assembled · Which registers were checked

Index-quality checks
  • identity passed: no open identity hold
  • required summary fields resolved: 5 required field(s) not terminal: Why people use it, Best-supported result, Most important common problem, Biggest unanswered question, Human evidence
  • public claims reviewed: 0 reviewed claim(s); drafts are never rendered
  • source coverage passed: 11 source rows
  • no critical contamination: no quarantine open
  • canonical metadata passed: slug and display name present
  • no raw internal fields: enforced by the copy-contract test over the rendered page

This is a record of evidence. It is not medical advice, and it does not say this substance suits you. Nothing here says any substance on RNAWiki is appropriate for a child.