Propranolol label

Propranolol

Propranolol Recall

Get an alert when a recall is issued.

Add Info

Side Effects & Adverse Reactions

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

•
more than 4,000 mg of acetaminophen in 24 hours
•
with other drugs containing acetaminophen
•
3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

•
skin reddening
•
blisters
•
rash

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: If sore throat is severe, lasts for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

•
with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
•
if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
•
if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

•
liver disease
•
heart disease
•
high blood pressure
•
thyroid disease
•
diabetes
•
trouble urinating due to an enlarged prostate gland
•
cough that occurs with too much phlegm (mucus)
•
persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

When using this product

do not use more than directed

Stop use and ask a doctor if

•
you get nervous, dizzy or sleepless
•
pain, nasal congestion or cough gets worse or lasts more than 7 days
•
fever gets worse or lasts more than 3 days
•
redness or swelling is present
•
new symptoms occur
•
cough comes back or occurs with rash or headache that lasts.

These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Do not use

•
with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
•
if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
•
if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

•
liver disease
•
heart disease
•
high blood pressure
•
thyroid disease
•
diabetes
•
trouble urinating due to an enlarged prostate gland
•
cough that occurs with too much phlegm (mucus)
•
persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

Stop use and ask a doctor if

•
you get nervous, dizzy or sleepless
•
pain, nasal congestion or cough gets worse or lasts more than 7 days
•
fever gets worse or lasts more than 3 days
•
redness or swelling is present
•
new symptoms occur
•
cough comes back or occurs with rash or headache that lasts.

These could be signs of a serious condition.

Add Info

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Add Info

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

Add Info

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Add Info

Uses

temporarily relieves common cold/flu symptoms:

•
nasal congestion
•
cough due to minor throat and bronchial irritation
•
sore throat
•
headache
•
minor aches and pains
•
fever
Add Info

History

There is currently no drug history available for this drug.

Add Info

Other Information

There are no additional details available for this product.

Add Info
Add to My Alerts
Report Side Effect
Leave a Review

Is this a good medication?

Rated 5 out of 5
5.00
out of Five Stars
1
Rating(s)
Navigate to :
Propranolol Recall
Side Effects & Adverse Reactions
Legal Issues
FDA Safety Alerts
Manufacturer Warnings
FDA Labeling Changes
Uses
History
Other Information
Manufacturers
Trending Topics

Propranolol Manufacturers

  • West-ward Pharmaceutical Corp
    Propranolol | Publix Super Markets Inc
    No Recall

    Propranolol | Publix Super Markets Inc

    Propranolol | Publix Super Markets Inc
    • take only as directed – see overdose warning • do not exceed 4 doses per 24 hrs

    adults & children 12 yrs & over

    2 softgels with water every 4 hrs

    children 4 to under 12 yrs

    ask a doctor

    children under 4 yrs

    do not use

    Other information • store at 20-25 °C (68-77 °F)
  • Stat Rx Usa Llc
    Propranolol |
    No Recall

    Propranolol |

    Propranolol |
  • Physicians Total Care, Inc.
    Propranolol | Physicians Total Care, Inc.
    No Recall

    Propranolol | Physicians Total Care, Inc.

    Propranolol | Physicians Total Care, Inc.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    The usual dose is 1 to 3 mg administered under careful monitoring, such as electrocardiography and central venous pressure. The rate of administration should not exceed 1 mg (1 mL) per minute to diminish the possibility of lowering blood pressure and causing cardiac standstill. Sufficient time should be allowed for the drug to reach the site of action even when a slow circulation is present. If necessary, a second dose may be given after two minutes. Thereafter, additional drug should not be given in less than four hours. Additional propranolol hydrochloride should not be given when the desired alteration in rate or rhythm is achieved.

    Transfer to oral therapy as soon as possible.

  • General Injectables & Vaccines, Inc
    Propranolol | General Injectables & Vaccines, Inc
    No Recall

    Propranolol | General Injectables & Vaccines, Inc

    Propranolol | General Injectables & Vaccines, Inc

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    The usual dose is 1 to 3 mg administered under careful monitoring, such as electrocardiography and central venous pressure. The rate of administration should not exceed 1 mg (1 mL) per minute to diminish the possibility of lowering blood pressure and causing cardiac standstill. Sufficient time should be allowed for the drug to reach the site of action even when a slow circulation is present. If necessary, a second dose may be given after two minutes. Thereafter, additional drug should not be given in less than four hours. Additional propranolol hydrochloride should not be given when the desired alteration in rate or rhythm is achieved.

    Transfer to oral therapy as soon as possible.

  • App Pharmaceuticals, Llc
    Propranolol | App Pharmaceuticals, Llc
    No Recall

    Propranolol | App Pharmaceuticals, Llc

    Propranolol | App Pharmaceuticals, Llc

    The usual dose is 1 mg to 3 mg administered under careful monitoring, such as electrocardiographiy and central venous pressure.  The rate of administration should not exceed 1 mg (1 mL) per minute to diminish the possibility of lowering blood pressure and causing cardiac standstill.

    Sufficient time should be allowed for the drug to reach the site of action even when a slow circulation is present.  If necessary, a second dose may be given after two minutes.  Thereafter, additional drug should not be given in less than four hours.  Additional propranolol hydrochloride should not be given when the desired alteration in rate and/or rhythm is achieved.

    Transfer to oral therapy as soon as possible.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Login To Your Free Account