Lortuss Lq
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Questions & Answers
Side Effects & Adverse Reactions
Do not exceed recommended dosage.
- 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.
- a breathing problem such as emphysema or chronic bronchitis especially in children
- glaucoma
- trouble urinating due to an enlarged prostate gland
- heart disease
- high blood pressure
- thyroid disease
- diabetes mellitus
now taking sedatives or tranquilizers.
- may cause excitability especially in children
- may cause marked drowsiness
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase the drowsiness effect
- be careful when driving a motor vehicle or operating machinery
- nervousness, dizziness, or sleeplessness occur
- symptoms do not improve within 7 days or are accompanies by fever
- new symptom occur
ask a health professional before use.
In case of accidental overdose seek professional help or contact a Poison Control Center immediately.
- 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.
- a breathing problem such as emphysema or chronic bronchitis especially in children
- glaucoma
- trouble urinating due to an enlarged prostate gland
- heart disease
- high blood pressure
- thyroid disease
- diabetes mellitus
now taking sedatives or tranquilizers.
Stop use and ask a doctor if- nervousness, dizziness, or sleeplessness occur
- symptoms do not improve within 7 days or are accompanies by fever
- new symptom occur
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- runny nose
- itching of the nose or throat
- itchy, watery eyes
- nasal congestion
- reduces swelling of nasal passage
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Lortuss Lq Manufacturers
-
Sallus Laboratories, Llc
![Lortuss Lq (Doxylamine Succinate, Pseudoephedrine Hydrochloride) Liquid [Sallus Laboratories, Llc]](/wp-content/themes/bootstrap/assets/img/loading2.gif)
Lortuss Lq | Sallus Laboratories, Llc
Do not exceed recommended dosage. Adults and children
12 years of age and older:
2 teaspoonfuls (10 mL) every
6 hours, not to exceed
8 teaspoonfuls in 24-hour
period or as directed by a doctor.
Children 6 to under
12 years of age:
1 teaspoonful (5 mL) every
6 hours, not to exceed
4 teaspoonfuls in a 24-hour
period or as directed by a doctor.
Children under 6 years of age:
Consult a doctor
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