Overview
Pheniramine is a first-generation antihistamine in the alkylamine class, similar to brompheniramine and chlorpheniramine. It is used in some over-the-counter allergy as well as cold & flu products in combination with other drugs. Pheniramine's use as an anti-allergy medication has largely been supplanted by second-generation antihistamines such as cetirizine and loratadine.
Indication
常用于过敏性疾病和感冒等。
Associated Conditions
- Allergic Conjunctivitis (AC)
- Allergic Skin Reaction
- Allergic urticaria
- Anaphylaxis
- Angioedema
- Atopic Dermatitis
- Burns first degree
- Common Cold
- Congestion of the Conjunctivas
- Drug hypersensitivity reaction
- Flu caused by Influenza
- Insect Bites
- Neurodermatitis
- Ocular Irritation
- Red eye
- Sunburn
- Urticaria
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| NAPHCON-A STERILE OPHTHALMIC SOLUTION | SIN04717P | SOLUTION | 3.0 mg/ml | 6/13/1990 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| REDISIL EYE DROPS | N/A | N/A | N/A | 1/27/2022 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| VISINE ALLERGY eye drops bottle | 66073 | Medicine | A | 9/17/1998 | |
| NAPHCON-A eye drops bottle | 47652 | Medicine | A | 1/24/1994 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| PULMORPHAN | laboratoire riva inc. | 00513741 | Syrup - Oral | 7.5 MG / 5 ML | 12/31/1978 |
| ODAN-VERNACON | odan laboratories ltd | 00626643 | Solution - Ophthalmic | 0.5 % | 12/31/1986 |
| COLD STIX | laboratoire riva inc. | 02377861 | Powder For Solution - Oral | 20 MG / SACHET | 10/10/2013 |
| COLD STIX-EXTRA STRENGTH | pnp pharmaceuticals inc | 02368439 | Powder For Solution - Oral | 20 MG / 4.5 G | N/A |
| CALDOMINE DH ADULTE | technilab pharma inc. | 00550485 | Liquid - Oral | 12.5 MG / 5 ML | 12/31/1981 |
| HOT LEMON RELIEF POWDER EXTRA STRENGTH | 02248704 | Powder - Oral | 20 MG / 22 G | N/A | |
| HOT LEMON RELIEF EXTRA STRENGTH | north pacific rim marketing inc. | 02239203 | Powder - Oral | 20 MG / 22 G | N/A |
| HOT LEMON REGULAR - PWR | prodemdis enr. | 02141833 | Powder
,
Package - Oral | 20 MG / PCK | 4/15/1997 |
| HOT LEMON COLD & SORE THROAT NIGHT | cellchem pharmaceuticals inc. | 02502488 | Powder - Oral | 20 MG / SACHET | N/A |
| NEOCITRAN EXTRA STRENGTH COLD & SINUS NIGHT - APPLE CINNAMON | haleon canada ulc | 02456982 | Powder For Solution - Oral | 20 MG / SACHET | 8/1/2017 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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