![]() |
| Oseltamavir PFOS |
Oseltamivir is an antiviral medication used to treat and prevent influenza (flu) caused by influenza A and B viruses.
What does “PFOS” mean?
In medication labeling, PFOS usually refers to Oseltamivir Phosphate — the phosphate salt form of oseltamivir.
It improves the drug’s stability and absorption in the body.
⚠️ It is not related to the chemical pollutant PFOS (perfluorooctanesulfonic acid). In this context, it simply indicates the pharmaceutical salt form.
How it works
Oseltamivir is a neuraminidase inhibitor.
It blocks the influenza virus enzyme neuraminidase, which prevents the virus from spreading to healthy cells.
Best results occur when started:
Within 48 hours of flu symptom onset.
Common Uses
✔ Treatment of flu symptoms
✔ Prevention after exposure (e.g., family member with flu)
✔ Used in adults and children (dose depends on age/weight)
Typical Adult Dose
Treatment: 75 mg twice daily for 5 days
Prevention: 75 mg once daily for 7–10 days
Always follow a doctor’s prescription.
Possible Side Effects
Most common:
Nausea
Vomiting
Headache
Rare but serious:
Allergic reactions
Confusion or unusual behavior (mostly reported in children)
Important Notes
It does not cure the flu instantly.
It does not replace flu vaccination.
It is ineffective against common cold viruses.
Basic Information as per USP
-
Molecular formula (free base): C₁₆H₂₈N₂O₄
-
Molecular formula (phosphate salt – PFOS form marketed): C₁₆H₂₈N₂O₄ · H₃PO₄
-
Molecular weight (free base): 312.4 g/mol
-
Drug class: Neuraminidase inhibitor (antiviral)
Key Structural Features
-
Cyclohexene ring core
-
Ethyl ester group
-
Primary amine (–NH₂)
-
Secondary amine
-
Ether linkage
-
Acetamido group
The marketed form is oseltamivir phosphate, which is the phosphate salt of the active oseltamivir base.
Oseltamavir PFOS in usp
Oseltamivir phosphate in United States Pharmacopeia (USP)
In the USP–NF, the official monograph name is:
Oseltamivir Phosphate
It is listed as the phosphate salt of oseltamivir (not “PFOS” — the correct abbreviation in pharmacopeial context is simply oseltamivir phosphate).
📌 USP Monograph Key Information
Official Name: Oseltamivir Phosphate
Category: Antiviral agent
Dosage forms covered:
Capsules
Powder for Oral Suspension
🧪 USP Description (Summary)
Chemical name:
Ethyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate phosphate
Molecular formula:
C₁₆H₂₈N₂O₄ · H₃PO₄
Molecular weight:
410.40 g/mol
Structure: Oseltamivir base + phosphoric acid (1:1 salt)
🔬 USP Identification Tests Typically Include
Infrared (IR) spectroscopy
HPLC retention time comparison with USP Reference Standard
Phosphate identification test
📊 USP Assay Method (General)
Technique: HPLC
Acceptance criteria: Typically 98.0% – 102.0% (on anhydrous basis)
Impurities controlled per USP related substances test
📦 USP Reference Standard
USP provides:
Oseltamivir Phosphate RS
Used for:
Assay
Related substances
System suitability testing
Full USP monograph assay conditions (mobile phase, column, wavelength)
Impurity limits
Dissolution specifications for capsules
Comparison with Ph. Eur. or BP

Comments
Post a Comment
If you have any doubts, please let me know