- Desmopressin Acetate
Drug Information
Ingredients:
Drug Brands and Names:
- Adiuretin Sd
- Concentraid
- Ddavp
- Ddavp (needs No Refrigeration)
- Desmogalen
- Desmopressin
- Desmopressin Acetate
- Desmopressin Acetate (needs No Refrigeration)
- Desmopressin Acetate Preservative Free
- Desmospray
- Desmotabs
- Minirin
- Nocutil
- Octostim
- Stimate
- Stimate (needs No Refrigeration)
Manufacturers:
- American Health Packaging
- Apotex Inc Richmond Hill
- Bedford Laboratories Div Ben Venue Laboratories Inc
- Csl Behring Llc
- Ferring Pharmaceuticals Inc
- Sanofi Aventis Us Llc
- Sanofi-aventis U.s. Llc
Approved Uses (Extracted from drug label):
- Atrophy
- Cystitis interstitial
- Delivery
- Diabetes insipidus
- Diabetes mellitus
- Enuresis
- Haemorrhage
- Hypophysectomy
- Infusion
- Injection
- Menorrhagia
- Nasal congestion
- Nephrogenic diabetes insipidus
- Nocturia
- Pollakiuria
- Polydipsia
- Polyuria
- Product used for unknown indication
- Rhinitis
- Sinus congestion
- Surgery
- Thought blocking
- Von willebrand's disease
Common Uses (Extracted from FDA adverse event reports):
- Diabetes insipidus (23%)
- Enuresis (18%)
- Product used for unknown indication (14%)
- Nocturia (6%)
- Von willebrand's disease (5%)
- Hypopituitarism (4%)
- Ill-defined disorder (3%)
- Urinary incontinence (3%)
- Hypertonic bladder (1%)
- Haemorrhage (1%)
- Nephrogenic diabetes insipidus (1%)
- Bladder disorder (1%)
- Incontinence (1%)
- Blood antidiuretic hormone decreased (1%)
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Desmopressin Acetate
Report is for all products sharing this active ingredient. Use the workbench for research on individual brands like Adiuretin Sd.- Official FDA
Reports - Social Media
Events (est.) - Total
Posts - Avg. Review
Score
Desmopressin Acetate Age and Gender Distribution (From AERS Data)
Trends in Desmopressin Acetate Adverse Event Reports
- AERS Reports (FDA)
- Social Media Reports
Desmopressin Acetate Adverse Event Reports (From AERS Data)
* Druginformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an official signal from the FDA or other regulatory entity.
Desmopressin Acetate Adverse Event Reports (From Social Media - User Reviews and Forum Discussions)
Comment on abnormal weight gain while taking desmopressin acetate (View full report on desmopressin acetate related abnormal weight gain)
Comment on weight decreased while taking desmopressin acetate (View full report on desmopressin acetate related weight decreased)
Comment on abdominal discomfort while taking desmopressin acetate (View full report on desmopressin acetate related abdominal discomfort)
Comment on dizziness while taking desmopressin acetate (View full report on desmopressin acetate related dizziness)
Comment on haemorrhage while taking desmopressin acetate (View full report on desmopressin acetate related haemorrhage)
Comment on hot flush while taking desmopressin acetate (View full report on desmopressin acetate related hot flush)
Comment on discomfort while taking desmopressin acetate (View full report on desmopressin acetate related discomfort)
Comment on headache while taking desmopressin acetate (View full report on desmopressin acetate related headache)
Comment on drug effect increased while taking desmopressin acetate (View full report on desmopressin acetate related drug effect increased)
Comment on incoherent while taking desmopressin acetate (View full report on desmopressin acetate related incoherent)
Common Side Effects of Desmopressin Acetate
* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.
* About AERS: The Adverse Event Reporting System (AERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into AERS. The AERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, AERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.
* About AERS: The Adverse Event Reporting System (AERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into AERS. The AERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, AERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.
The total number of adverse event reports in the FDA-owned Adverse Event Reporting System (AERS).
The total number of adverse event reports extracted from online social media sources (forum discussions, user reviews, etc).
The total number of distinct comments (forum posts, user reviews, etc) written by users of a drug.
The average review score.