DrugCite
Search

DESMOPRESSIN ACETATE

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Desmopressin Acetate Adverse Events Reported to the FDA Over Time

How are Desmopressin Acetate adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Desmopressin Acetate, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Desmopressin Acetate is flagged as the suspect drug causing the adverse event.

Most Common Desmopressin Acetate Adverse Events Reported to the FDA

What are the most common Desmopressin Acetate adverse events reported to the FDA?

Hyponatraemia
289 (7.38%)
Convulsion
108 (2.76%)
Vomiting
87 (2.22%)
Drug Ineffective
85 (2.17%)
Nausea
75 (1.91%)
Headache
71 (1.81%)
Confusional State
65 (1.66%)
Fall
53 (1.35%)
Blood Sodium Decreased
50 (1.28%)
Water Intoxication
44 (1.12%)
Drug Interaction
43 (1.1%)
Show More Show More
Loss Of Consciousness
40 (1.02%)
Coma
39 (1%)
Dizziness
38 (.97%)
Overdose
38 (.97%)
Off Label Use
37 (.94%)
Brain Oedema
35 (.89%)
Abdominal Pain
34 (.87%)
Drug Effect Decreased
31 (.79%)
Pyrexia
30 (.77%)
Hypernatraemia
29 (.74%)
Hypokalaemia
29 (.74%)
Hallucination
27 (.69%)
Inappropriate Antidiuretic Hormone ...
27 (.69%)
Agitation
25 (.64%)
Disorientation
25 (.64%)
Malaise
24 (.61%)
Dyspnoea
23 (.59%)
Medication Error
23 (.59%)
Grand Mal Convulsion
22 (.56%)
Lethargy
22 (.56%)
Epilepsy
21 (.54%)
Pain
21 (.54%)
Thirst
21 (.54%)
Diarrhoea
20 (.51%)
Electrolyte Imbalance
20 (.51%)
Fatigue
20 (.51%)
Condition Aggravated
19 (.49%)
Flushing
19 (.49%)
Dehydration
18 (.46%)
Hypotension
18 (.46%)
Depressed Level Of Consciousness
17 (.43%)
Psychotic Disorder
17 (.43%)
Amnesia
16 (.41%)
Asthenia
16 (.41%)
Balance Disorder
16 (.41%)
Depression
15 (.38%)
Hypertension
15 (.38%)
Myocardial Infarction
15 (.38%)
Petechiae
15 (.38%)
Pollakiuria
15 (.38%)
Tremor
15 (.38%)
Anorexia
14 (.36%)
Blood Pressure Increased
14 (.36%)
Chills
14 (.36%)
Pulmonary Embolism
14 (.36%)
Incorrect Dose Administered
13 (.33%)
Somnolence
13 (.33%)
Blood Creatine Phosphokinase Increa...
12 (.31%)
Chest Discomfort
12 (.31%)
Dry Mouth
12 (.31%)
Hyperhidrosis
12 (.31%)
Intestinal Ischaemia
12 (.31%)
Rash
12 (.31%)
Rhabdomyolysis
12 (.31%)
Therapeutic Response Unexpected Wit...
12 (.31%)
Urine Output Increased
12 (.31%)
Disturbance In Attention
11 (.28%)
Incontinence
11 (.28%)
Vision Blurred
11 (.28%)
Abdominal Pain Upper
10 (.26%)
Abnormal Behaviour
10 (.26%)
Anxiety
10 (.26%)
Bladder Cancer
10 (.26%)
Blood Potassium Decreased
10 (.26%)
Blood Sodium Increased
10 (.26%)
Diabetes Insipidus
10 (.26%)
Epistaxis
10 (.26%)
Hyperacusis
10 (.26%)
Memory Impairment
10 (.26%)
Migraine
10 (.26%)
Oedema Peripheral
10 (.26%)
Weight Increased
10 (.26%)
Arterial Thrombosis
9 (.23%)
Cerebrovascular Accident
9 (.23%)
Chest Pain
9 (.23%)
Eye Infection
9 (.23%)
Kidney Infection
9 (.23%)
Muscular Weakness
9 (.23%)
Restlessness
9 (.23%)
Sleep Terror
9 (.23%)
Thrombosis
9 (.23%)
Vena Cava Thrombosis
9 (.23%)
Aggression
8 (.2%)
Altered State Of Consciousness
8 (.2%)
Blood Chloride Decreased
8 (.2%)
Blood Osmolarity Decreased
8 (.2%)
Blood Pressure Decreased
8 (.2%)
Cognitive Disorder
8 (.2%)
Constipation
8 (.2%)
Deep Vein Thrombosis
8 (.2%)

ExportShare/Embed GraphExport Export Data

This graph shows the top adverse events submitted to the FDA for Desmopressin Acetate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Desmopressin Acetate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Desmopressin Acetate

What are the most common Desmopressin Acetate adverse events reported to the FDA?

Show More Show More

ExportShare/Embed Graph Export Export Data

This graph shows the top categories of adverse events submitted to the FDA for Desmopressin Acetate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Desmopressin Acetate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Desmopressin Acetate According to Those Reporting Adverse Events

Why are people taking Desmopressin Acetate, according to those reporting adverse events to the FDA?

Diabetes Insipidus
383
Enuresis
220
Drug Use For Unknown Indication
104
Hypopituitarism
66
Product Used For Unknown Indication
64
Blood Antidiuretic Hormone Decrease...
62
Show More Show More
Nocturia
59
Von Willebrands Disease
40
Urinary Incontinence
31
Ill-defined Disorder
27
Bladder Disorder
25
Hormone Replacement Therapy
15
Diabetes Mellitus
12
Pollakiuria
11
Antidiuretic Hormone Abnormality
10
Micturition Urgency
9
Incontinence
9
Hypothalamo-pituitary Disorder
8
Prophylaxis
8
Coagulopathy
8
Haemorrhage
7
Hypertonic Bladder
7
Bleeding Time Prolonged
5
Dental Implantation
5
Hypernatraemia
5
Oliguria
5
Blood Antidiuretic Hormone Abnormal
5
Pain
5
Polyuria
5
Supplementation Therapy
4
Urinary Tract Disorder
4
Platelet Disorder
4
Haemorrhage Prophylaxis
4
Hypophysectomy
4
Stress Urinary Incontinence
4
Secondary Hypothyroidism
3
Epilepsy
3
Analgesia
3
Electrolyte Imbalance
3
Bladder Prolapse
2
Renal Disorder
2
Vaginal Haemorrhage
2
Renal Failure
2
Cystitis Interstitial
2
Nephrogenic Diabetes Insipidus
2
Benign Prostatic Hyperplasia
2
Haemostasis
2
Hypophysitis
2
Off Label Use
2
Azotaemia
2
Urine Output Increased
2

Drug Labels

LabelLabelerEffective
Ddavpsanofi-aventis U.S. LLC01-SEP-09
Ddavpsanofi-aventis U.S. LLC01-SEP-09
Desmopressin AcetateAmerican Health Packaging14-DEC-09
Desmopressin AcetateUDL Laboratories, Inc.09-JUL-10
Desmopressin AcetateFerring Pharmaceuticals Inc.25-OCT-10
Desmopressin AcetatePhysicians Total Care, Inc.12-JAN-11
Desmopressin AcetateNCS HealthCare of KY, Inc dba Vangard Labs18-FEB-11
Desmopressin AcetatePhysicians Total Care, Inc.18-FEB-11
Desmopressin AcetateWatson Laboratories, Inc.20-JUN-11
Desmopressin AcetateHospira, Inc.21-JUL-11
Desmopressin AcetateWatson Laboratories, Inc.11-AUG-11
StimateCSL Behring LLC16-SEP-11
Desmopressin AcetateFerring Pharmaceuticals Inc.13-DEC-11
Desmopressin AcetateApotex Corp.07-MAR-12
Desmopressin AcetateFerring Pharmaceuticals Inc.31-MAR-12
Ddavpsanofi-aventis U.S. LLC09-APR-12
Desmopressin AcetateBauch & Lomb Incorporated13-APR-12
Desmopressin AcetateSun Pharmaceutical Industries Limited 14-APR-12
Ddavp Rhinal Tubesanofi-aventis U.S. LLC19-JUL-12
Desmopressin AcetateTeva Pharmaceuticals USA Inc02-AUG-12
Desmopressin AcetateTeva Parenteral Medicines, Inc.07-SEP-12
Desmopressin AcetateAmerican Health Packaging08-OCT-12
Desmopressin AcetateBryant Ranch Prepack18-JAN-13
Desmopressin AcetateSun Pharmaceutical Industries Limited 30-JAN-13
Desmopressin Acetate AvKARE, Inc.07-MAR-13
Desmopressin AcetateApotex Corp.09-APR-13

Desmopressin Acetate Case Reports

What Desmopressin Acetate safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Desmopressin Acetate. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

Comments

Share your experience with Desmopressin Acetate.