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HYPRHO D

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Hyprho D Adverse Events Reported to the FDA Over Time

How are Hyprho D adverse event reports trending over time?

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

Most Common Hyprho D Adverse Events Reported to the FDA

What are the most common Hyprho D adverse events reported to the FDA?

Drug Exposure During Pregnancy
134 (20.71%)
Adverse Event
91 (14.06%)
Metal Poisoning
87 (13.45%)
Neurotoxicity
73 (11.28%)
Autism
11 (1.7%)
Developmental Delay
10 (1.55%)
Nervous System Disorder
9 (1.39%)
Adenoidal Hypertrophy
8 (1.24%)
Attention Deficit/hyperactivity Dis...
8 (1.24%)
Bronchiolitis
8 (1.24%)
Croup Infectious
8 (1.24%)
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Interstitial Lung Disease
8 (1.24%)
Laryngeal Stenosis
8 (1.24%)
Otitis Media Chronic
8 (1.24%)
Viral Pharyngitis
8 (1.24%)
Anxiety
7 (1.08%)
Depression
7 (1.08%)
Headache
7 (1.08%)
Insomnia
7 (1.08%)
Meconium In Amniotic Fluid
7 (1.08%)
Stress
7 (1.08%)
Vaginitis Bacterial
7 (1.08%)
Hyperhidrosis
6 (.93%)
Condition Aggravated
5 (.77%)
Diarrhoea
5 (.77%)
Neurodevelopmental Disorder
5 (.77%)
Respiratory Tract Infection
5 (.77%)
Congenital Anomaly
4 (.62%)
Gastrointestinal Disorder
4 (.62%)
Immune System Disorder
4 (.62%)
Learning Disability
4 (.62%)
Abdominal Discomfort
3 (.46%)
Aversion
3 (.46%)
Blood Mercury Abnormal
3 (.46%)
Drug Ineffective
3 (.46%)
Dysphagia
3 (.46%)
Foetal Tobacco Exposure
3 (.46%)
Hearing Impaired
3 (.46%)
Stridor
3 (.46%)
Abnormal Behaviour
2 (.31%)
Adverse Drug Reaction
2 (.31%)
Aggression
2 (.31%)
Congenital Oral Malformation
2 (.31%)
Deafness
2 (.31%)
Encephalopathy
2 (.31%)
Exposure To Toxic Agent
2 (.31%)
Expressive Language Disorder
2 (.31%)
Forceps Delivery
2 (.31%)
Haematuria
2 (.31%)
Head Banging
2 (.31%)
Laboratory Test Abnormal
2 (.31%)
Maternal Drugs Affecting Foetus
2 (.31%)
Motor Dysfunction
2 (.31%)
Oppositional Defiant Disorder
2 (.31%)
Prolonged Labour
2 (.31%)
Screaming
2 (.31%)
Social Problem
2 (.31%)
Speech Disorder Developmental
2 (.31%)
Communication Disorder
1 (.15%)
Disturbance In Social Behaviour
1 (.15%)
Dyspnoea
1 (.15%)
Ear Infection
1 (.15%)
Fine Motor Delay
1 (.15%)
Injury
1 (.15%)
Nausea
1 (.15%)
Neonatal Aspiration
1 (.15%)
Neonatal Disorder
1 (.15%)
Nerve Root Injury
1 (.15%)
Neurological Symptom
1 (.15%)
Psychomotor Skills Impaired
1 (.15%)
Vacuum Extractor Delivery
1 (.15%)
Vomiting
1 (.15%)
Weight Decreased
1 (.15%)

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This graph shows the top adverse events submitted to the FDA for Hyprho D, 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 Hyprho D 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 Hyprho D

What are the most common Hyprho D adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Hyprho D, 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 Hyprho D 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 Hyprho D According to Those Reporting Adverse Events

Why are people taking Hyprho D, according to those reporting adverse events to the FDA?

Pregnancy
189
Rhesus Incompatibility
5
Drug Use For Unknown Indication
4

Hyprho D Case Reports

What Hyprho D safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Hyprho D. 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.

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