AGNUS CASTUS

N/A

Manufactured by Boiron

146 FDA adverse event reports analyzed

Last updated: 2026-04-15

About AGNUS CASTUS

AGNUS CASTUS is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for AGNUS CASTUS include ABDOMINAL DISTENSION, ABDOMINAL PAIN UPPER, CHEST PAIN, NAUSEA, ABDOMINAL PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for AGNUS CASTUS.

Top Adverse Reactions

ABDOMINAL DISTENSION6 reports
ABDOMINAL PAIN UPPER6 reports
CHEST PAIN6 reports
NAUSEA6 reports
ABDOMINAL PAIN5 reports
ACNE CYSTIC5 reports
ALOPECIA5 reports
BACK PAIN5 reports
CONSTIPATION5 reports
DIARRHOEA5 reports
DYSPEPSIA5 reports
COVID 193 reports
DIZZINESS3 reports
DYSPNOEA3 reports
ERYTHEMA2 reports
FOETAL EXPOSURE DURING PREGNANCY2 reports
HEADACHE2 reports
HYPOAESTHESIA2 reports
NASOPHARYNGITIS2 reports
PAIN IN EXTREMITY2 reports
PARAESTHESIA2 reports
RESPIRATORY SYNCYTIAL VIRUS INFECTION2 reports
VAGINAL HAEMORRHAGE2 reports
VISUAL IMPAIRMENT2 reports
WEIGHT DECREASED2 reports
ACNE PUSTULAR1 reports
AGEUSIA1 reports
ANXIETY1 reports
ARTHRALGIA1 reports
ASCITES1 reports
BRADYCARDIA FOETAL1 reports
CARDIAC DISORDER1 reports
CARDIOVASCULAR INSUFFICIENCY1 reports
CIRCULATORY COLLAPSE1 reports
COUGH1 reports
DECREASED APPETITE1 reports
DEPRESSION1 reports
DRUG EXPOSURE DURING PREGNANCY1 reports
DRUG INEFFECTIVE1 reports
DRUG INTERACTION1 reports
DYSMENORRHOEA1 reports
DYSSTASIA1 reports
EXPOSURE DURING PREGNANCY1 reports
EXPOSURE VIA BREAST MILK1 reports
EYE PAIN1 reports
GASTROINTESTINAL INFECTION1 reports
GESTATIONAL DIABETES1 reports
HUMAN PAPILLOMA VIRUS TEST POSITIVE1 reports
HYPOGLYCAEMIA1 reports
HYPOTONIA1 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION1 reports
INJECTION SITE ERYTHEMA1 reports
INJECTION SITE PAIN1 reports
INJECTION SITE SWELLING1 reports
IRON DEFICIENCY1 reports
JAUNDICE1 reports
LIVER FUNCTION TEST ABNORMAL1 reports
MENTAL DISORDER1 reports
MONOPLEGIA1 reports
MUCOSAL INFLAMMATION1 reports
MUSCLE SPASMS1 reports
NEONATAL RESPIRATORY DISTRESS1 reports
OFF LABEL USE1 reports
OSTEOCHONDROSIS1 reports
OVARIAN HYPERSTIMULATION SYNDROME1 reports
PALLOR1 reports
PELVIC PAIN1 reports
PLEURAL EFFUSION1 reports
PREGNANCY ON ORAL CONTRACEPTIVE1 reports
PREMATURE BABY1 reports
SHOCK1 reports
SKIN DISCOLOURATION1 reports
SPINAL PAIN1 reports
SUICIDAL IDEATION1 reports
SUSPECTED COUNTERFEIT PRODUCT1 reports
SYNCOPE1 reports
TETANY1 reports
THERAPEUTIC RESPONSE UNEXPECTED1 reports
UNINTENDED PREGNANCY1 reports
UPPER RESPIRATORY TRACT INFECTION1 reports
URINARY TRACT INFECTION1 reports

Report Outcomes

Out of 23 classified reports for AGNUS CASTUS:

Serious 78.3%Non-Serious 21.7%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female22 (100.0%)

Reports by Age

Age 224 reports
Age 02 reports
Age 322 reports
Age 332 reports
Age 181 reports
Age 231 reports
Age 301 reports
Age 311 reports
Age 341 reports
Age 351 reports
Age 361 reports
Age 381 reports
Age 441 reports
Age 451 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with AGNUS CASTUS?

This profile reflects 146 FDA FAERS reports that mention AGNUS CASTUS. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for AGNUS CASTUS?

Frequently reported terms in FAERS include ABDOMINAL DISTENSION, ABDOMINAL PAIN UPPER, CHEST PAIN, NAUSEA, ABDOMINAL PAIN, ACNE CYSTIC. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures AGNUS CASTUS?

Labeling and FAERS entries often list Boiron in connection with AGNUS CASTUS. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.