STANDARDIZED SENNA CONCENTRATE

N/A

Manufactured by Atlantis Consumer Healthcare, Inc.

46,972 FDA adverse event reports analyzed

Last updated: 2026-04-14

About STANDARDIZED SENNA CONCENTRATE

STANDARDIZED SENNA CONCENTRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Atlantis Consumer Healthcare, Inc.. The most commonly reported adverse reactions for STANDARDIZED SENNA CONCENTRATE include FATIGUE, CONSTIPATION, PAIN, HEADACHE, NAUSEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for STANDARDIZED SENNA CONCENTRATE.

Top Adverse Reactions

FATIGUE1,720 reports
CONSTIPATION1,317 reports
PAIN1,282 reports
HEADACHE1,118 reports
NAUSEA1,115 reports
OFF LABEL USE985 reports
DIARRHOEA971 reports
DYSPNOEA944 reports
PNEUMONIA921 reports
PYREXIA920 reports
DRUG INEFFECTIVE860 reports
VOMITING825 reports
DEATH816 reports
ASTHENIA810 reports
BACK PAIN761 reports
HYPERHIDROSIS731 reports
RASH698 reports
DIZZINESS693 reports
MALAISE640 reports
FALL624 reports
HYPERTENSION591 reports
ABDOMINAL PAIN588 reports
ASTHMA564 reports
FLUID RETENTION563 reports
UPPER RESPIRATORY TRACT INFECTION554 reports
ANXIETY545 reports
HYPERSENSITIVITY522 reports
INFUSION RELATED REACTION506 reports
RHEUMATOID ARTHRITIS496 reports
ABDOMINAL PAIN UPPER494 reports
DRUG HYPERSENSITIVITY490 reports
WEIGHT DECREASED487 reports
HEPATIC ENZYME INCREASED477 reports
SOMNOLENCE468 reports
ARTHRALGIA465 reports
THROMBOCYTOPENIA463 reports
DECREASED APPETITE458 reports
ANAEMIA455 reports
DEPRESSION455 reports
ERYTHEMA450 reports
IMMUNODEFICIENCY447 reports
JOINT SWELLING446 reports
COUGH437 reports
FOOD ALLERGY432 reports
RASH ERYTHEMATOUS428 reports
DEHYDRATION414 reports
PRODUCT USE ISSUE397 reports
URINARY TRACT INFECTION393 reports
GASTROOESOPHAGEAL REFLUX DISEASE388 reports
CONFUSIONAL STATE387 reports
OVERDOSE380 reports
PAIN IN EXTREMITY367 reports
EXPOSURE DURING PREGNANCY362 reports
OEDEMA PERIPHERAL353 reports
PRURITUS349 reports
INFECTION348 reports
TEMPERATURE REGULATION DISORDER346 reports
BURSITIS335 reports
HYPOTENSION333 reports
PRESCRIBED OVERDOSE333 reports
TREMOR329 reports
HAEMOGLOBIN DECREASED323 reports
COELIAC DISEASE316 reports
FEELING ABNORMAL315 reports
INTENTIONAL PRODUCT MISUSE311 reports
BRONCHITIS309 reports
CHEST PAIN306 reports
BLOOD PRESSURE INCREASED302 reports
PLEURAL EFFUSION301 reports
CONTRAINDICATED PRODUCT ADMINISTERED290 reports
HALLUCINATION286 reports
DRUG INTOLERANCE282 reports
INSOMNIA280 reports
PSORIASIS275 reports
FEBRILE NEUTROPENIA273 reports
DISEASE PROGRESSION270 reports
NEUTROPENIA256 reports
WEIGHT INCREASED253 reports
PNEUMONIA ASPIRATION250 reports
AGITATION249 reports
COMA247 reports
GAIT DISTURBANCE247 reports
PULMONARY EMBOLISM246 reports
CYSTITIS245 reports
SEPSIS245 reports
TREATMENT FAILURE244 reports
ACUTE KIDNEY INJURY243 reports
MALIGNANT NEOPLASM PROGRESSION237 reports
STOMATITIS234 reports
CONDITION AGGRAVATED233 reports
NASOPHARYNGITIS233 reports
MYOCARDIAL INFARCTION231 reports
MIGRAINE229 reports
PERIPHERAL SWELLING228 reports
HYPOAESTHESIA227 reports
VISION BLURRED226 reports
GENERAL PHYSICAL HEALTH DETERIORATION224 reports
PLATELET COUNT DECREASED221 reports
ABDOMINAL DISTENSION220 reports
MUSCULAR WEAKNESS219 reports

Report Outcomes

Out of 12,237 classified reports for STANDARDIZED SENNA CONCENTRATE:

Serious 85.6%Non-Serious 14.4%

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

Female6,696 (58.7%)
Male4,709 (41.3%)
Unknown10 (0.1%)

Reports by Age

Age 64353 reports
Age 58340 reports
Age 78247 reports
Age 68239 reports
Age 53237 reports
Age 70231 reports
Age 69227 reports
Age 67218 reports
Age 60215 reports
Age 73211 reports
Age 65200 reports
Age 72197 reports
Age 75197 reports
Age 71195 reports
Age 66191 reports
Age 76187 reports
Age 74186 reports
Age 77180 reports
Age 57169 reports
Age 59168 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 STANDARDIZED SENNA CONCENTRATE?

This profile reflects 46,972 FDA FAERS reports that mention STANDARDIZED SENNA CONCENTRATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for STANDARDIZED SENNA CONCENTRATE?

Frequently reported terms in FAERS include FATIGUE, CONSTIPATION, PAIN, HEADACHE, NAUSEA, OFF LABEL USE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures STANDARDIZED SENNA CONCENTRATE?

Labeling and FAERS entries often list Atlantis Consumer Healthcare, Inc. in connection with STANDARDIZED SENNA CONCENTRATE. 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.