PECTIN

N/A

Manufactured by Mondelez Global LLC

356 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PECTIN

PECTIN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Mondelez Global LLC. The most commonly reported adverse reactions for PECTIN include FATIGUE, COUGH, DIARRHOEA, DRUG INEFFECTIVE, HEADACHE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PECTIN.

Top Adverse Reactions

FATIGUE14 reports
COUGH11 reports
DIARRHOEA11 reports
DRUG INEFFECTIVE9 reports
HEADACHE9 reports
NAUSEA8 reports
ABDOMINAL PAIN7 reports
ASTHENIA7 reports
DYSPNOEA7 reports
ANXIETY6 reports
BACK PAIN6 reports
FALL6 reports
PRURITUS6 reports
PYREXIA6 reports
BRONCHITIS5 reports
CHEST PAIN5 reports
DEHYDRATION5 reports
FEELING ABNORMAL5 reports
HYPERTENSION5 reports
MALAISE5 reports
ABDOMINAL DISTENSION4 reports
ARTHRALGIA4 reports
BLOOD PRESSURE INCREASED4 reports
CHOKING4 reports
CONDITION AGGRAVATED4 reports
CONFUSIONAL STATE4 reports
ERYTHEMA4 reports
INSOMNIA4 reports
MEMORY IMPAIRMENT4 reports
MUSCLE SPASMS4 reports
OFF LABEL USE4 reports
PAIN4 reports
PRODUCT USE ISSUE4 reports
TREMOR4 reports
WEIGHT DECREASED4 reports
ANAEMIA3 reports
BLOOD CREATININE INCREASED3 reports
CELLULITIS3 reports
CONSTIPATION3 reports
DEPRESSION3 reports
DIABETES MELLITUS3 reports
DIZZINESS3 reports
DRUG DOSE OMISSION3 reports
DRY SKIN3 reports
EMOTIONAL DISTRESS3 reports
GAIT DISTURBANCE3 reports
GASTROOESOPHAGEAL REFLUX DISEASE3 reports
HEART RATE INCREASED3 reports
HYPOKALAEMIA3 reports
HYPOMAGNESAEMIA3 reports
OROPHARYNGEAL PAIN3 reports
PERIPHERAL SWELLING3 reports
PNEUMONIA3 reports
PRODUCT DOSE OMISSION ISSUE3 reports
PRODUCT USE IN UNAPPROVED INDICATION3 reports
SOMNOLENCE3 reports
VISION BLURRED3 reports
VOMITING3 reports
ABDOMINAL DISCOMFORT2 reports
ABDOMINAL PAIN UPPER2 reports
AGITATION2 reports
ALOPECIA2 reports
ANAPHYLACTIC REACTION2 reports
ARRHYTHMIA2 reports
ASPARTATE AMINOTRANSFERASE INCREASED2 reports
BALANCE DISORDER2 reports
BLOOD CALCIUM DECREASED2 reports
BLOOD UREA INCREASED2 reports
BRADYPHRENIA2 reports
BURNING SENSATION2 reports
CARDIAC DISORDER2 reports
CHEST DISCOMFORT2 reports
CONJUNCTIVITIS2 reports
CONTUSION2 reports
COVID 192 reports
CROHN^S DISEASE2 reports
DEATH2 reports
DECREASED APPETITE2 reports
DEPRESSED LEVEL OF CONSCIOUSNESS2 reports
DRUG HYPERSENSITIVITY2 reports
DRY MOUTH2 reports
DYSPEPSIA2 reports
DYSPHAGIA2 reports
DYSPNOEA EXERTIONAL2 reports
EXPIRED DRUG ADMINISTERED2 reports
EYELID OEDEMA2 reports
FEEDING DISORDER2 reports
FINGER DEFORMITY2 reports
FLUID RETENTION2 reports
FLUSHING2 reports
FREQUENT BOWEL MOVEMENTS2 reports
GASTRIC DISORDER2 reports
GASTRITIS2 reports
GASTROINTESTINAL DISORDER2 reports
HALLUCINATION2 reports
HAND DEFORMITY2 reports
HYPERSOMNIA2 reports
HYPOTENSION2 reports
INCREASED TENDENCY TO BRUISE2 reports
INFLUENZA LIKE ILLNESS2 reports

Report Outcomes

Out of 123 classified reports for PECTIN:

Serious 72.4%Non-Serious 27.6%

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

Female78 (65.5%)
Male41 (34.5%)

Reports by Age

Age 629 reports
Age 614 reports
Age 784 reports
Age 583 reports
Age 663 reports
Age 693 reports
Age 703 reports
Age 32 reports
Age 62 reports
Age 202 reports
Age 362 reports
Age 512 reports
Age 532 reports
Age 542 reports
Age 562 reports
Age 682 reports
Age 712 reports
Age 772 reports
Age 802 reports
Age 812 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 PECTIN?

This profile reflects 356 FDA FAERS reports that mention PECTIN. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PECTIN?

Frequently reported terms in FAERS include FATIGUE, COUGH, DIARRHOEA, DRUG INEFFECTIVE, HEADACHE, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PECTIN?

Labeling and FAERS entries often list Mondelez Global LLC in connection with PECTIN. 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.