CANDIDA ALBICANS

N/A

Manufactured by DNA Labs, Inc.

1,258 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CANDIDA ALBICANS

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

Top Adverse Reactions

DIARRHOEA39 reports
FATIGUE38 reports
HEADACHE35 reports
PAIN34 reports
NAUSEA29 reports
ARTHRALGIA28 reports
DIZZINESS26 reports
GAIT DISTURBANCE24 reports
MALAISE23 reports
PAIN IN EXTREMITY22 reports
PRODUCT DOSE OMISSION ISSUE22 reports
ASTHENIA21 reports
FALL20 reports
FLUSHING20 reports
PRURITUS20 reports
VOMITING20 reports
ABDOMINAL PAIN UPPER19 reports
DEATH19 reports
DYSPNOEA19 reports
DRUG INEFFECTIVE18 reports
EYE PAIN18 reports
FEELING ABNORMAL18 reports
CONSTIPATION17 reports
MUSCLE SPASMS17 reports
OFF LABEL USE17 reports
ALOPECIA16 reports
BLOOD PRESSURE INCREASED16 reports
INSOMNIA16 reports
DEPRESSION15 reports
MULTIPLE SCLEROSIS RELAPSE15 reports
RASH15 reports
CONFUSIONAL STATE14 reports
PARAESTHESIA14 reports
PNEUMONIA14 reports
WEIGHT INCREASED14 reports
HYPOAESTHESIA13 reports
PERIPHERAL SWELLING13 reports
TREMOR13 reports
VISION BLURRED13 reports
WEIGHT DECREASED13 reports
DRUG DOSE OMISSION12 reports
PRODUCT SUBSTITUTION ISSUE12 reports
BACK PAIN11 reports
BALANCE DISORDER11 reports
MIGRAINE11 reports
VISUAL IMPAIRMENT11 reports
ABDOMINAL DISCOMFORT10 reports
INFLUENZA LIKE ILLNESS10 reports
PRODUCT DOSE OMISSION10 reports
SWELLING10 reports
URTICARIA10 reports
ANXIETY9 reports
CONDITION AGGRAVATED9 reports
CONTUSION9 reports
DECREASED APPETITE9 reports
ERYTHEMA9 reports
MULTIPLE SCLEROSIS9 reports
MUSCULOSKELETAL STIFFNESS9 reports
NEUROPATHY PERIPHERAL9 reports
PYREXIA9 reports
COVID 198 reports
GASTROINTESTINAL DISORDER8 reports
HOT FLUSH8 reports
JOINT SWELLING8 reports
MEMORY IMPAIRMENT8 reports
PALPITATIONS8 reports
SEIZURE8 reports
BLOOD GLUCOSE INCREASED7 reports
BURNING SENSATION7 reports
CHEST PAIN7 reports
CHILLS7 reports
DYSPEPSIA7 reports
HYPERSENSITIVITY7 reports
ILLNESS7 reports
INTENTIONAL PRODUCT MISUSE7 reports
MYALGIA7 reports
PRODUCT DOSE OMISSION IN ERROR7 reports
PRODUCT USE ISSUE7 reports
SINUSITIS7 reports
SLEEP DISORDER7 reports
SOMNOLENCE7 reports
AMNESIA6 reports
CHRONIC KIDNEY DISEASE6 reports
DRUG HYPERSENSITIVITY6 reports
DRUG INTOLERANCE6 reports
GASTROOESOPHAGEAL REFLUX DISEASE6 reports
MYOCARDIAL INFARCTION6 reports
NASOPHARYNGITIS6 reports
OROPHARYNGEAL PAIN6 reports
SKIN EXFOLIATION6 reports
SUICIDAL IDEATION6 reports
THERAPY CESSATION6 reports
THROMBOSIS6 reports
URINARY INCONTINENCE6 reports
ARTHRITIS5 reports
CATARACT5 reports
CEREBROVASCULAR ACCIDENT5 reports
CHEST DISCOMFORT5 reports
CONTRAINDICATED PRODUCT ADMINISTERED5 reports
COUGH5 reports

Report Outcomes

Out of 589 classified reports for CANDIDA ALBICANS:

Serious 55.7%Non-Serious 44.3%

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

Female405 (70.9%)
Male166 (29.1%)

Reports by Age

Age 6818 reports
Age 7018 reports
Age 6617 reports
Age 6516 reports
Age 7216 reports
Age 6415 reports
Age 5814 reports
Age 7514 reports
Age 6913 reports
Age 6712 reports
Age 7112 reports
Age 7411 reports
Age 7611 reports
Age 6110 reports
Age 8110 reports
Age 8210 reports
Age 529 reports
Age 599 reports
Age 739 reports
Age 478 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 CANDIDA ALBICANS?

This profile reflects 1,258 FDA FAERS reports that mention CANDIDA ALBICANS. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CANDIDA ALBICANS?

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

Who manufactures CANDIDA ALBICANS?

Labeling and FAERS entries often list DNA Labs, Inc. in connection with CANDIDA ALBICANS. 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.