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SK

HCP Connect Clinical Author

Dr. Simran Kohli

Infectious Diseases

Credentials: MBBS, MD (General Medicine), DM (Infectious Diseases)

Specialty

Infectious Diseases

Clinical Updates

19

Experience

4 Years

Author Biography

About Dr. Simran Kohli

Dr. Simran Kohli is an infectious-diseases physician with 4 years of clinical experience. She earned a DM in Infectious Diseases after an MD in General Medicine, focusing on antimicrobial stewardship and HIV care. She follows the challenge of antimicrobial resistance with particular concern. Her writing keeps clinicians updated on emerging infections and therapies.

WHO VSN Registry

Vaccine Safety Monographs

9 monographs

Clinical ReviewerUpdated Jan 5, 2026

Chickenpox (Varicella) Safety Monograph

Institutional safety information on varicella vaccines. Clinical data for Varivax and ProQuad, side effect profiles, and long-term surveillance metadata.

View Monograph
Primary AuthorUpdated Jan 5, 2026

COVID-19 Protocol Safety Monograph

Evidence-based safety protocols and clinical data for COVID-19 immunizations. Unified registry info from CDC and WHO sources.

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Clinical ReviewerUpdated Jan 5, 2026

Hepatitis B Safety Monograph

Comprehensive clinical safety data for Hepatitis B vaccines. Registry details for single-antigen and combination formulations, newborn protocols, and surveillance metadata.

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Clinical ReviewerUpdated Jan 5, 2026

MMR (Measles, Mumps, Rubella) Safety Monograph

Evidence-based safety information on MMR vaccines for measles, mumps, and rubella. Clinical safety data, side effects, and long-term surveillance metadata.

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Primary AuthorUpdated Jan 5, 2026

Meningococcal Safety Monograph

Professional safety data on MenACWY and MenB vaccines. Clinical trial outcomes, manufacturer packages (Menactra, Menveo, Bexsero), and long-term surveillance.

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Primary AuthorUpdated Jan 5, 2026

Mpox (Orthopoxvirus) Safety Monograph

Institutional safety information on Mpox (JYNNEOS) vaccines. Clinical safety data, side effects, risk-based eligibility, and monitoring protocols from CDC and WHO sources.

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Clinical ReviewerUpdated Jan 5, 2026

Pneumococcal Safety Monograph

Institutional safety data for pneumococcal vaccines (PCV13, PCV15, PCV20, PPSV23). Clinical monitoring, manufacturer profiles, and adverse event surveillance.

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Clinical ReviewerUpdated Jan 5, 2026

Shingles (Zoster) Safety Monograph

Institutional safety information on Shingrix and Zoster vaccines. Clinical data, reactogenicity profiles, and long-term surveillance metadata for adults 50+.

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Primary AuthorUpdated Jan 5, 2026

Smallpox (Biodefense) Safety Monograph

Institutional safety information on Smallpox (JYNNEOS, ACAM2000) vaccines. Clinical safety data, side effects, biodefense protocols, and monitoring.

View Monograph

Published Work

Recent Clinical Updates

19 articles

Infectious Disease

FDA Approves ZAYNICH for cUTI: 89.0% Test-of-Cure in Trial 1

FDA approves cefepime and zidebactam (ZAYNICH) for cUTI including pyelonephritis; Trial 1 showed 89.0% test‑of‑cure vs 68.4% with meropenem.

Sep 11, 2026|5 min read|Via PubMed

Infectious Disease

FDA Approves Rezafungin for Candidemia/IC: Day 30 Mortality 23.7% vs 21.3%

Rezafungin (REZZAYO) FDA-approved for candidemia and invasive candidiasis; ReSTORE Day 30 mortality 23.7% vs 21.3% supports once-weekly IV dosing for patients ≥12 yrs.

Sep 11, 2026|6 min read|Via FDA AccessData

Infectious Disease

Ciprofloxacin Guidance for Salmonella Infections and Resistance Considerations

Ciprofloxacin guidance for Salmonella infections: labeled indications, dosing for infectious diarrhea and typhoid fever, resistance data and safety considerations.

Sep 6, 2026|6 min read|Via DailyMed

Infectious Disease

FDA Approves Ensitrelvir (XOCOVA) for COVID-19 Post‑Exposure Prophylaxis: 67% Reduction in Confirmed Symptomatic COVID-19 in SCORPIO-PEP

Ensitrelvir (XOCOVA) approved for COVID-19 post-exposure prophylaxis; SCORPIO-PEP showed 67% reduction in confirmed symptomatic COVID-19 through Day 10.

Aug 28, 2026|6 min read|Via FDA AccessData

Infectious Disease

AREXVY Expanded for Adults 18–59 at Increased RSV Risk

AREXVY (respiratory syncytial virus vaccine, adjuvanted) expanded to include adults 18–59 at increased RSV LRTD risk; single 0.5 mL IM dose; safety includes local reactions and GBS...

Aug 24, 2026|6 min read|Via DailyMed

Infectious Disease

FDA Expands AREXVY to Adults 18–59 at Increased RSV Risk

AREXVY FDA expands indication to adults 18–59 at increased risk for RSV LRTD; prior adult data showed 82.6% LRTD risk reduction and 94.1% reduction for severe LRTD.

Aug 23, 2026|5 min read|Via FDA

Infectious Disease

FDA Approves zoliflodacin for Uncomplicated Urogenital Gonorrhea: 90.9% Microbiologic Cure

zoliflodacin uncomplicated urogenital gonorrhea: FDA approved Dec 12, 2025; single 3 g oral dose; microbiological cure 90.9% vs 96.2% in Trial 1.

Aug 20, 2026|6 min read|Via FDA AccessData

Infectious Disease

FDA Approves doravirine/islatravir for Virologically Suppressed HIV‑1: 1% ≥50 copies/mL

FDA approves doravirine/islatravir (IDVYNSO) for virologically suppressed HIV‑1 in adults; Week 48 trials showed 1% with HIV‑1 RNA ≥50 copies/mL in IDVYNSO arms.

Aug 14, 2026|6 min read|Via FDA AccessData

Infectious Disease

REVIVE: Fluvoxamine Reduces Fatigue Severity (−0.43 FSS) vs Placebo

Fluvoxamine long COVID fatigue: REVIVE trial found −0.43 mean FSS reduction vs placebo at day 60; sustained at day 90 (NCT06128967).

Jul 20, 2026|5 min read|Via PubMed

Infectious Disease

Nirmatrelvir/Ritonavir Cuts Hospitalization Risk 89% in EPIC-HR

Nirmatrelvir/ritonavir (PAXLOVID) reduced Covid-19 hospitalization/death risk by ~89% in EPIC-HR. Key efficacy, safety, dosing, and prescribing considerations for clinicians.

Jul 18, 2026|6 min read|Via PubMed

Infectious Disease

FDA Approves zoliflodacin for Gonorrhea: 90.9% Cure Rate

zoliflodacin (NUZOLVENCE) FDA approval for uncomplicated urogenital gonorrhea: 90.9% microbiologic cure vs 96.2% with ceftriaxone+azithromycin in Trial 1

Jul 16, 2026|5 min read|Via DailyMed

Infectious Disease

FDA Approves IDVYNSO for Suppressed HIV-1: 1% ≥50 copies/mL

IDVYNSO (doravirine/islatravir) FDA approval for virologically suppressed HIV-1; 1% with HIV-1 RNA ≥50 copies/mL at Week 48 in pivotal trials. doravirine islatravir HIV-1

Jul 12, 2026|4 min read|Via FDA (Prescribing Information)

Infectious Disease

FDA Approves Ensitrelvir for COVID-19 Postexposure Prophylaxis: 67% Reduction in SCORPIO-PEP

Ensitrelvir (XOCOVA) FDA approval for COVID-19 post-exposure prophylaxis: 67% reduction in symptomatic infection in SCORPIO-PEP (adults/adolescents 12+).

Jul 11, 2026|5 min read|Via PubMed

Infectious Disease

WHO's 2026 Guidelines: A Comprehensive Approach to Combatting Antimicrobial Resistance

Explore WHO's 2026 guidelines on antimicrobial resistance, focusing on surveillance, infection control, and research investment.

Apr 24, 2026|1 min read|Via The Lancet

Medical Research

Improve Ovarian Cancer Detection with Personalized Risk Score

Enhance patient outcomes with a cost-effective tool that combines blood test results and age for accurate ovarian cancer detection in women over 50.

Apr 20, 2026|3 min read|Via Medical Xpress

Digital Health

Automate 90% of Intake Workflows with AI

Discover how AI-powered automation can streamline post-acute care workflows, freeing staff to focus on patient care and reducing administrative burdens.

Apr 14, 2026|2 min read|Via HIT Consultant

Medical Research

Plant-Based Diet Cuts Type 2 Diabetes Risk

Discover how a plant-based diet can lower type 2 diabetes risk while reducing greenhouse gas emissions, benefiting both human and planetary health.

Apr 8, 2026|3 min read|Via Medical Xpress

Digital Health

Stay Ahead with Daily Digital Health Updates

Get the latest digital health news, trends, and insights to enhance patient care and stay informed about industry developments and innovations.

Apr 5, 2026|4 min read|Via Digital Health News

Medical Research

Reuse Patient Studies to Cut Drug Dev Costs

Discover how reusing existing patient preference studies can optimize resource allocation and streamline drug development processes, reducing costs and improving efficiency.

Mar 24, 2026|2 min read|Via Medical Xpress