Hi, help us enhance your experience
Hi, help us enhance your experience
Hi, help us enhance your experience
590 Views
eMediNexus 09 January 2023
If a patient suffers an adverse drug reaction while on treatment, the doctor is required to disclose the information under the Pharmacovigilance Programme of India.
If there is any suspicion that an adverse event or an adverse reaction has occurred, the healthcare professional attending to the patient can report the adverse drug reactions (ADR) in a prescribed form to the ADRs Monitoring Centers under the Pharmacovigilance Programme of India (PvPI).
Only the patient’s initials have to be filled in the ADR form and all the patient details are kept confidential. The form can be downloaded from the websites of Indian Pharmacopoeia Commission (www.ipc.gov.in) or Central Drugs Standard Control Organization (CDSCO) (www.cdsco.nic.in).
{{Article_Title}}
{{Article_Author}}
{{Article_Title}}
{{Article_Author}}
{{Article_Title}}..
High 1-hour Plasma Glucose: Early Indicator of Type 2 Diabetes Risk..
Maintaining Liver Health to Optimize Glycemic Outcomes in Early Type 2.....
Hidden Hazard of Indoor Pollution in COPD..
Antibiotic Prescribing Practices for Pediatric Acute Otitis Media..
Recognizing Pitfalls of Point-of-Care Lung Ultrasound..
{{Article_Title}}..
HMPV in India: Seven Cases Reported across Four States..
West Bengal Commission Fines Divine Nursing Home Rs 10 Lakh for Medical Negligence..
India Reports First Human Metapneumovirus (HMPV) Cases in Karnataka..
Two-Year-Old Dies after Wrong Injection Administered by Private Compounder in Jaisalmer..
'Law of the Land' Paramount for Blinkit's Ambulance Services, Says PiyushGoyal..