Welcome to our Adverse Event Reporting page. Please read the following to know how we process complaints and use the information provided by you in the subsequent "Complaints" form. Dissatisfactions and AE reports are typically forwarded to our company, headquartered in Mumbai, India for appropriate action while personal data submitted through the form is dealt with as per international norm/s which is clearly mentioned in our Privacy Policy. You can view the same HERE.

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Drug Safety &
Pharmacovigilance System

 

Archerchem was built upon the foundation of providing "Quality" drug and therapeutic biologic products, and continues to take this initiative seriously. It is the only reason why we not only support Adverse Event Reporting System (AERS), a monitoring watchdog for approved drugs, but wholeheartedly maintain a systematic event reporting database. We imbibe international drug laws out of ethics and not just to fulfill our global compliance regulation obligation.

Affected patients, medical professionals and peers are requested to fill the form in case of adverse effect / reaction post drug consumption.

Your feedback on these events helps us improve our products in terms of benefit to risk ratio.

 

Nature of event (Check all that apply) *
Patient Information
Sex *
Event Description
Current Status / Outcome: (at the time of this report) *
Drug Use Detail
Treatment Dates

Start Date *

End Date *

Expiry Date *

Reporter Information
Sex *

 

Types of adverse reaction reporting -

Users need to understand that an adverse reaction is a medical event where the consumption of drug has resulted in side effects, allergic reactions, overdose or negative experiences. The product has to be recalled in case the subsequent investigation does turn out to be true.

What needs to be reported?

Side effects and adverse reactions after consuming Archerchem medicines can be reported by actual patients or healthcare professionals.

Apart from the above situations, users and healthcare professionals can also report to Archerchem and Pharmacovigilance department for the below mentioned medical events.

  1. Reactions in a pregnant woman after consuming Archerchem drug >> Report to Pharmacovigilance department as pregnancy.
  2. Ineffective drug complaint >> Report to Pharmacovigilance department as Lack of efficacy.
  3. Overdose on drug consumption ( Archerchem ) >> Report to Pharmacovigilance department as overdose.
  4. Damaged packaging, discoloration or shapeless contents / broken tablets >> Report as Product Complaint.
  5. As a consumer or a healthcare professional you still wish to complaint in spite of AE ( Adverse Reaction Warning ) already mentioned on the packaging or forewarned by Archerchem's medical representative verbally? >> Report everything to Pharmacovigilance department

Who can report?

All end users / patients, healthcare professionals including doctors, nurses, pharmacists, and peers, friends and relatives of the affected individual.

Confidentiality -

The patient’s identity is held in strict confidence and never disclosed under any circumstances even if the request arises from a public platform.

If you would like to send us information by post, please download the form and mail to the following address:

Archerchem Healthcare Pvt. Ltd.
802, Advent Atria,
Opp. Kingston Complex,
Chincholi Bunder Road, Malad (W),
Mumbai - 400064, Maharashtra, India.

CALL US :+91 22 42361110 / +91 22 42361111