The Ministry of
Health and Family Welfare, Government of India has recently prohibited the
manufacture for sale, sale or distribution for human use of 328 fixed dose combinations
(FDCs) with immediate effect, including FDCs in diabetes.
All of us have
read the Government’s notification on FDCs and it has generated some
confusion and also raised several questions as to what is allowed and what is
not allowed.
Let us talk
about the rationality of use of FDCs in diabetes.
Type 2 diabetes
is a progressive disease, characterized by insulin resistance and β-cell
dysfunction. As the disease runs its course, the initial oral hypoglycemic
agent (OHA) prescribed may lose its efficacy leading to inadequate glycemic
control, which requires sequential addition of a second or even a third drug
belonging to a different class of OHAs, to achieve target or desired glycemic
control.
Combination
therapy administered as separate medications may deter patient from adhering to
the prescribed treatment.
Combining two or
more OHAs as a single-dose fixed-dose combinations (FDCs) therefore improves
treatment adherence by minimizing medication burden to the patient and also
reduces costs of treatment, which is a very important consideration, given that
out of pocket expenditure on health is amongst the highest in India.
A widely used
FDC in diabetes is the combination of glimepiride, metformin and pioglitazone
in two strengths: lower strength (7.5 mg) & higher strength (15 mg).
Triple drug
combinations reduced A1c to a greater extent than two drugs in a systematic
review and meta-analysis of randomized controlled trials, which examined the
addition of a third agent after dual therapy failure in
patients inadequately controlled with two agents (predominantly metformin and a
sulfonylurea or metformin and a thiazolidinedione),. In trials lasting 52 to 54
weeks, addition of thiazolidinediones, GLP-1 receptor agonists, or SGLT2
inhibitors to metformin and sulfonylurea reduced A1c to a similar extent (Diabetes
Obes Metab. 2018 Apr;20(4):985-997).
It is important
to note that the Govt. notification also says, “It has also “restricted” the
manufacture, sale or distribution of six FDCs“subject to certain
conditions”.
The Govt. of
India’s notification has recommended the discontinuation of only the FDCs
containing lower strength of pioglitazone because of inadequate
published international literature, but has allowed the FDC of
glimepiride and metformin with pioglitazone in higher strength (15mg).
The notification
has not questioned the safety and efficacy of the three molecules. The only
issue raised is use of a particular strength of the molecule.
Anti-diabetic triple
FDCs containing glimepiride, metformin with high dose
pioglitazone are approved by DCGI and all patients can be
continued on the existing medication.
In
case a patient happens to be on the FDC containing the lower strength
of pioglitazone (7.5mg), he should be evaluated again.
Status of FDCs
for diabetes
Strength
|
Status
|
Glimepiride (1mg/2mg) + Pioglitazone (15mg) + Metformin
500mg (Immediate Release/Sustained Release/ Extended Release) Tablet
|
Allowed
|
Pio
7.5 + Met 500/1000
|
Prohibited
|
Glimepiride
1/2/3 + Pio 15 + Met 1000
|
Prohibited
|
Glimepiride
1mg/ 2mg + Pioglitazone 15mg/ 15mg + Metformin 850mg/ 850mg v
|
Prohibited
|
Metformin
850mg + Pioglitazone 7.5 mg + Glimepiride 2mg
|
Prohibited
|
Metformin
850mg + Pioglitazone 7.5 mg + Glimepiride 1mg
|
Prohibited
|
Metformin
500mg/ 500mg + Gliclazide SR 30mg/ 60mg + Pioglitazone 7.5mg/ 7.5mg
|
Prohibited
|
Voglibose
+ Pioglitazone + Metformin
|
Prohibited
|
Pioglitazone
30 mg + Metformin 500 mg
|
Prohibited
|
Pioglitazone
15 mg + Metformin 850 mg
|
Prohibited
|
Metformin
+ Gliclazide + Pioglitazone + Chromium Polynicotinate
|
Prohibited
|
Metformin (sustained release) 500mg + Pioglitazone 15 mg + Glimepride 3mg
|
Prohibited
|
Metformin
(SR) 500mg + Pioglitazone 5mg
|
Prohibited
|
The relevant
section of the notification is reproduced as below:
NOTIFICATION
New Delhi, the 7th September, 2018
S.O.
4711(E).—Whereas, the Central Government in exercise of the powers conferred by
section 26 A of the Drugs and Cosmetics Act, 1940 (23 of 1940) prohibited the
manufacture for sale, sale and distribution for human use of drug fixed dose
combination of Glimepiride + Pioglitazone + Metformin vide S.O.
number 815 (E) published in the Gazette of India: Extraordinary Part II-
Section 3(ii), Dated the 10th March, 2016;
And
whereas, in compliance with the directions given by the Supreme Court of
India in its judgement dated the 15th December, 2017 in Union of India and
Anr. v/s Pfizer Ltd. and Ors. Civil Appeal No. 22972 of 2017 (Arising out of
SLP (c) No.7061 of 2017), the matter was examined by Drugs Technical Advisory
Board constituted under section 5 of the Drugs and Cosmetics Act, 1940 (23 of
1940) which furnished its report on the 31st July, 2018 in respect of above
drug to the Central Government.
And
whereas, the Drugs Technical Advisory Board recommended that “FDC ofGlimepiride
+ Pioglitazone + Metformin may be restricted under section 26A for
the following strengths: 1. Glimepiride (1mg/2mg) + Pioglitazone
(15mg) + Metformin 500mg (Immediate Release/Sustained Release/
Extended Release) Tablet for "Treatment of type-2 diabetes mellitus
(T2DM) when diet, exercise along with monotherapy and dual therapy does not
achieve glycaemic target" as this FDC with the said strengths is
'rational' for the defined patient population. Further, the label and all the
promotional literature including the package insert shall mention the
precautions for individual drugs. Any other strength of FDC of Glimepiride
+ Pioglitazone + Metformin except above mentioned strengths is not
recommended”.
Now,
therefore, in supersession of the notification of the Government of India,
Ministry of Health and Family Welfare (Department of Health and Family
Welfare) published in the Gazette of India, Extraordinary, Part II, Section
3, Sub-section (ii), vide number S.O. 815 (E) dated the 10th March,
2016 and in exercise of the powers conferred by section 26A of the Drugs and
Cosmetics Act, 1940 the Central Government hereby, restricts the manufacture,
sale or distribution of the drug Fixed Dose Combination of Glimepiride
+ Pioglitazone + Metformin subject to the following conditions,-
(i)
the manufacture, sale or distribution of the said drug shall be in the
strength of Glimepiride (1mg/2mg) + Pioglitazone (15mg) + Metformin 500mg
(Immediate Release or Sustained Release or Extended Release) Tablet only;
(ii)
the said drug shall be used for treatment of type-2 diabetes mellitus (T2DM)
when diet, exercise along with monotherapy and dual therapy does not achieve
glycaemic target; and
(iii)
in respect of the said drug, the label and all the promotional literature
including the package insert shall mention the precautions for individual
drugs respectively.
This
notification shall come into force with immediate effect.
[F. No. X.11035/53/2014-DFQC (Pt. II)]
SUDHIR KUMAR, Jt. Secy.
|
Dr KK Aggarwal
Padma
Shri Awardee
Vice
President CMAAO
Group
Editor-in-Chief IJCP Publications
President
Heart Care Foundation of India
Immediate Past National President IMA
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