Pharmaceutical Jurisprudence MCQ question and answer

21

If drug is so coloured, coated or polished that damage its therapeutic value or it is made to appear of better orgreater therapeutic value than it really is known as

A) Adulterated Drug B) Spurious Drug C) Misbranded Drug D) True Drug

Discuss

Answer & Solution

Answer: Option C

No explanation is given for this question. Let's Discuss on Board

22

What, is minimum space requirement for Manufacturing Asava / Arishta?

A) 150 sq. ft. B) 250 sq. ft. C) 200 sq. ft.. D) 100 sq. ft.

Discuss

Answer & Solution

Answer: Option C

No explanation is given for this question. Let's Discuss on Board

23

The Schedule in Drugs and Cosmetics Act that deals with the requirements and guidelines for clinical trials, import manufacture of new drugs is.

A) Schedule-O B) Schedule-M C) Schedule-F D) Schedule-Y

Discuss

Answer & Solution

Answer: Option D

No explanation is given for this question. Let's Discuss on Board

24

The name of the registered pharmacist can be removed from the register by the executive committee if it is found that

A) His name has been entered by error or an account of Mis representation or suppression of material fact B) He has been convicted of any offence or has been guilty of any infamous conduct and any professional respect C) Both A and B D) None of the above

Discuss

Answer & Solution

Answer: Option C

No explanation is given for this question. Let's Discuss on Board

25

Animal house is approved by

A) CLAA B) DCC C) CPCSEA D) DTAB

Discuss

Answer & Solution

Answer: Option C

No explanation is given for this question. Let's Discuss on Board

26

The Medicinal and Toilet Preparations (Excise Duties) Act came into force in

A) 1940 B) 1945 C) 1950 D) 1955

Discuss

Answer & Solution

Answer: Option D

No explanation is given for this question. Let's Discuss on Board

27

An original licence to sell drugs, unless sooner suspended or cancelled, shall be Valid for

A) Two years B) Three years C) Four years D) Five years

Discuss

Answer & Solution

Answer: Option D

No explanation is given for this question. Let's Discuss on Board

28

List of poisonous substances under Ayurvedic, Siddha and Unani medicines Schedule is

A) E(I) B) F C) F(I) D) F(III)

Discuss

Answer & Solution

Answer: Option A

No explanation is given for this question. Let's Discuss on Board

29

Production and control of opium is controlled by

A) Central Govt. B) State Govt. C) Individual States D) DCC

Discuss

Answer & Solution

Answer: Option A

No explanation is given for this question. Let's Discuss on Board

30

The Drugs and Magic Remedies (Objectionable Advertisements) Act was approved by the parliament in:

A) 1954 B) 1940 C) 1942 D) 1945

Discuss

Answer & Solution

Answer: Option A

Solution:

The correct answer is Option A: 1954.

Let's understand why this Act was needed:
Before 1954, many companies used to advertise drugs and certain 'magic remedies' with claims that were not true or were highly exaggerated.
For example, they might claim a product could cure serious diseases like cancer, diabetes, or even make someone taller, which was often misleading and dangerous.
These objectionable advertisements could trick people into buying products that didn't work and prevent them from seeking real medical treatment, putting their health at risk.

So, the Parliament approved The Drugs and Magic Remedies (Objectionable Advertisements) Act in 1954.
The main goal of this Act is to stop misleading advertisements for drugs and 'magic remedies'.
It makes sure that advertisements for health products are truthful and don't make false promises.
This law is crucial for public safety and consumer protection in the field of medicine.

Remember, knowing the year these important laws were passed helps you understand the history and development of pharmaceutical regulations!

Pharmaceutical Jurisprudence MCQ question and answer | Pharmacy MCQ question