Question:
An extension of the normal pharmacological effects of a drug or its metabolite is termed as..........
An extension of the normal pharmacological effects of a drug or its metabolite is termed as..........
Updated On: Jul 16, 2024
- Туре A ADR
- Type B ADR
- Type C ADR
- Type D ADR
Hide Solution
Verified By Collegedunia
The Correct Option is A
Solution and Explanation
The correct option is (A) : Туре A ADR
Was this answer helpful?
0
0
Top Questions on Bio-availability & Bio-equivalence
- Which type of in-vitro-in-vivo correlation compares % drug released vs % drug absorbed?
- GPAT - 2023
- Biopharmaceutics and Pharmacokinetics
- Bio-availability & Bio-equivalence
- Under which of the following conditions in-vitro-in-vivo correlation for a drug fails?
- GPAT - 2023
- Biopharmaceutics and Pharmacokinetics
- Bio-availability & Bio-equivalence
- Decrease in effective surface area available to the dissolution medium leading to a fall in the dissolution rate, may happen due to which one of the following reasons?
- GPAT - 2022
- Biopharmaceutics and Pharmacokinetics
- Bio-availability & Bio-equivalence
- Match List I with List II
List I List II A When two dosage forms have equal t max I When their total body clearance is constant. B AUC values of the two analogs can be compared to measure relative bioavailability II Absorption rate constants are equal C Urinary data is valid to measure bioavailability. III. W III When fraction absorbed and elimination rate is constant. D C max is proportional to the rate of absorption IV Excretion of drug and/or metabolite is related to the bioavailable dose. Choose the correct answer from the options given below:
- GPAT - 2022
- Biopharmaceutics and Pharmacokinetics
- Bio-availability & Bio-equivalence
- For solid oral drug products, a change in the concentration of which of the following excipients is more likely to influence the bioavailability of a drug.
- GPAT - 2021
- Biopharmaceutics and Pharmacokinetics
- Bio-availability & Bio-equivalence
View More Questions
Questions Asked in GPAT exam
- How much volume of Raw spirit can an excise officer withdraw as sample?
- GPAT - 2025
- Indian Pharmaceutical Industry- An Overview
- Match the following:
(1) Schedule FF
(2) Schedule F3
(3) Schedule V
(4) Schedule Y
Descriptions:
(P) Standards of patent and proprietary medicines
(Q) Requirements and guidelines for clinical trials
(R) Standards for sterilized umbilical tapes
(S) Standards for Ophthalmic preparations- GPAT - 2025
- Drug therapy
- Glycogenic amino acids enter TCA cycle except:
- GPAT - 2025
- Biochemistry
- Which of the following alkaloids are found as salts of meconic acid?
- GPAT - 2025
- Introductory Pharmacognosy
Match the following:
(P) Schedule H
(Q) Schedule G
(R) Schedule P
(S) Schedule F2
Descriptions:
(I) Life period of drugs
(II) Drugs used under RMP
(III) List of Prescription Drugs
(IV) Standards for surgical dressing
- GPAT - 2025
- Drug therapy
View More Questions