Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Nifedipine
Drug ID BADD_D01566
Description Nifedipine, or BAY a 1040, is a first generation dihydropyridine L-type calcium channel blocker, similar to [nicardipine].[A190210,A190273,A175390,L11383] Nifedipine was developed by Bayer and first described in the literature, along with other dihydropyridines, in 1972.[A175390,A190276] Since nifedipine's development, second and third generation dihydropyridines have been developed with slower onsets and longer durations of action.[A190273] The most popular of the third generation dihydropyridines is [amlodipine].[A190273] Nifedipine was granted FDA approval on 31 December 1981.[L11383]
Indications and Usage Nifedipine capsules are indicated to treat vasospastic angina and chronic stable angina.[L11383] Extended release tablets are indicated to treat vasospastic angina, chronic stable angina, and hypertension.[L11389,L1245]
Marketing Status approved
ATC Code C08CA05
DrugBank ID DB01115
KEGG ID D00437
MeSH ID D009543
PubChem ID 4485
TTD Drug ID D04OSE
NDC Product Code 0904-7229; 46438-0635; 52932-0711; 0069-2670; 68981-039; 23155-194; 23155-195; 43826-031; 46708-732; 50090-1843; 50742-622; 51655-738; 55289-798; 62332-734; 68084-597; 68382-687; 68645-512; 68682-106; 70771-1365; 71335-0497; 48589-0006; 51927-0233; 0069-2660; 46708-734; 50742-261; 50742-262; 51407-624; 0228-2497; 60429-049; 62175-262; 62332-732; 68084-598; 70771-1192; 71610-055; 11014-0036; 11014-0341; 52133-0028; 60592-507; 50742-260; 59651-297; 68071-2619; 68382-688; 68645-603; 68682-108; 69315-211; 70771-1191; 70807-503; 71335-0744; 71335-1721; 71335-9651; 55154-4690; 68084-603; 70934-973; 11014-0035; 11014-0342; 48292-0034; 62991-1106; 43826-030; 46708-733; 50268-598; 50742-621; 51655-780; 55154-4157; 62175-261; 63629-9109; 68382-686; 68682-105; 70771-1366; 71610-689; 0904-7081; 0069-2650; 24979-009; 24979-011; 50268-599; 50742-620; 59651-295; 59651-296; 59762-1004; 67877-757; 68645-513; 68682-109; 71205-965; 71335-0489; 71610-290; 72162-1277; 38779-0280; 51927-5205; 65427-250; 71052-650; 51655-407; 51655-798; 60429-048; 62135-521; 67877-758; 68382-689; 70934-603; 71205-963; 71335-2132; 71610-144; 72214-503; 72789-219; 49452-4847; 52133-0009; 24979-010; 50268-597; 51655-386; 62135-523; 62175-260; 62332-733; 68382-685; 71205-412; 71335-1550; 71610-012; 0904-7082; 82920-709; 43826-032; 0228-2530; 53808-1118; 62135-522; 63187-875; 68682-107; 68788-7642; 68788-8164; 69315-212; 70518-2679; 70518-3520; 12527-0787; 0904-7208; 46438-0052; 60524-002; 50090-4158; 50090-5284; 50090-5328; 50090-6201; 50090-6450; 51655-990; 55154-8177; 67877-756; 68071-4411; 68382-690; 68645-604; 70771-1190; 70771-1367; 70934-963; 71205-964; 11014-0038; 51552-0720; 50090-4234; 50090-6203; 51407-622; 51407-623; 51655-593; 60429-047
UNII I9ZF7L6G2L
Synonyms Nifedipine | Bay-1040 | Bay 1040 | Bay1040 | BAY-a-1040 | BAY a 1040 | BAYa1040 | Cordipin | Cordipine | Corinfar | Korinfar | Nifangin | Nifedipine Monohydrochloride | Monohydrochloride, Nifedipine | Procardia | Procardia XL | Nifedipine-GTIS | Nifedipine GTIS | Vascard | Adalat | Fenigidin
Chemical Information
Molecular Formula C17H18N2O6
CAS Registry Number 21829-25-4
SMILES CC1=C(C(C(=C(N1)C)C(=O)OC)C2=CC=CC=C2[N+](=O)[O-])C(=O)OC
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Necrotising colitis07.08.01.0130.000075%Not Available
Respiratory tract congestion22.02.07.003--Not Available
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal stiffness15.03.05.027--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Infusion site pain12.07.05.002; 08.02.05.014--Not Available
Infusion site oedema12.07.05.013; 08.02.05.012--Not Available
Affect lability19.04.01.001--Not Available
Skin burning sensation23.03.03.021; 17.02.06.009--Not Available
Foetal death08.04.01.011; 18.01.02.0030.000336%
Haemorrhage24.07.01.0020.000261%Not Available
Palpable purpura24.12.04.018; 23.06.02.006; 10.02.02.019--Not Available
Vasodilation procedure25.03.01.001--Not Available
Disturbance in sexual arousal19.08.04.003--Not Available
Angiopathy24.03.02.007--Not Available
Urine output13.13.03.003--Not Available
Urine output increased13.13.03.002--Not Available
Hot flush24.03.01.005; 21.02.02.001; 08.01.03.027--
Neurological symptom17.02.05.010--Not Available
Adverse event08.06.01.010--Not Available
Allergic oedema08.01.07.014; 10.01.03.025--Not Available
Appetite disorder19.09.01.002; 14.03.01.004--Not Available
Breast disorder21.05.04.004--Not Available
Cardiac disorder02.11.01.003--Not Available
Connective tissue disorder10.04.04.026; 15.06.01.006--Not Available
Inflammation08.01.05.007; 10.02.01.0890.000112%Not Available
Ischaemic stroke24.04.06.010; 17.08.01.0180.000075%Not Available
Malnutrition14.03.02.004--Not Available
Mediastinal disorder22.09.03.001--Not Available
Mental disorder19.07.01.002--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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