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TAGRISSO 40 MG COMPRIMIDOS RECUBIERTOS CON PELICULA — Description, Dosage, Side Effects | PillsCard
OTC
TAGRISSO 40 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
INN: TAGRISSO
Data updated: 2026-04-11
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About This Product
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Astrazeneca Ab (ES)
Source
CIMA_ES
(
ARTG
)
TAGRISSO as monotherapy is indicated:, as adjuvant therapy after tumour resection in patients with non-small cell lung cancer (NSCLC) whose tumours have activating epidermal growth factor receptor (EGFR) mutations, as detected by a validated test., the treatment of patients with locally advanced, unresectable (stage III) NSCLC whose tumours have activating EGFR mutations and whose disease has not progressed during or following platinum-based chemoradiation therapy., for the first-line treatment of patients with locally advanced or metastatic NSCLC whose tumours have activating EGFR mutations, as detected by a validated test., for the treatment of patients with locally advanced or metastatic NSCLC that is EGFR T790M mutation-positive, as detected by a validated test.,TAGRISSO is indicated in combination with:, pemetrexed and platinum-based chemotherapy for the first-line treatment of patients with locally advanced or metastatic NSCLC whose tumours have EGFR exon 19 deletions or exon 21 L858R mutations.TAGRISSO as monotherapy is indicated:
as adjuvant therapy after tumour resection in patients with non-small cell lung cancer (NSCLC) whose tumours have activating epidermal growth factor receptor (EGFR) mutations, as detected by a validated test.
for the first-line treatment of patients with locally advanced or metastatic NSCLC whose tumours have activating EGFR mutations, as detected by a validated test.
for the treatment of patients with locally advanced or metastatic NSCLC that is EGFR T790M mutation-positive, as detected by a validated test.
TAGRISSO is indicated in combination with:
pemetrexed and platinum-based chemotherapy for the first-line treatment of patients with locally advanced or metastatic NSCLC whose tumours have EGFR exon 19 deletions or exon 21 L858R mutations.