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warnings and cautions
5.4 Risk of Breakthrough Seizures Due to Drug Interaction with Valproic Acid The concomitant use of VABOMERE and valproic acid or divalproex sodium is generally not recommended. Case reports in the literature have shown that co-administration of carbapenems, including meropenem, to patients receiving valproic acid or divalproex sodium results in a reduction in valproic acid concentrations. The valproic acid concentrations may drop below the therapeutic range as a result of this interaction, therefore increasing the risk of breakthrough seizures. Increasing the dose of valproic acid or divalproex sodium may not be sufficient to overcome this interaction. Consider administration of antibacterial drugs other than carbapenems to treat infections in patients whose seizures are well controlled on valproic acid or divalproex sodium. If administration of VABOMERE is necessary, consider supplemental anticonvulsant therapy [see Drug Interactions ( 7.1 )] .
warnings and cautions
5.5 Thrombocytopenia In patients with renal impairment, thrombocytopenia has been observed in patients treated with meropenem, but no clinical bleeding has been reported [see Dosage and Administration ( 2.2 ), Adverse Reactions ( 6.1 ), Use in Specific Populations ( 8.5 ) and ( 8.6 ), and Clinical Pharmacology ( 12.3 ) ] .
warnings and cautions
5.6 Potential for Neuromotor Impairment Alert patients receiving VABOMERE on an outpatient basis regarding adverse reactions such as seizures, delirium, headaches and/or paresthesias that could interfere with mental alertness and/or cause motor impairment. Until it is reasonably well established that VABOMERE is well tolerated, advise patients not to operate machinery or motorized vehicles [see Adverse Reactions ( 6.1 )].
warnings and cautions
5.7 Development of Drug-Resistant Bacteria Prescribing VABOMERE in the absence of a proven or strongly suspected bacterial infection is unlikely to provide benefit to the patient and increases the risk of drug-resistant bacteria [see Indications and Usage ( 1.2 )] .
6 ADVERSE REACTIONS The following adverse reactions are discussed in greater detail in the Warnings and Precautions section: Hypersensitivity Reactions [see Warnings and Precautions ( 5.1 )] Seizure Potential [see Warnings and Precautions ( 5.2 )] Clostridium difficile -associated Diarrhea [see Warnings and Precautions ( 5.3 )] Risk of Breakthrough Seizures Due to Drug Interaction with Valproic Acid [see Warnings and Precautions ( 5.4 )] Thrombocytopenia [see Warnings and Precautions ( 5.5 )] Potential for Neuromotor Impairment [see Warnings and Precautions ( 5.6 )] Development of Drug-Resistant Bacteria [see Warnings and Precautions ( 5.7 )] Overgrowth of Nonsusceptible Organisms [see Warnings and Precautions ( 5.8 )] The most frequently reported adverse reactions occurring in ≥3% of patients treated with VABOMERE were headache, phlebitis/infusion site reactions, and diarrhea. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact The Medicines Company at 1-888-977-6326 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . See 17 for PATIENT COUNSELING INFORMATION 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. VABOMERE was evaluated in a Phase 3 comparator-controlled clinical trial in cUTI, including pyelonephritis, which included 272 patients treated with VABOMERE and 273 patients treated with the comparator piperacillin/tazobactam 4.5 grams (piperacillin 4 g/tazobactam 0.5 g) every 8 hours. After a minimum of 15 doses of IV therapy, patients could be switched to oral levofloxacin (500 mg daily every 24 hours) to complete the treatment course. Mean duration of IV therapy was 8 days in both treatment groups. Mean duration of IV and oral therapy was 10 days; patients with baseline bacteremia could receive up to 14 days of treatment. The mean age of patients treated with VABOMERE was 53 years (range 18 to 92 years), and 32% of patients were 65 years of age or older. Patients were predominantly female (66.5%) and White (93.4%). Most patients were enrolled in Europe (89.7%). Serious Adverse Reactions and Adverse Reactions Leading to Discontinuation Treatment was discontinued due to adverse reactions in 2.9% (8/272) of patients receiving VABOMERE and in 5.1% (14/273) of patients receiving piperacillin/tazobactam. Most common adverse reactions resulting in discontinuation of VABOMERE included hypersensitivity, 1.1% (3/272) and infusion-related reactions, 0.7% (2/272). Death occurred in 2 (0.7%) patients who received VABOMERE and in 2 (0.7%) patients who received piperacillin/tazobactam. Common Adverse Reactions The most frequently reported adverse reactions (3% or greater) in patients receiving VABOMERE in the Phase 3 cUTI trial were headache, phlebitis/infusion site reactions, and diarrhea. Table 3 provides adverse reactions occurring in 1% or greater of patients receiving VABOMERE in the Phase 3 cUTI trial. Table 3: Adverse Reactions Occurring in 1% or Greater of Patients Receiving VABOMERE in the Phase 3 Clinical Trial in cUTI Adverse Reactions VABOMERE (N=272) % Piperacillin/Tazobactama (N=273) % Headache 8.8 4.4 Phlebitis/Infusion site reactions b 4.4 0.7 Diarrhea 3.3 4.4 Hypersensitivity 1.8 1.8 Nausea 1.8 1.5 Alanine aminotransferase increased 1.8 0.4 Aspartate aminotransferase increased 1.5 0.7 Pyrexia 1.5 0.7 Hypokalemia 1.1 1.5 a Piperacillin/tazobactam 4.5 grams (piperacillin 4 g/tazobactam 0.5 g) IV infused over 30 minutes every 8 hours. b Infusion site reactions include infusion/injection site phlebitis, infusion site thrombosis, and infusion site erythema. c Hypersensitivity includes hypersensitivity, drug hypersensitivity, anaphylactic reaction, rash urticaria, and bronchospasm Adverse Reactions Occurring in Less Than 1% of Patients Receiving VABOMERE in the Phase 3 cUTI trial : Blood and lymphatic system disorders : leukopenia General disorders and administration site conditions : chest discomfort Infections and infestations : pharyngitis, vulvovaginal candidiasis, oral candidiasis Investigations : creatinine phosphokinase increase Metabolism and nutrition disorders : decreased appetite, hyperkalemia, hyperglycemia, hypoglycemia Nervous system disorders : dizziness, tremor, paresthesia, lethargy Psychiatric disorders : hallucination, insomnia Renal and urinary disorders : azotemia, renal impairment Vascular disorders : deep vein thrombosis, hypotension, vascular pain Other Adverse Reactions Associated with Meropenem Additionally, adverse reactions reported with meropenem alone that were not reported in VABOMERE-treated patients in the Phase 3 clinical trial are listed below: Blood and lymphatic system disorders : thrombocytosis, neutropenia, eosinophilia, thrombocytopenia, agranulocytosis, hemolytic anemia Gastrointestinal disorders : abdominal pain Hepatobiliary disorders : jaundice Nervous system disorders : convulsions Investigations : blood alkaline phosphatase increased, blood lactate dehydrogenase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, blood thromboplastin decreased, prothrombin time decreased, Direct and Indirect Coombs test positive Skin and subcutaneous tissue disorders : pruritus, toxic epidermal necrolysis, Stevens Johnson syndrome, Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome, erythema multiforme Immune system disorders : angioedema General disorders and administration site conditions : pain
adverse reactions
6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. VABOMERE was evaluated in a Phase 3 comparator-controlled clinical trial in cUTI, including pyelonephritis, which included 272 patients treated with VABOMERE and 273 patients treated with the comparator piperacillin/tazobactam 4.5 grams (piperacillin 4 g/tazobactam 0.5 g) every 8 hours. After a minimum of 15 doses of IV therapy, patients could be switched to oral levofloxacin (500 mg daily every 24 hours) to complete the treatment course. Mean duration of IV therapy was 8 days in both treatment groups. Mean duration of IV and oral therapy was 10 days; patients with baseline bacteremia could receive up to 14 days of treatment. The mean age of patients treated with VABOMERE was 53 years (range 18 to 92 years), and 32% of patients were 65 years of age or older. Patients were predominantly female (66.5%) and White (93.4%). Most patients were enrolled in Europe (89.7%). Serious Adverse Reactions and Adverse Reactions Leading to Discontinuation Treatment was discontinued due to adverse reactions in 2.9% (8/272) of patients receiving VABOMERE and in 5.1% (14/273) of patients receiving piperacillin/tazobactam. Most common adverse reactions resulting in discontinuation of VABOMERE included hypersensitivity, 1.1% (3/272) and infusion-related reactions, 0.7% (2/272). Death occurred in 2 (0.7%) patients who received VABOMERE and in 2 (0.7%) patients who received piperacillin/tazobactam. Common Adverse Reactions The most frequently reported adverse reactions (3% or greater) in patients receiving VABOMERE in the Phase 3 cUTI trial were headache, phlebitis/infusion site reactions, and diarrhea. Table 3 provides adverse reactions occurring in 1% or greater of patients receiving VABOMERE in the Phase 3 cUTI trial. Table 3: Adverse Reactions Occurring in 1% or Greater of Patients Receiving VABOMERE in the Phase 3 Clinical Trial in cUTI Adverse Reactions VABOMERE (N=272) % Piperacillin/Tazobactama (N=273) % Headache 8.8 4.4 Phlebitis/Infusion site reactions b 4.4 0.7 Diarrhea 3.3 4.4 Hypersensitivity 1.8 1.8 Nausea 1.8 1.5 Alanine aminotransferase increased 1.8 0.4 Aspartate aminotransferase increased 1.5 0.7 Pyrexia 1.5 0.7 Hypokalemia 1.1 1.5 a Piperacillin/tazobactam 4.5 grams (piperacillin 4 g/tazobactam 0.5 g) IV infused over 30 minutes every 8 hours. b Infusion site reactions include infusion/injection site phlebitis, infusion site thrombosis, and infusion site erythema. c Hypersensitivity includes hypersensitivity, drug hypersensitivity, anaphylactic reaction, rash urticaria, and bronchospasm Adverse Reactions Occurring in Less Than 1% of Patients Receiving VABOMERE in the Phase 3 cUTI trial : Blood and lymphatic system disorders : leukopenia General disorders and administration site conditions : chest discomfort Infections and infestations : pharyngitis, vulvovaginal candidiasis, oral candidiasis Investigations : creatinine phosphokinase increase Metabolism and nutrition disorders : decreased appetite, hyperkalemia, hyperglycemia, hypoglycemia Nervous system disorders : dizziness, tremor, paresthesia, lethargy Psychiatric disorders : hallucination, insomnia Renal and urinary disorders : azotemia, renal impairment Vascular disorders : deep vein thrombosis, hypotension, vascular pain Other Adverse Reactions Associated with Meropenem Additionally, adverse reactions reported with meropenem alone that were not reported in VABOMERE-treated patients in the Phase 3 clinical trial are listed below: Blood and lymphatic system disorders : thrombocytosis, neutropenia, eosinophilia, thrombocytopenia, agranulocytosis, hemolytic anemia Gastrointestinal disorders : abdominal pain Hepatobiliary disorders : jaundice Nervous system disorders : convulsions Investigations : blood alkaline phosphatase increased, blood lactate dehydrogenase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, blood thromboplastin decreased, prothrombin time decreased, Direct and Indirect Coombs test positive Skin and subcutaneous tissue disorders : pruritus, toxic epidermal necrolysis, Stevens Johnson syndrome, Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome, erythema multiforme Immune system disorders : angioedema General disorders and administration site conditions : pain